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Title: Structure of an intermediate conformer of the spindle checkpoint protein Mad2

Journal Article · · Proceedings of the National Academy of Sciences of the United States of America
 [1];  [2];  [1];  [3];  [1]
  1. Univ. of Texas Southwestern Medical Center, Dallas, TX (United States). Dept. of Pharmacology
  2. Univ. of Texas Southwestern Medical Center, Dallas, TX (United States). Dept. of Biochemistry
  3. Univ. of Texas Southwestern Medical Center, Dallas, TX (United States). Dept. of Pharmacology. Howard Hughes Medical Inst.

The spindle checkpoint senses unattached kinetochores during prometaphase and inhibits the anaphase-promoting complex or cyclosome (APC/C), thus ensuring accurate chromosome segregation. The checkpoint protein mitotic arrest deficient 2 (Mad2) is an unusual protein with multiple folded states. Mad2 adopts the closed conformation (C-Mad2) in a Mad1–Mad2 core complex. In mitosis, kinetochore-bound Mad1–C-Mad2 recruits latent, open Mad2 (O-Mad2) from the cytosol and converts it to an intermediate conformer (I-Mad2), which can then bind and inhibit the APC/C activator cell division cycle 20 (Cdc20) as C-Mad2. In this paper, we report the crystal structure and NMR analysis of I-Mad2 bound to C-Mad2. Although I-Mad2 retains the O-Mad2 fold in crystal and in solution, its core structural elements undergo discernible rigid-body movements and more closely resemble C-Mad2. Residues exhibiting methyl chemical shift changes in I-Mad2 form a contiguous, interior network that connects its C-Mad2–binding site to the conformationally malleable C-terminal region. Mutations of residues at the I-Mad2–C-Mad2 interface hinder I-Mad2 formation and impede the structural transition of Mad2. Finally, our study provides insight into the conformational activation of Mad2 and establishes the basis of allosteric communication between two distal sites in Mad2.

Research Organization:
Univ. of Texas Southwestern Medical Center, Dallas, TX (United States)
Sponsoring Organization:
USDOE; National Inst. of Health (NIH) (United States); Welch Foundation (United States)
Grant/Contract Number:
AC02-06CH11357; S10RR026461-01; I-1441; GM107415
OSTI ID:
1239415
Journal Information:
Proceedings of the National Academy of Sciences of the United States of America, Vol. 112, Issue 36; ISSN 0027-8424
Publisher:
National Academy of Sciences, Washington, DC (United States)Copyright Statement
Country of Publication:
United States
Language:
ENGLISH
Citation Metrics:
Cited by: 25 works
Citation information provided by
Web of Science

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Regulation of the meiotic divisions of mammalian oocytes and eggs journal June 2018
PRC2 is high maintenance journal May 2019
A sequential multi-target Mps1 phosphorylation cascade promotes spindle checkpoint signaling journal January 2017
TRIP13 and APC15 drive mitotic exit by turnover of interphase- and unattached kinetochore-produced MCC journal October 2018
Mechanism for remodelling of the cell cycle checkpoint protein MAD2 by the ATPase TRIP13 journal July 2018
Lessons from making the Structural Classification of Proteins (SCOP) and their implications for protein structure modelling journal June 2016
Docking ofCDK1with antibiotic drugs revealed novel therapeutic value in breast ductal cancerin situ journal June 2017
Micromanaging checkpoint proteins journal February 2017
Peptide inhibitors of the anaphase promoting-complex that cause sensitivity to microtubule poison journal June 2018
Mechanistic insight into TRIP13-catalyzed Mad2 structural transition and spindle checkpoint silencing journal December 2017
Dissecting the mechanisms of cell division journal June 2019