Cell Cycle
ISSN: 1538-4101 (Print) 1551-4005 (Online) Journal homepage: http://www.tandfonline.com/loi/kccy20
Mad1 at the Golgi apparatus: a story beyond kinetochores Jun Wan & Beth A Weaver To cite this article: Jun Wan & Beth A Weaver (2015) Mad1 at the Golgi apparatus: a story beyond kinetochores, Cell Cycle, 14:12, 1763-1764, DOI: 10.1080/15384101.2015.1032639 To link to this article: http://dx.doi.org/10.1080/15384101.2015.1032639
Accepted author version posted online: 27 May 2015.
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Date: 05 November 2015, At: 13:32
EDITORIALS: CELL CYCLE FEATURES Cell Cycle 14:12, 1763--1764; June 15, 2015; © 2015 Taylor & Francis Group, LLC
Mad1 at the Golgi apparatus: a story beyond kinetochores Jun Wan1 and Beth A Weaver2,* Physiology Training Program; University of Wisconsin, Madison, WI USA; 2Department of Cell and Regenerative Biology and Carbone Cancer Center; University of Wisconsin, Madison, WI USA
Downloaded by [75.83.6.73] at 13:32 05 November 2015
1
It is often overlooked that genes that play well-characterized, essential roles during one stage of the cell cycle may also perform completely unrelated, but still critical functions during other cell cycle stages. Alternate functions of well-studied proteins are often difficult to define because they are outside the area of expertise of laboratories that focus on pathways and processes in which the protein serves its canonical role. However, a full understanding of the roles a protein plays throughout the cell cycle is critical for accurate interpretation of loss of function and overexpression studies that occur over multiple cell cycles, particularly experiments in whole animals during development and aging. Mitotic arrest deficient 1 (Mad1) was first identified as one of the genes essential for the mitotic checkpoint (also known as the spindle assembly checkpoint), which prevents chromosome missegregation and aneuploidy by delaying anaphase onset until all chromosomes have made stable attachments to spindle microtubules. We have focused our attention on this protein because overexpression of Mad1 is common in tumors and is a marker of poor prognosis.1 The function of Mad1 during mitosis has been well studied and is largely dependent on its association with another mitotic checkpoint component, Mad2. Mad1 accumulates at kinetochores on unattached chromosomes that have not yet made stable attachments to spindle microtubules and would therefore be randomly segregated if the cells entered anaphase. At unattached kinetochores, Mad1 recruits and converts Mad2 from an
inactive, open form into an active, closed form that inhibits the Anaphase Promoting Complex/Cyclosome (APC/C) bound to its specificity factor Cdc20.2 Although the function of Mad1 in mitosis has been well studied, Mad1 is expressed throughout the cell cycle and its protein levels do not exhibit cell cycle regulation.1 Previous evidence indicated that Mad1 interacts with Mad2 throughout the cell cycle.2 In interphase, both Mad1 and Mad2 are associated with the nuclear pore complex. Nuclear pore binding stabilizes both proteins and helps to scaffold production of APC/C-Cdc20 inhibitors during interphase, which delays activation of APC/C-Cdc20 in mitosis.3 It remains unclear whether nuclear pore-associated pools of Mad1 and Mad2 perform functional roles during interphase in vertebrates. Recently we identified an unsuspected Golgi-localized pool of Mad1 (Fig. 1).4 Golgi localization of Mad1 was confirmed by immunofluorescence experiments and cell fractionation. The perinuclear Mad1 signal dispersed after treatment with the microtubule poison vinblastine or with an inhibitor of protein trafficking, Brefeldin A, both of which cause disassembly of the Golgi. Transient and stable depletion of Mad1 removed the Golgi localized pool. Interestingly, unlike kinetochore and nuclear pore bound pools of Mad1, Golgi associated Mad1 is independent of Mad2 (Fig. 1). To determine whether Mad1 functions in secretion at the Golgi, we generated several cell lines in which Mad1 expression was stably knocked down
