TIP maker and TIP marker; EB1 as a master controller of microtubule pl
http://www.100md.com
《细胞学杂志》
Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556
Correspondence to Kevin T. Vaughan: Vaughan.4@nd.edu
Abstract
The EB1 protein is a member of the exciting and enigmatic family of microtubule (MT) tip-tracking proteins. EB1 acts as an exquisite marker of dynamic MT plus ends in some cases, whereas in others EB1 is thought to directly dictate the behavior of the plus ends. How EB1 differentiates between these two roles remains unclear; however, a growing list of interactions between EB1 and other MT binding proteins suggests there may be a single mechanism. Adding another layer of complexity to these interactions, two studies published in this issue implicate EB1 in cross-talk between mitotic MTs and between MTs and actin filaments (Goshima et al., p. 229; Wu et al., p. 201). These results raise the possibility that EB1 is a central player in MT-based transport, and that the activity of MT-binding proteins depends on their ability or inability to interact with EB1.
Abbreviations used in this paper: APC, adenomatous polyposis coli; C-MT, centrosomal MT; K-fibers, kinetochore fibers; MT, microtubule; siRNA, small interfering RNA.
EB1 is a MT tip-tracking protein
EB1 was first described as an adenomatous polyposis coli (APC)–interacting protein whose binding domain was affected by APC mutations implicated in colon cancer (Su et al., 1995). Subsequent localization revealed that EB1 binds to and labels a subset of the total microtubule (MT) population and that it displays some preference for the very plus end of these MTs (Morrison et al., 1998). Live-cell imaging of transfected GFP fusion proteins further revealed specificity for the tips of MTs undergoing elongation (Mimori-Kiyosue et al., 2000). This tendency to bind elongating MT plus ends and to appear to "track" with these ends as long as they extend is known as "tip tracking," and an impressive number of MT-binding proteins display this tip-tracking activity in live-cell imaging assays (for review see Vaughan, 2004). In most cases, high resolution imaging suggests that these proteins "treadmill" at the elongating plus ends rather than translocate or "surf" with the growing tip. This contrasts, to some extent, the behavior of homologues in yeast and filamentous fungi that appear to translocate toward the plus end via a kinesin motor or other mechanisms (Xiang et al., 2000; Liakopoulos et al., 2003). In mammalian cells, tip tracking is best characterized in transfection assays where fluorescent fusion proteins are overexpressed at some level. Often the degree of tip specificity is influenced by the amount of expressed protein. Although tip specificity is evident at low levels of expression, a transition to decoration along the length of MTs becomes prominent as the level of expression increases. For some tip trackers, this tendency is thought to reflect a regulatory cycle at the MT plus end (Vaughan et al., 2002). However, MTs can tolerate high levels of EB1 better than the other tip trackers, suggesting something unique and intriguing about EB1.
Tip tracking and EB1 function
Despite an explosion of recent work on EB1, the precise function and location of endogenous EB1 at native levels remains unclear. The MT-associated population of EB1 represents a small subset of total EB1, but this subset has received the most attention. The remainder is thought to be largely soluble, similar to the form that dominates the GFP-EB1 expression studies. Immunofluorescence microscopy images suggest that native EB1 is punctate, resembling vesicles or large protein complexes (Morrison et al., 1998; Faulkner et al., 2000; Mimori-Kiyosue et al., 2000). This would be consistent with the extensive colocalization with other membrane-associated proteins such as CLIP-170 and dynactin. However, nonmembranous protein complexes including binding partners such at APC are also described, and the function of these is under investigation (Mimori-Kiyosue et al., 2000; Wen et al., 2004). In these settings, direct interactions between EB1 and other proteins (p150Glued, CLIP-170, and CLASPs) have been interpreted as recruitment mechanisms (Fig. 1). The fact that these binding partners can also bind tubulin directly suggests some transition or sequential loading process at plus ends that will require more work to resolve.
Figure 1. Functions for EB1 during interphase and mitosis. GFP-EB1 labels MT plus ends at multiple cellular sites where MT search-capture occurs. (A) EB1 has been implicated in search-capture of ER-Golgi transport vesicles and in MT capture at the cell cortex during cytoskeletal reorientation. In these cases, EB1 highlights locations where search-capture is in progress or has identified capture sites. (B) EB1 has also been linked to search-capture sites during mitosis including the kinetochores of chromosomes during prometaphase and locations at the cell cortex where astral MTs can attach. Depletion of EB1 has been shown to induce short MTs that fail to reach the cell cortex. The consequences include mis-orientation of the spindle.
