The Puf RNA-binding proteins FBF-1 and FBF-2 inhibit the expression of synaptonemal complex proteins in germline stem cells

被引:46
作者
Merritt, Christopher [1 ]
Seydoux, Geraldine [1 ]
机构
[1] Johns Hopkins Sch Med, Ctr Cell Dynam, Howard Hughes Med Inst, Dept Mol Biol & Genet, Baltimore, MD 21205 USA
来源
DEVELOPMENT | 2010年 / 137卷 / 11期
关键词
Germ cells; Meiosis; Post-transcriptional regulation; C; elegans; C-ELEGANS; MEIOTIC INITIATION; HOMOLOG ALIGNMENT; CHROMOSOME AXES; IN-VIVO; MEIOSIS; SYNAPSIS; DIFFERENTIATION; PROLIFERATION; COMPONENT;
D O I
10.1242/dev.050799
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
FBF-1 and FBF-2 (collectively FBF) are two nearly identical Puf-domain RNA-binding proteins that regulate the switch from mitosis to meiosis in the C. elegans germline. In germline stem cells, FBF prevents premature meiotic entry by inhibiting the expression of meiotic regulators, such as the RNA-binding protein GLD-1. Here, we demonstrate that FBF also directly inhibits the expression of structural components of meiotic chromosomes. HIM-3, HTP-1, HTP-2, SYP-2 and SYP-3 are components of the synaptonemal complex (SC) that forms between homologous chromosomes during meiotic prophase. In wild-type germlines, the five SC proteins are expressed shortly before meiotic entry. This pattern depends on FBF binding sites in the 3' UTRs of the SC mRNAs. In the absence of FBF or the FBF binding sites, SC proteins are expressed precociously in germline stem cells and their precursors. SC proteins aggregate and SC formation fails at meiotic entry. Precocious SC protein expression is observed even when meiotic entry is delayed in fbf mutants by reducing GLD-1. We propose that parallel regulation by FBF ensures that in wild-type gonads, meiotic entry is coordinated with just-in-time synthesis of synaptonemal proteins.
引用
收藏
页码:1787 / 1798
页数:12
相关论文
共 50 条
[1]   CONTROL OF THE SPERM-OOCYTE SWITCH IN CAENORHABDITIS-ELEGANS HERMAPHRODITES BY THE FEM-3 3' UNTRANSLATED REGION [J].
AHRINGER, J ;
KIMBLE, J .
NATURE, 1991, 349 (6307) :346-348
[2]  
Anderson EL, 2008, P NATL ACAD SCI USA, V105, P14976, DOI [10.1073/pnas.0807297105, 10.1038/s41598-019-45839-z]
[3]  
Bailey TL., 1994, Proc Int Conf Intel Syst Mol Biol, V2, P28
[4]   Binding specificity and mRNA targets of a C-elegans PUF protein, FBF-1 [J].
Bernstein, D ;
Hook, B ;
Hajarnavis, A ;
Opperman, L ;
Wickens, M .
RNA, 2005, 11 (04) :447-458
[5]   ZHP-3 Acts at Crossovers to Couple Meiotic Recombination with Synaptonemal Complex Disassembly and Bivalent Formation in C-elegans [J].
Bhalla, Needhi ;
Wynne, David J. ;
Jantsch, Verena ;
Dernburg, Abby F. .
PLOS GENETICS, 2008, 4 (10)
[6]  
BRENNER S, 1974, GENETICS, V77, P71
[7]   Scratching the niche that controls Caenorhabditis elegans germline stem cells [J].
Byrd, Dana T. ;
Kimble, Judith .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2009, 20 (09) :1107-1113
[8]   A conserved protein network controls assembly of the outer kinetochore and its ability to sustain tension [J].
Cheeseman, IM ;
Niessen, S ;
Anderson, S ;
Hyndman, F ;
Yates, JR ;
Oegema, K ;
Desai, A .
GENES & DEVELOPMENT, 2004, 18 (18) :2255-2268
[9]   The transcriptional program of sporulation in budding yeast [J].
Chu, S ;
DeRisi, J ;
Eisen, M ;
Mulholland, J ;
Botstein, D ;
Brown, PO ;
Herskowitz, I .
SCIENCE, 1998, 282 (5389) :699-705
[10]   Progression from a stem cell-like state to early differentiation in the C. elegans germ line [J].
Cinquin, Olivier ;
Crittenden, Sarah L. ;
Morgan, Dyan E. ;
Kimble, Judith .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (05) :2048-2053