(Mad1-KD cells). Previous studies have identified the proteins required for global secretion, which did not include Mad1.5 Consistent with this, we found that the depletion of Mad1 did not affect secretion of VSVG or EGFR. However, testing of a variety of additional secretory proteins revealed that Mad1 knockdown results in impaired secretion of a5 integrin. In complex with b1 integrin, a5 integrin serves as a key molecule on the plasma membrane to anchor cells to the extracellular matrix (ECM) component fibronectin. In Mad1-KD cells, the a5 integrin subunit was enriched in the Golgi and showed less accumulation at the cell surface than in wild type cells (Fig. 1). The defects in a5 integrin secretion suggested that Mad1-KD cells exhibit impaired cellular adhesion and migration on fibronectin. Consistent with this, fewer Mad1-KD cells adhered to and spread on fibronectin coated plates compared to wild type cells. Mad1-KD cells also exhibited impaired migration on fibronectin in cell culture wounding and transwell migration assays.4 These effects were not due to decreased proliferation, and were also apparent in single cell migration tracking assays. Overexpression of Mad1 enhanced migration on fibronectin, further supporting a role for Mad1 in secretion of a5 integrin. Notably, cells depleted of Mad2 did not show defects in secretion of a5 integrin or spreading on fibronectin.4 In the future, it will be important to gain a mechanistic understanding of Mad1 localization to the Golgi and its
*Correspondence to: Beth A Weaver; Email: [email protected] Submitted: 02/24/2015; Revised: 02/26/2015; Accepted: 02/27/2015 http://dx.doi.org/10.1080/15384101.2015.1032639 Comment on: Wan J, et al. A Golgi-localized pool of the mitotic checkpoint component Mad1 controls integrin secretion and cell migration. Curr Biol 2014; 24 (22):2687–92; PMID:25447996; http://dx.doi.org/10.1016/j.cub.2014.09.052
www.tandfonline.com
Cell Cycle
1763
Downloaded by [75.83.6.73] at 13:32 05 November 2015
Figure 1. Mad1 localizes to the Golgi where it regulates secretion of a5 integrin and cell migration. (Left) Unlike Mad1 localization to the nucleus and nuclear envelope, the localization of Mad1 on the Golgi is independent of Mad2. Golgi-associated Mad1 facilitates the secretion of a5-integrin, which along with its binding partner b1-integrin, forms the cell surface receptor for the extracellular matrix (ECM) protein fibronectin. (Right) Down-regulation of Mad1 causes accumulation of a5integrin in the Golgi and decreases cell surface localization of a5-integrin and migration on fibronectin.
regulation of integrin secretion. It will also be of interest to determine whether Mad1 upregulation, which frequently occurs in References 1. Ryan SD, et al. Proc Natl Acad Sci U S A 2012; 109: E2205–14; PMID:22778409; http://dx.doi.org/ 10.1073/pnas.1201911109 2. Chen RH, et al. Mol Biol Cell 1999; 10:2607–18; PMID:10436016; http://dx.doi.org/10.1091/mbc.10. 8.2607
1764
Since Mad1 plays a well-established role in the mitotic checkpoint, mouse models expressing altered levels of Mad1 (and multiple other mitotic checkpoint genes) have been used to assess the effects of chromosome missegregation and aneuploidy on tumorigenesis. Our data demonstrating a role for Mad1 in secretion and cellular motility highlight the fact that proteins that are present throughout the cell cycle have the potential to participate in additional functions that may influence tumor phenotype. With respect to aneuploidy, certain animals with mitotic checkpoint defects are tumor prone, others are not, and some actually exhibit fewer tumors than controls, depending on the specific genetic mutations involved.6,7 This highlights the more general caveat that unknown functions during other stages of the cell cycle may have a significant impact on phenotypic outcomes of targeted genetic manipulations.
human breast cancer, potentiates cellular migration and metastasis. 3. Rodriguez-Bravo V, et al. Cell 2014; 156:1017–31; PMID:24581499; http://dx.doi.org/10.1016/j.cell. 2014.01.010 4. Wan J, et al. Curr Biol 2014; 24:2687–92; PMID:25447996; http://dx.doi.org/10.1016/j.cub.2014.09.052 5. Simpson JC, et al. Nat Cell Biol 2012; 14:764–74; PMID:22660414; http://dx.doi.org/10.1038/ncb2510
Cell Cycle
6. Zasadil LM, et al. Semin Cell Dev Biol 2013; 24:370–9; PMID:23416057; http://dx.doi.org/10.1016/j.semcdb. 2013.02.001 7. Ricke RM, et al. Trends Genet 2008; 24:457–66; PMID:18675487; http://dx.doi.org/10.1016/j.tig. 2008.07.002
Volume 14 Issue 12
ISSN: 1538-4101 (Print) 1551-4005 (Online) Journal homepage: http://www.tandfonline.com/loi/kccy20
Mad1 at the Golgi apparatus: a story beyond kinetochores Jun Wan & Beth A Weaver To cite this article: Jun Wan & Beth A Weaver (2015) Mad1 at the Golgi apparatus: a story beyond kinetochores, Cell Cycle, 14:12, 1763-1764, DOI: 10.1080/15384101.2015.1032639 To link to this article: http://dx.doi.org/10.1080/15384101.2015.1032639
Accepted author version posted online: 27 May 2015.