Related to the recruitment function of EB1, another model is focused on the ability of EB1 to regulate MT growth. A series of elegant biochemical, immunodepletion, and small interfering RNA (siRNA)/rescue assays indicate that EB1 can stimulate growth at MT plus ends (Fig. 1) and that this is critical in situations where search-capture requires long and dynamic MTs (Tirnauer and Bierer, 2000; Rogers et al., 2002; Tirnauer et al., 2002b; Ligon et al., 2003). Current limitations make it difficult to define how EB1 arrives at the MT plus end, but the substantial soluble pool and the ability to add soluble EB1 experimentally suggests it either coassembles with the elongating MT tip or is recruited soon after tubulin polymer is exposed.
New tip trackers suggest additional roles for EB1
In this issue, Wu et al. (p. 201) expand the list of tip trackers to include melanophillin, which is recognized as a linker between the myosin V motor and Rab 27a required for myosin-driven transport of melanosomes in pigmented cells (Wu et al., 2002). MT-based transport is also an essential component of melanosome delivery in pigmented cells (Rogers et al., 1997), and the mechanisms that allow transfer of melanosomes from the MT network to microfilaments have been unclear. Using overexpression of fluorochrome-tagged melanophillin, Wu et al. (2005) report robust tip tracking of the expressed protein and demonstrate that this behavior requires EB1. This association of melanophillin with EB1 does not require either myosin V or rab27a, because tip tracking is evident in melanocytes from ashen and dilute mice, and interaction-disrupting melanophillin mutants tip-track as well. Although melanophillin depends on EB1 for MT binding, EB1 does not appear to require melanophillin for normal function. Only a subset of EB1 comets contains detectable melanophillin in melanocytes, and EB1 is expressed in many cell types that do not express melanophillin.
The conceptual challenge of this work is to determine the function of EB1 and MT binding for melanophillin. Is this a nuance of overexpression or an important clue into the role melanophillin plays in melanosome transport? Interestingly, the authors point out that melanosomes do not tip-track normally, and that the movements of melanosomes are very different from tip-tracking proteins. Furthermore, expression of the tagged melanophillin constructs reveals both MT- and actin-associated structures in the cell periphery. Perhaps this dichotomy is the crucial finding for melanophillin. The authors propose the enticing possibility that melanophillin uses a combination of MT binding (via EB1) and actin binding (via myosin V) to build a transient transfer station in the cell periphery where melanosomes can be efficiently handed from MTs to microfilaments (Fig. 2). This is consistent with the known behaviors of melanosomes (Rogers and Gelfand, 1998) and uncovers a functional aspect of melanophillin that would be difficult to examine due to the transient nature of these intermediates. In common with other EB1 studies, it remains unclear if EB1 serves a role as a marker for MT plus ends that have reached the cell periphery, or if EB1 actively preserves particular MT plus ends long enough to allow the hand-off. However, this work provides compelling evidence that EB1 plays a larger role than previously anticipated.
Figure 2. EB1 as a multi-functional protein involved in cargo transfer. Models proposed by studies in this issue (Goshima et al., 2005; Wu et al., 2005) suggest a more global role for EB1 in cytoskeletal transport. (A) MT tip tracking of melanophillin in an EB1-dependent manner coupled with binding of melanophillin to myosin Va in melanocytes identifies a new function for EB1. In contrast to other models that implicate EB1 in recruitment of proteins involved in MT-based transport, this work potentially identifies a role in transfer of cargo from one cytoskeletal system to another (MTs to actin). (B) Parallel work on MT motors involved in mitotic spindle formation identify a connection between EB1 and ncd at sites where kinetochore fibers (k-fibers) interact with centrosomal MTs (C-MTs) emanating from the spindle poles. EB1 is proposed to play a role in determining where ncd initiates contact between these two MT populations—a role that molecular modeling predicts is essential for the formation of a functional and focused spindle.
Adding further weight to the possibility that EB1 coordinates transfer between cytoskeletal systems, this issue also includes a study from Goshima et al. (p. 229) that reports a new role for EB1 in mitotic spindle function. Using Drosophila S2 cells as a model together with siRNA-driven depletion, this group dissects the contribution of ncd and cytoplasmic dynein in the formation and motility of kinetochore-linked (K-fibers) and centrosome-linked (C-MTs) MT bundles during spindle pole focusing. Depletion of cytoplasmic dynein primarily impacted the ability of K-fibers to move toward the spindle poles, whereas depletion of ncd affected the focusing of the k-fibers into a tight spindle. Although these motors share some functional redundancy, time-lapse sequences highlight the phenotypic distinction between k-fiber focusing and transport.
