Regulation of meiotic recombination and prophase I progression in mammals

被引:90
作者
Cohen, PE
Pollard, JW
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
[2] Yeshiva Univ Albert Einstein Coll Med, Dept Obstet Gynecol & Womens Hlth, Ctr Studies Reprod Biol, Bronx, NY 10461 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Dev & Mol Biol, Bronx, NY 10461 USA
关键词
D O I
10.1002/bies.1145
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Meiosis is the process by which diploid germ cells divide to produce haploid gametes for sexual reproduction. The process is highly conserved in eukaryotes, however the recent availability of mouse models for meiotic recombination has revealed surprising regulatory differences between simple unicellular organisms and those with increasingly complex genomes. Moreover, in these higher eukaryotes, the intervention of physiological and sex-specific factors may also influence how meiotic recombination and progression are monitored and regulated. This review will focus on the recent studies involving mouse mutants for meiosis, and will highlight important differences between traditional model systems for meiosis (such as yeast) and those involving more complex cellular, physiological and genetic criteria. BioEssays 23:996-1009, 2001. (C) 2001 John Wiley & Sons, Inc.
引用
收藏
页码:996 / 1009
页数:14
相关论文
共 81 条
[21]   Bureaucrats, state banks, and the efficiency of credit allocation: The experience of Chinese state-owned enterprises [J].
Cull, R ;
Xu, LC .
JOURNAL OF COMPARATIVE ECONOMICS, 2000, 28 (01) :1-31
[22]   Mouse MutS-like protein Msh5 is required for proper chromosome synapsis in male and female meiosis [J].
de Vries, SS ;
Baart, EB ;
Dekker, M ;
Siezen, A ;
de Rooij, DG ;
de Boer, P ;
te Riele, H .
GENES & DEVELOPMENT, 1999, 13 (05) :523-531
[23]  
Dolganov GM, 1996, MOL CELL BIOL, V16, P4832
[24]   The Nijmegen breakage syndrome protein is essential for Mre11 phosphorylation upon DNA damage [J].
Dong, ZW ;
Zhong, Q ;
Chen, PL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (28) :19513-19516
[25]   Mammalian MutS homologue 5 is required for chromosome pairing in meiosis [J].
Edelmann, W ;
Cohen, PE ;
Kneitz, B ;
Winand, N ;
Lia, M ;
Heyer, J ;
Kolodner, R ;
Pollard, JW ;
Kucherlapati, R .
NATURE GENETICS, 1999, 21 (01) :123-127
[26]   Meiotic pachytene arrest in MLH1-deficient mice [J].
Edelmann, W ;
Cohen, PE ;
Kane, M ;
Lau, K ;
Morrow, B ;
Bennett, S ;
Umar, A ;
Kunkel, T ;
Cattoretti, G ;
Chaganti, R ;
Pollard, JW ;
Kolodner, RD ;
Kucherlapati, R .
CELL, 1996, 85 (07) :1125-1134
[27]   THE BLOOMS-SYNDROME GENE-PRODUCT IS HOMOLOGOUS TO RECQ HELICASES [J].
ELLIS, NA ;
GRODEN, J ;
YE, TZ ;
STRAUGHEN, J ;
LENNON, DJ ;
CIOCCI, S ;
PROYTCHEVA, M ;
GERMAN, J .
CELL, 1995, 83 (04) :655-666
[28]   Human and mouse homologs of Schizosaccharomyces pombe rad1+ and Saccharomyces cerevisiae RAD17:: linkage to checkpoint control and mammalian meiosis [J].
Freire, R ;
Murguía, JR ;
Tarsounas, M ;
Lowndes, NF ;
Moens, PB ;
Jackson, SP .
GENES & DEVELOPMENT, 1998, 12 (16) :2560-2573
[29]   BLOOM-SYNDROME - A MENDELIAN PROTOTYPE OF SOMATIC MUTATIONAL DISEASE [J].
GERMAN, J .
MEDICINE, 1993, 72 (06) :393-406
[30]   The Werner syndrome protein is a DNA helicase [J].
Gray, MD ;
Shen, JC ;
KamathLoeb, AS ;
Blank, A ;
Sopher, BL ;
Martin, GM ;
Oshima, J ;
Loeb, LA .
NATURE GENETICS, 1997, 17 (01) :100-103