Nuclear reorganization and homologous chromosome pairing during meiotic prophase require C-elegans chk-2

被引:176
作者
MacQueen, AJ [1 ]
Villeneuve, AM [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
关键词
meiosis; chromosome pairing; checkpoint; C; elegans; Chk2; chk-2;
D O I
10.1101/gad.902601
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Analysis of mutants defective in meiotic chromosome pairing has uncovered a role for Caenorhabditis: elegans chk-2 in initial establishment of pairing between homologous chromosomes during early meiotic prophase. chk-e is also required for the major spatial reorganization of nuclei that normally accompanies the onset of pairing, suggesting a mechanistic coupling of these two events. Despite failures in pairing, nuclear reorganization, and crossover recombination, chk-e mutants undergo many other aspects of meiotic chromosome morphogenesis and complete gametogenesis. Although chk-2 encodes a C. elegans ortholog of the Cds1/Chk2 checkpoint protein kinases, germ-line nuclei in chk-2 mutants are competent to arrest proliferation in response to replication inhibition and to trigger DNA damage checkpoint responses to ionizing radiation. However, chk-2 mutants are defective in triggering the pachytene DNA damage checkpoint in response to an intermediate block in the meiotic recombination pathway, suggesting that chk-2 is required either for initiation of meiotic recombination or for monitoring a specific subset of DNA damage lesions. Wt propose that chk-e functions during premeiotic S phase to enable chromosomes to become competent for subsequent meiotic prophase events and/or to coordinate replication with entry into prophase.
引用
收藏
页码:1674 / 1687
页数:14
相关论文
共 60 条
[1]  
Albertson DG, 1997, C ELEGANS, P47
[2]  
[Anonymous], 1997, C ELEGANS
[3]   IDENTIFICATION AND CHARACTERIZATION OF A YEAST NUCLEOLAR PROTEIN THAT IS SIMILAR TO A RAT-LIVER NUCLEOLAR PROTEIN [J].
ARIS, JP ;
BLOBEL, G .
JOURNAL OF CELL BIOLOGY, 1988, 107 (01) :17-31
[4]   Pachytene exit controlled by reversal of Mek1-dependent phosphorylation [J].
Bailis, JM ;
Roeder, GS .
CELL, 2000, 101 (02) :211-221
[5]   Synaptonemal complex morphogenesis and sister-chromatid cohesion require Mek1-dependent phosphorylation of a meiotic chromosomal protein [J].
Bailis, JM ;
Roeder, GS .
GENES & DEVELOPMENT, 1998, 12 (22) :3551-3563
[6]   Telomeres cluster de novo before the initiation of synapsis: A three-dimensional spatial analysis of telomere positions before and during meiotic prophase [J].
Bass, HW ;
Marshall, WF ;
Sedat, JW ;
Agard, DA ;
Cande, WZ .
JOURNAL OF CELL BIOLOGY, 1997, 137 (01) :5-18
[7]   Direct coupling between meiotic DNA replication and recombination initiation [J].
Borde, V ;
Goldman, ASH ;
Lichten, M .
SCIENCE, 2000, 290 (5492) :806-809
[8]  
Cha RS, 2000, GENE DEV, V14, P493
[9]   Mammalian Chk2 is a downstream effector of the ATM-dependent DNA damage checkpoint pathway [J].
Chaturvedi, P ;
Eng, WK ;
Zhu, Y ;
Mattern, MR ;
Mishra, R ;
Hurle, MR ;
Zhang, XL ;
Annan, RS ;
Lu, Q ;
Faucette, LF ;
Scott, GF ;
Li, XT ;
Carr, SA ;
Johnson, RK ;
Winkler, JD ;
Zhou, BBS .
ONCOGENE, 1999, 18 (28) :4047-4054
[10]   IVE (Image Visualization Environment): A software platform for all three-dimensional microscopy applications [J].
Chen, H ;
Hughes, DD ;
Chan, TA ;
Sedat, JW ;
Agard, DA .
JOURNAL OF STRUCTURAL BIOLOGY, 1996, 116 (01) :56-60