To better understand the specific function of each motor, imaging of ncd-GFP was accomplished through depletion of endogenous ncd by siRNA coupled with expression of ncd-GFP. Focusing on cells with almost normal levels of functional ncd, Goshima et al. (2005) report accumulation of ncd-GFP at spindle poles and along K-fibers. This finding is consistent with the bivalent nature of ncd-MT interactions, potentially playing a role in MT cross-linking in the spindle. However, FRAP analysis revealed that ncd-GFP is highly dynamic on these MTs and displays enrichment at the plus ends of MTs emanating from the spindle poles similar to tip tracking. Expression of ncd-GFP during interphase also revealed tip tracking, adding ncd to the list of plus end–binding proteins. Although it was unclear how ncd (a minus end–directed motor) would target to plus ends, previous work on EB1 (Rogers et al., 2002, 2004) suggested a mechanism. siRNA-mediated depletion of EB1 induced a transition from tip-specific binding to more uniform labeling of MTs. This was coupled with a reduction in MT dynamics that correlated with a loss of K-fiber focusing similar to ncd depletion.
As a tool to predict how MT plus end binding of ncd could contribute to K-fiber focusing, Goshima et al. (2005) use molecular modeling of a minimal spindle and compare the outcomes of two scenarios. The first scenario assumes that an ncd–EB1 complex targets the motor domain of ncd to K-fibers and the tail of ncd (NH2-terminus) to the plus ends of C-MTs via the EB1 interaction. The second scenario has the opposite orientation with the ncd motor binding C-MTs and the tail binding K-fibers via EB1. Simulations support the second model with the ncd motor associating with the plus ends of C-MTs and moving toward the poles (Fig. 2). In this arrangement, the ncd tail and EB1 attach to K-fibers, allowing ncd to draw the K-fibers toward the poles. Given the proposed role of EB1 in imparting plus end specificity to ncd, this outcome is somewhat counterintuitive. However, EB1 could contribute by ensuring that the K-fiber/ncd/C-MT interaction occurs only at the plus ends of C-MTs. Similar to the melanophillin story above, EB1 could represent a marker for transient interactions between distinct filament systems.
Insights into EB1 function
Although the studies of melanophillin and ncd reported in this issue appear to focus on very different questions, the overlapping contributions of EB1 to both stories suggests a fundamentally new model for EB1 function and the potential role of tip tracking. If one adds the other locations where EB1 is thought to function, a theme emerges that supports a more central role for EB1 in interactions between large multi-subunit complexes. Although not completely understood, in interphase cells MT plus ends contain EB1 and other tip-trackers where they appear to mark locations of search-capture between MTs and membranes (Pierre et al., 1992; Valetti et al., 1999; Vaughan et al., 2002; Wen et al., 2004). An overlapping class of EB1-associated proteins are found at kinetochores during prometaphase where search-capture of chromosomes occurs (Dujardin et al., 1998; Faulkner et al., 2000; Tirnauer et al., 2002a). If we add transfer of melanosomes from MTs to actin filaments (Wu et al., 2005) and linkage of K-fibers and C-MTs (Goshima et al., 2005) to the list, one could propose that EB1 is the master integrator of protein complex assembly on MTs. It remains unclear if this function is related to the impression conveyed by tip-tracking assays, or if tip tracking simply reflects the fact that EB1–MT interactions are tightly regulated (Vaughan, 2004). Future work and the identification of new EB1-binding partners will shed light on this intriguing question.
Conclusion
The growing list of EB1-interacting proteins and functions suggests that our understanding of EB1 and MT tip tracking is incomplete. The addition of two new candidates to the plus end–binding protein family implies that EB1 plays a fundamental role in coordinating movement along MTs by defining locations where specific conditions have been met for transport. This model represents a conceptual advance for analysis of tip-tracking proteins and provides the framework for further dissection of their function.
Acknowledgments
The author thanks Edward Hinchcliffe (University of Notre Dame) for helpful comments. Space limitations prevent the citation of additional EB1 studies that contribute to our understanding of EB1 function.
This work was supported by funding from National Institutes of Health (grant GM60560) and the American Cancer Society.
References
Dujardin, D., U.I. Wacker, A. Moreau, T.A. Schroer, J.E. Rickard, and J.R. De Mey. 1998. Evidence for a role of CLIP-170 in the establishment of metaphase chromosome alignment. J. Cell Biol. 141:849–862.
Faulkner, N.E., D.L. Dujardin, C.Y. Tai, K.T. Vaughan, C.B. O'Connell, Y. Wang, and R.B. Vallee. 2000. A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function. Nat. Cell Biol. 2:784–791.
Goshima, G., F. Nedelec, and R.D. Vale. 2005. Mechanisms for focusing mitotic spindle poles by minus end–directed motor proteins. J Cell Biol. 171:229–240.
Liakopoulos, D., J. Kusch, S. Grava, J. Vogel, and Y. Barral. 2003. Asymmetric loading of Kar9 onto spindle poles and microtubules ensures proper spindle alignment. Cell. 112:561–574.