Submit your article to this journal
Article views: 208
View related articles
View Crossmark data
Full Terms & Conditions of access and use can be found at http://www.tandfonline.com/action/journalInformation?journalCode=kccy20 Download by: [75.83.6.73]
Date: 05 November 2015, At: 13:32
EDITORIALS: CELL CYCLE FEATURES Cell Cycle 14:12, 1763--1764; June 15, 2015; © 2015 Taylor & Francis Group, LLC
Mad1 at the Golgi apparatus: a story beyond kinetochores Jun Wan1 and Beth A Weaver2,* Physiology Training Program; University of Wisconsin, Madison, WI USA; 2Department of Cell and Regenerative Biology and Carbone Cancer Center; University of Wisconsin, Madison, WI USA
Downloaded by [75.83.6.73] at 13:32 05 November 2015
1
It is often overlooked that genes that play well-characterized, essential roles during one stage of the cell cycle may also perform completely unrelated, but still critical functions during other cell cycle stages. Alternate functions of well-studied proteins are often difficult to define because they are outside the area of expertise of laboratories that focus on pathways and processes in which the protein serves its canonical role. However, a full understanding of the roles a protein plays throughout the cell cycle is critical for accurate interpretation of loss of function and overexpression studies that occur over multiple cell cycles, particularly experiments in whole animals during development and aging. Mitotic arrest deficient 1 (Mad1) was first identified as one of the genes essential for the mitotic checkpoint (also known as the spindle assembly checkpoint), which prevents chromosome missegregation and aneuploidy by delaying anaphase onset until all chromosomes have made stable attachments to spindle microtubules. We have focused our attention on this protein because overexpression of Mad1 is common in tumors and is a marker of poor prognosis.1 The function of Mad1 during mitosis has been well studied and is largely dependent on its association with another mitotic checkpoint component, Mad2. Mad1 accumulates at kinetochores on unattached chromosomes that have not yet made stable attachments to spindle microtubules and would therefore be randomly segregated if the cells entered anaphase. At unattached kinetochores, Mad1 recruits and converts Mad2 from an
inactive, open form into an active, closed form that inhibits the Anaphase Promoting Complex/Cyclosome (APC/C) bound to its specificity factor Cdc20.2 Although the function of Mad1 in mitosis has been well studied, Mad1 is expressed throughout the cell cycle and its protein levels do not exhibit cell cycle regulation.1 Previous evidence indicated that Mad1 interacts with Mad2 throughout the cell cycle.2 In interphase, both Mad1 and Mad2 are associated with the nuclear pore complex. Nuclear pore binding stabilizes both proteins and helps to scaffold production of APC/C-Cdc20 inhibitors during interphase, which delays activation of APC/C-Cdc20 in mitosis.3 It remains unclear whether nuclear pore-associated pools of Mad1 and Mad2 perform functional roles during interphase in vertebrates. Recently we identified an unsuspected Golgi-localized pool of Mad1 (Fig. 1).4 Golgi localization of Mad1 was confirmed by immunofluorescence experiments and cell fractionation. The perinuclear Mad1 signal dispersed after treatment with the microtubule poison vinblastine or with an inhibitor of protein trafficking, Brefeldin A, both of which cause disassembly of the Golgi. Transient and stable depletion of Mad1 removed the Golgi localized pool. Interestingly, unlike kinetochore and nuclear pore bound pools of Mad1, Golgi associated Mad1 is independent of Mad2 (Fig. 1). To determine whether Mad1 functions in secretion at the Golgi, we generated several cell lines in which Mad1 expression was stably knocked down