Ligon, L.A., S.S. Shelly, M. Tokito, and E.L. Holzbaur. 2003. The microtubule plus-end proteins EB1 and dynactin have differential effects on microtubule polymerization. Mol. Biol. Cell. 14:1405–1417.
Mimori-Kiyosue, Y., N. Shiina, and S. Tsukita. 2000. The dynamic behavior of the APC-binding protein EB1 on the distal ends of microtubules. Curr. Biol. 10:865–868.
Morrison, E.E., B.N. Wardleworth, J.M. Askham, A.F. Markham, and D.M. Meredith. 1998. EB1, a protein which interacts with the APC tumour suppressor, is associated with the microtubule cytoskeleton throughout the cell cycle. Oncogene. 17:3471–3477.
Pierre, P., J. Scheel, J.E. Rickard, and T.E. Kreis. 1992. CLIP-170 links endocytic vesicles to microtubules. Cell. 70:887–900.
Rogers, S.L., and V.I. Gelfand. 1998. Myosin cooperates with microtubule motors during organelle transport in melanophores. Curr. Biol. 8:161–164.
Rogers, S.L., I.S. Tint, P.C. Fanapour, and V.I. Gelfand. 1997. Regulated bidirectional motility of melanophore pigment granules along microtubules in vitro. Proc. Natl. Acad. Sci. USA. 94:3720–3725.
Rogers, S.L., G.C. Rogers, D.J. Sharp, and R.D. Vale. 2002. Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle. J. Cell Biol. 158:873–884.
Rogers, S.L., U. Wiedemann, U. Hacker, C. Turck, and R.D. Vale. 2004. Drosophila RhoGEF2 associates with microtubule plus ends in an EB1-dependent manner. Curr. Biol. 14:1827–1833.
Su, L.K., M. Burrell, D.E. Hill, J. Gyuris, R. Brent, R. Wiltshire, J. Trent, B. Vogelstein, and K.W. Kinzler. 1995. APC binds to the novel protein EB1. Cancer Res. 55:2972–2977.
Tirnauer, J.S., and B.E. Bierer. 2000. EB1 proteins regulate microtubule dynamics, cell polarity, and chromosome stability. J. Cell Biol. 149:761–766.
Tirnauer, J.S., J.C. Canman, E.D. Salmon, and T.J. Mitchison. 2002a. EB1 targets to kinetochores with attached, polymerizing microtubules. Mol. Biol. Cell. 13:4308–4316.
Tirnauer, J.S., S. Grego, E.D. Salmon, and T.J. Mitchison. 2002b. EB1-microtubule interactions in Xenopus egg extracts: role of EB1 in microtubule stabilization and mechanisms of targeting to microtubules. Mol. Biol. Cell. 13:3614–3626.
Valetti, C., D.M. Wetzel, M. Schrader, M.J. Hasbani, S.R. Gill, T.E. Kreis, and T.A. Schroer. 1999. Role of dynactin in endocytic traffic: effects of dynamitin overexpression and colocalization with CLIP-170. Mol. Biol. Cell. 10:4107–4120.
Vaughan, K.T. 2004. Surfing, regulating and capturing: are all microtubule-tip-tracking proteins created equal? Trends Cell Biol. 14:491–496.
Vaughan, P.S., P. Miura, M. Henderson, B. Byrne, and K.T. Vaughan. 2002. A role for regulated binding of p150Glued to microtubule plus ends in organelle transport. J. Cell Biol. 158:305–319
Wen, Y., C.H. Eng, J. Schmoranzer, N. Cabrera-Poch, E.J. Morris, M. Chen, B.J. Wallar, A.S. Alberts, and G.G. Gundersen. 2004. EB1 and APC bind to mDia to stabilize microtubules downstream of Rho and promote cell migration. Nat. Cell Biol. 6:820–830.
Wu, X., G.L. Tsan, and J.A. Hammer. 2005. Melanophillin and myosin Va track the microtubule plus end on EB1. J. Cell Biol. 171:201–207.
Wu, X.S., K. Rao, H. Zhang, F. Wang, J.R. Sellers, L.E. Matesic, N.G. Copeland, N.A. Jenkins, and J.A. Hammer III. 2002. Identification of an organelle receptor for myosin-Va. Nat. Cell Biol. 4:271–278.
Xiang, X., G. Han, D.A. Winkelmann, W. Zuo, and N.R. Morris. 2000. Dynamics of cytoplasmic dynein in living cells and the effect of a mutation in the dynactin complex actin-related protein Arp1. Curr. Biol. 10:603–606.(Kevin T. Vaughan)
Correspondence to Kevin T. Vaughan: Vaughan.4@nd.edu
Abstract
The EB1 protein is a member of the exciting and enigmatic family of microtubule (MT) tip-tracking proteins. EB1 acts as an exquisite marker of dynamic MT plus ends in some cases, whereas in others EB1 is thought to directly dictate the behavior of the plus ends. How EB1 differentiates between these two roles remains unclear; however, a growing list of interactions between EB1 and other MT binding proteins suggests there may be a single mechanism. Adding another layer of complexity to these interactions, two studies published in this issue implicate EB1 in cross-talk between mitotic MTs and between MTs and actin filaments (Goshima et al., p. 229; Wu et al., p. 201). These results raise the possibility that EB1 is a central player in MT-based transport, and that the activity of MT-binding proteins depends on their ability or inability to interact with EB1.
Abbreviations used in this paper: APC, adenomatous polyposis coli; C-MT, centrosomal MT; K-fibers, kinetochore fibers; MT, microtubule; siRNA, small interfering RNA.
EB1 is a MT tip-tracking protein
EB1 was first described as an adenomatous polyposis coli (APC)–interacting protein whose binding domain was affected by APC mutations implicated in colon cancer (Su et al., 1995). Subsequent localization revealed that EB1 binds to and labels a subset of the total microtubule (MT) population and that it displays some preference for the very plus end of these MTs (Morrison et al., 1998). Live-cell imaging of transfected GFP fusion proteins further revealed specificity for the tips of MTs undergoing elongation (Mimori-Kiyosue et al., 2000). This tendency to bind elongating MT plus ends and to appear to "track" with these ends as long as they extend is known as "tip tracking," and an impressive number of MT-binding proteins display this tip-tracking activity in live-cell imaging assays (for review see Vaughan, 2004). In most cases, high resolution imaging suggests that these proteins "treadmill" at the elongating plus ends rather than translocate or "surf" with the growing tip. This contrasts, to some extent, the behavior of homologues in yeast and filamentous fungi that appear to translocate toward the plus end via a kinesin motor or other mechanisms (Xiang et al., 2000; Liakopoulos et al., 2003). In mammalian cells, tip tracking is best characterized in transfection assays where fluorescent fusion proteins are overexpressed at some level. Often the degree of tip specificity is influenced by the amount of expressed protein. Although tip specificity is evident at low levels of expression, a transition to decoration along the length of MTs becomes prominent as the level of expression increases. For some tip trackers, this tendency is thought to reflect a regulatory cycle at the MT plus end (Vaughan et al., 2002). However, MTs can tolerate high levels of EB1 better than the other tip trackers, suggesting something unique and intriguing about EB1.
Tip tracking and EB1 function
Despite an explosion of recent work on EB1, the precise function and location of endogenous EB1 at native levels remains unclear. The MT-associated population of EB1 represents a small subset of total EB1, but this subset has received the most attention. The remainder is thought to be largely soluble, similar to the form that dominates the GFP-EB1 expression studies. Immunofluorescence microscopy images suggest that native EB1 is punctate, resembling vesicles or large protein complexes (Morrison et al., 1998; Faulkner et al., 2000; Mimori-Kiyosue et al., 2000). This would be consistent with the extensive colocalization with other membrane-associated proteins such as CLIP-170 and dynactin. However, nonmembranous protein complexes including binding partners such at APC are also described, and the function of these is under investigation (Mimori-Kiyosue et al., 2000; Wen et al., 2004). In these settings, direct interactions between EB1 and other proteins (p150Glued, CLIP-170, and CLASPs) have been interpreted as recruitment mechanisms (Fig. 1). The fact that these binding partners can also bind tubulin directly suggests some transition or sequential loading process at plus ends that will require more work to resolve.
Figure 1. Functions for EB1 during interphase and mitosis. GFP-EB1 labels MT plus ends at multiple cellular sites where MT search-capture occurs. (A) EB1 has been implicated in search-capture of ER-Golgi transport vesicles and in MT capture at the cell cortex during cytoskeletal reorientation. In these cases, EB1 highlights locations where search-capture is in progress or has identified capture sites. (B) EB1 has also been linked to search-capture sites during mitosis including the kinetochores of chromosomes during prometaphase and locations at the cell cortex where astral MTs can attach. Depletion of EB1 has been shown to induce short MTs that fail to reach the cell cortex. The consequences include mis-orientation of the spindle.