(Mad1-KD cells). Previous studies have identified the proteins required for global secretion, which did not include Mad1.5 Consistent with this, we found that the depletion of Mad1 did not affect secretion of VSVG or EGFR. However, testing of a variety of additional secretory proteins revealed that Mad1 knockdown results in impaired secretion of a5 integrin. In complex with b1 integrin, a5 integrin serves as a key molecule on the plasma membrane to anchor cells to the extracellular matrix (ECM) component fibronectin. In Mad1-KD cells, the a5 integrin subunit was enriched in the Golgi and showed less accumulation at the cell surface than in wild type cells (Fig. 1). The defects in a5 integrin secretion suggested that Mad1-KD cells exhibit impaired cellular adhesion and migration on fibronectin. Consistent with this, fewer Mad1-KD cells adhered to and spread on fibronectin coated plates compared to wild type cells. Mad1-KD cells also exhibited impaired migration on fibronectin in cell culture wounding and transwell migration assays.4 These effects were not due to decreased proliferation, and were also apparent in single cell migration tracking assays. Overexpression of Mad1 enhanced migration on fibronectin, further supporting a role for Mad1 in secretion of a5 integrin. Notably, cells depleted of Mad2 did not show defects in secretion of a5 integrin or spreading on fibronectin.4 In the future, it will be important to gain a mechanistic understanding of Mad1 localization to the Golgi and its
*Correspondence to: Beth A Weaver; Email: [email protected] Submitted: 02/24/2015; Revised: 02/26/2015; Accepted: 02/27/2015 http://dx.doi.org/10.1080/15384101.2015.1032639 Comment on: Wan J, et al. A Golgi-localized pool of the mitotic checkpoint component Mad1 controls integrin secretion and cell migration. Curr Biol 2014; 24 (22):2687–92; PMID:25447996; http://dx.doi.org/10.1016/j.cub.2014.09.052
www.tandfonline.com
Cell Cycle
1763
Downloaded by [75.83.6.73] at 13:32 05 November 2015
Figure 1. Mad1 localizes to the Golgi where it regulates secretion of a5 integrin and cell migration. (Left) Unlike Mad1 localization to the nucleus and nuclear envelope, the localization of Mad1 on the Golgi is independent of Mad2. Golgi-associated Mad1 facilitates the secretion of a5-integrin, which along with its binding partner b1-integrin, forms the cell surface receptor for the extracellular matrix (ECM) protein fibronectin. (Right) Down-regulation of Mad1 causes accumulation of a5integrin in the Golgi and decreases cell surface localization of a5-integrin and migration on fibronectin.
regulation of integrin secretion. It will also be of interest to determine whether Mad1 upregulation, which frequently occurs in References 1. Ryan SD, et al. Proc Natl Acad Sci U S A 2012; 109: E2205–14; PMID:22778409; http://dx.doi.org/ 10.1073/pnas.1201911109 2. Chen RH, et al. Mol Biol Cell 1999; 10:2607–18; PMID:10436016; http://dx.doi.org/10.1091/mbc.10. 8.2607
1764
Since Mad1 plays a well-established role in the mitotic checkpoint, mouse models expressing altered levels of Mad1 (and multiple other mitotic checkpoint genes) have been used to assess the effects of chromosome missegregation and aneuploidy on tumorigenesis. Our data demonstrating a role for Mad1 in secretion and cellular motility highlight the fact that proteins that are present throughout the cell cycle have the potential to participate in additional functions that may influence tumor phenotype. With respect to aneuploidy, certain animals with mitotic checkpoint defects are tumor prone, others are not, and some actually exhibit fewer tumors than controls, depending on the specific genetic mutations involved.6,7 This highlights the more general caveat that unknown functions during other stages of the cell cycle may have a significant impact on phenotypic outcomes of targeted genetic manipulations.
human breast cancer, potentiates cellular migration and metastasis. 3. Rodriguez-Bravo V, et al. Cell 2014; 156:1017–31; PMID:24581499; http://dx.doi.org/10.1016/j.cell. 2014.01.010 4. Wan J, et al. Curr Biol 2014; 24:2687–92; PMID:25447996; http://dx.doi.org/10.1016/j.cub.2014.09.052 5. Simpson JC, et al. Nat Cell Biol 2012; 14:764–74; PMID:22660414; http://dx.doi.org/10.1038/ncb2510
Cell Cycle
6. Zasadil LM, et al. Semin Cell Dev Biol 2013; 24:370–9; PMID:23416057; http://dx.doi.org/10.1016/j.semcdb. 2013.02.001 7. Ricke RM, et al. Trends Genet 2008; 24:457–66; PMID:18675487; http://dx.doi.org/10.1016/j.tig. 2008.07.002
Volume 14 Issue 12