Related to the recruitment function of EB1, another model is focused on the ability of EB1 to regulate MT growth. A series of elegant biochemical, immunodepletion, and small interfering RNA (siRNA)/rescue assays indicate that EB1 can stimulate growth at MT plus ends (Fig. 1) and that this is critical in situations where search-capture requires long and dynamic MTs (Tirnauer and Bierer, 2000; Rogers et al., 2002; Tirnauer et al., 2002b; Ligon et al., 2003). Current limitations make it difficult to define how EB1 arrives at the MT plus end, but the substantial soluble pool and the ability to add soluble EB1 experimentally suggests it either coassembles with the elongating MT tip or is recruited soon after tubulin polymer is exposed.
New tip trackers suggest additional roles for EB1
In this issue, Wu et al. (p. 201) expand the list of tip trackers to include melanophillin, which is recognized as a linker between the myosin V motor and Rab 27a required for myosin-driven transport of melanosomes in pigmented cells (Wu et al., 2002). MT-based transport is also an essential component of melanosome delivery in pigmented cells (Rogers et al., 1997), and the mechanisms that allow transfer of melanosomes from the MT network to microfilaments have been unclear. Using overexpression of fluorochrome-tagged melanophillin, Wu et al. (2005) report robust tip tracking of the expressed protein and demonstrate that this behavior requires EB1. This association of melanophillin with EB1 does not require either myosin V or rab27a, because tip tracking is evident in melanocytes from ashen and dilute mice, and interaction-disrupting melanophillin mutants tip-track as well. Although melanophillin depends on EB1 for MT binding, EB1 does not appear to require melanophillin for normal function. Only a subset of EB1 comets contains detectable melanophillin in melanocytes, and EB1 is expressed in many cell types that do not express melanophillin.
The conceptual challenge of this work is to determine the function of EB1 and MT binding for melanophillin. Is this a nuance of overexpression or an important clue into the role melanophillin plays in melanosome transport? Interestingly, the authors point out that melanosomes do not tip-track normally, and that the movements of melanosomes are very different from tip-tracking proteins. Furthermore, expression of the tagged melanophillin constructs reveals both MT- and actin-associated structures in the cell periphery. Perhaps this dichotomy is the crucial finding for melanophillin. The authors propose the enticing possibility that melanophillin uses a combination of MT binding (via EB1) and actin binding (via myosin V) to build a transient transfer station in the cell periphery where melanosomes can be efficiently handed from MTs to microfilaments (Fig. 2). This is consistent with the known behaviors of melanosomes (Rogers and Gelfand, 1998) and uncovers a functional aspect of melanophillin that would be difficult to examine due to the transient nature of these intermediates. In common with other EB1 studies, it remains unclear if EB1 serves a role as a marker for MT plus ends that have reached the cell periphery, or if EB1 actively preserves particular MT plus ends long enough to allow the hand-off. However, this work provides compelling evidence that EB1 plays a larger role than previously anticipated.
Figure 2. EB1 as a multi-functional protein involved in cargo transfer. Models proposed by studies in this issue (Goshima et al., 2005; Wu et al., 2005) suggest a more global role for EB1 in cytoskeletal transport. (A) MT tip tracking of melanophillin in an EB1-dependent manner coupled with binding of melanophillin to myosin Va in melanocytes identifies a new function for EB1. In contrast to other models that implicate EB1 in recruitment of proteins involved in MT-based transport, this work potentially identifies a role in transfer of cargo from one cytoskeletal system to another (MTs to actin). (B) Parallel work on MT motors involved in mitotic spindle formation identify a connection between EB1 and ncd at sites where kinetochore fibers (k-fibers) interact with centrosomal MTs (C-MTs) emanating from the spindle poles. EB1 is proposed to play a role in determining where ncd initiates contact between these two MT populations—a role that molecular modeling predicts is essential for the formation of a functional and focused spindle.
Adding further weight to the possibility that EB1 coordinates transfer between cytoskeletal systems, this issue also includes a study from Goshima et al. (p. 229) that reports a new role for EB1 in mitotic spindle function. Using Drosophila S2 cells as a model together with siRNA-driven depletion, this group dissects the contribution of ncd and cytoplasmic dynein in the formation and motility of kinetochore-linked (K-fibers) and centrosome-linked (C-MTs) MT bundles during spindle pole focusing. Depletion of cytoplasmic dynein primarily impacted the ability of K-fibers to move toward the spindle poles, whereas depletion of ncd affected the focusing of the k-fibers into a tight spindle. Although these motors share some functional redundancy, time-lapse sequences highlight the phenotypic distinction between k-fiber focusing and transport.
To better understand the specific function of each motor, imaging of ncd-GFP was accomplished through depletion of endogenous ncd by siRNA coupled with expression of ncd-GFP. Focusing on cells with almost normal levels of functional ncd, Goshima et al. (2005) report accumulation of ncd-GFP at spindle poles and along K-fibers. This finding is consistent with the bivalent nature of ncd-MT interactions, potentially playing a role in MT cross-linking in the spindle. However, FRAP analysis revealed that ncd-GFP is highly dynamic on these MTs and displays enrichment at the plus ends of MTs emanating from the spindle poles similar to tip tracking. Expression of ncd-GFP during interphase also revealed tip tracking, adding ncd to the list of plus end–binding proteins. Although it was unclear how ncd (a minus end–directed motor) would target to plus ends, previous work on EB1 (Rogers et al., 2002, 2004) suggested a mechanism. siRNA-mediated depletion of EB1 induced a transition from tip-specific binding to more uniform labeling of MTs. This was coupled with a reduction in MT dynamics that correlated with a loss of K-fiber focusing similar to ncd depletion.
As a tool to predict how MT plus end binding of ncd could contribute to K-fiber focusing, Goshima et al. (2005) use molecular modeling of a minimal spindle and compare the outcomes of two scenarios. The first scenario assumes that an ncd–EB1 complex targets the motor domain of ncd to K-fibers and the tail of ncd (NH2-terminus) to the plus ends of C-MTs via the EB1 interaction. The second scenario has the opposite orientation with the ncd motor binding C-MTs and the tail binding K-fibers via EB1. Simulations support the second model with the ncd motor associating with the plus ends of C-MTs and moving toward the poles (Fig. 2). In this arrangement, the ncd tail and EB1 attach to K-fibers, allowing ncd to draw the K-fibers toward the poles. Given the proposed role of EB1 in imparting plus end specificity to ncd, this outcome is somewhat counterintuitive. However, EB1 could contribute by ensuring that the K-fiber/ncd/C-MT interaction occurs only at the plus ends of C-MTs. Similar to the melanophillin story above, EB1 could represent a marker for transient interactions between distinct filament systems.
Insights into EB1 function
Although the studies of melanophillin and ncd reported in this issue appear to focus on very different questions, the overlapping contributions of EB1 to both stories suggests a fundamentally new model for EB1 function and the potential role of tip tracking. If one adds the other locations where EB1 is thought to function, a theme emerges that supports a more central role for EB1 in interactions between large multi-subunit complexes. Although not completely understood, in interphase cells MT plus ends contain EB1 and other tip-trackers where they appear to mark locations of search-capture between MTs and membranes (Pierre et al., 1992; Valetti et al., 1999; Vaughan et al., 2002; Wen et al., 2004). An overlapping class of EB1-associated proteins are found at kinetochores during prometaphase where search-capture of chromosomes occurs (Dujardin et al., 1998; Faulkner et al., 2000; Tirnauer et al., 2002a). If we add transfer of melanosomes from MTs to actin filaments (Wu et al., 2005) and linkage of K-fibers and C-MTs (Goshima et al., 2005) to the list, one could propose that EB1 is the master integrator of protein complex assembly on MTs. It remains unclear if this function is related to the impression conveyed by tip-tracking assays, or if tip tracking simply reflects the fact that EB1–MT interactions are tightly regulated (Vaughan, 2004). Future work and the identification of new EB1-binding partners will shed light on this intriguing question.
Conclusion
The growing list of EB1-interacting proteins and functions suggests that our understanding of EB1 and MT tip tracking is incomplete. The addition of two new candidates to the plus end–binding protein family implies that EB1 plays a fundamental role in coordinating movement along MTs by defining locations where specific conditions have been met for transport. This model represents a conceptual advance for analysis of tip-tracking proteins and provides the framework for further dissection of their function.
Acknowledgments
The author thanks Edward Hinchcliffe (University of Notre Dame) for helpful comments. Space limitations prevent the citation of additional EB1 studies that contribute to our understanding of EB1 function.
This work was supported by funding from National Institutes of Health (grant GM60560) and the American Cancer Society.
References
Dujardin, D., U.I. Wacker, A. Moreau, T.A. Schroer, J.E. Rickard, and J.R. De Mey. 1998. Evidence for a role of CLIP-170 in the establishment of metaphase chromosome alignment. J. Cell Biol. 141:849–862.
Faulkner, N.E., D.L. Dujardin, C.Y. Tai, K.T. Vaughan, C.B. O'Connell, Y. Wang, and R.B. Vallee. 2000. A role for the lissencephaly gene LIS1 in mitosis and cytoplasmic dynein function. Nat. Cell Biol. 2:784–791.
Goshima, G., F. Nedelec, and R.D. Vale. 2005. Mechanisms for focusing mitotic spindle poles by minus end–directed motor proteins. J Cell Biol. 171:229–240.
Liakopoulos, D., J. Kusch, S. Grava, J. Vogel, and Y. Barral. 2003. Asymmetric loading of Kar9 onto spindle poles and microtubules ensures proper spindle alignment. Cell. 112:561–574.
Ligon, L.A., S.S. Shelly, M. Tokito, and E.L. Holzbaur. 2003. The microtubule plus-end proteins EB1 and dynactin have differential effects on microtubule polymerization. Mol. Biol. Cell. 14:1405–1417.
Mimori-Kiyosue, Y., N. Shiina, and S. Tsukita. 2000. The dynamic behavior of the APC-binding protein EB1 on the distal ends of microtubules. Curr. Biol. 10:865–868.
Morrison, E.E., B.N. Wardleworth, J.M. Askham, A.F. Markham, and D.M. Meredith. 1998. EB1, a protein which interacts with the APC tumour suppressor, is associated with the microtubule cytoskeleton throughout the cell cycle. Oncogene. 17:3471–3477.
Pierre, P., J. Scheel, J.E. Rickard, and T.E. Kreis. 1992. CLIP-170 links endocytic vesicles to microtubules. Cell. 70:887–900.
Rogers, S.L., and V.I. Gelfand. 1998. Myosin cooperates with microtubule motors during organelle transport in melanophores. Curr. Biol. 8:161–164.
Rogers, S.L., I.S. Tint, P.C. Fanapour, and V.I. Gelfand. 1997. Regulated bidirectional motility of melanophore pigment granules along microtubules in vitro. Proc. Natl. Acad. Sci. USA. 94:3720–3725.
Rogers, S.L., G.C. Rogers, D.J. Sharp, and R.D. Vale. 2002. Drosophila EB1 is important for proper assembly, dynamics, and positioning of the mitotic spindle. J. Cell Biol. 158:873–884.
Rogers, S.L., U. Wiedemann, U. Hacker, C. Turck, and R.D. Vale. 2004. Drosophila RhoGEF2 associates with microtubule plus ends in an EB1-dependent manner. Curr. Biol. 14:1827–1833.
Su, L.K., M. Burrell, D.E. Hill, J. Gyuris, R. Brent, R. Wiltshire, J. Trent, B. Vogelstein, and K.W. Kinzler. 1995. APC binds to the novel protein EB1. Cancer Res. 55:2972–2977.
Tirnauer, J.S., and B.E. Bierer. 2000. EB1 proteins regulate microtubule dynamics, cell polarity, and chromosome stability. J. Cell Biol. 149:761–766.
Tirnauer, J.S., J.C. Canman, E.D. Salmon, and T.J. Mitchison. 2002a. EB1 targets to kinetochores with attached, polymerizing microtubules. Mol. Biol. Cell. 13:4308–4316.
Tirnauer, J.S., S. Grego, E.D. Salmon, and T.J. Mitchison. 2002b. EB1-microtubule interactions in Xenopus egg extracts: role of EB1 in microtubule stabilization and mechanisms of targeting to microtubules. Mol. Biol. Cell. 13:3614–3626.
Valetti, C., D.M. Wetzel, M. Schrader, M.J. Hasbani, S.R. Gill, T.E. Kreis, and T.A. Schroer. 1999. Role of dynactin in endocytic traffic: effects of dynamitin overexpression and colocalization with CLIP-170. Mol. Biol. Cell. 10:4107–4120.
Vaughan, K.T. 2004. Surfing, regulating and capturing: are all microtubule-tip-tracking proteins created equal? Trends Cell Biol. 14:491–496.
Vaughan, P.S., P. Miura, M. Henderson, B. Byrne, and K.T. Vaughan. 2002. A role for regulated binding of p150Glued to microtubule plus ends in organelle transport. J. Cell Biol. 158:305–319
Wen, Y., C.H. Eng, J. Schmoranzer, N. Cabrera-Poch, E.J. Morris, M. Chen, B.J. Wallar, A.S. Alberts, and G.G. Gundersen. 2004. EB1 and APC bind to mDia to stabilize microtubules downstream of Rho and promote cell migration. Nat. Cell Biol. 6:820–830.
Wu, X., G.L. Tsan, and J.A. Hammer. 2005. Melanophillin and myosin Va track the microtubule plus end on EB1. J. Cell Biol. 171:201–207.
Wu, X.S., K. Rao, H. Zhang, F. Wang, J.R. Sellers, L.E. Matesic, N.G. Copeland, N.A. Jenkins, and J.A. Hammer III. 2002. Identification of an organelle receptor for myosin-Va. Nat. Cell Biol. 4:271–278.
Xiang, X., G. Han, D.A. Winkelmann, W. Zuo, and N.R. Morris. 2000. Dynamics of cytoplasmic dynein in living cells and the effect of a mutation in the dynactin complex actin-related protein Arp1. Curr. Biol. 10:603–606.(Kevin T. Vaughan)