Controls of germline stem cells, entry into meiosis, and the Sperm/Oocyte decision in Caenorhabditis elegans

被引:283
作者
Kimble, Judith [1 ]
Crittenden, Sarah L. [1 ]
机构
[1] Univ Wisconsin, Howard Hughes Med Inst, Dept Biochem, Madison, WI 53706 USA
关键词
stem cell niche; mitosis/meiosis decision; Notch signaling; PUF proteins; CPEB; regulatory network; cell number; hermaphrodite evolution;
D O I
10.1146/annurev.cellbio.23.090506.123326
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The Caenorhabditis elegans germ line provides an exceptional model for analysis of the molecular controls governing stem cell maintenance, the cell cycle transition from mitosis to meiosis, and the choice of sexual identity-sperm or oocyte. Germline stem cells are maintained in an undifferentiated state within a well-defined niche formed by a single somatic cell, the distal tip cell (DTC). In both sexes, the DTC employs GLP-1/Notch signaling and FBF/PUF RNA-binding proteins to maintain stein cells and promote mitotic divisions, three additional RNA regulators (GLD-1/quaking, GLD-2/poly(A) polymerase, and GLD-3/Bicaudal-C) control entry into meiosis, and FOG-1/CPEB and FOG-3/Tob proteins govern sperm specification. These key regulators are part of a robust regulatory network that controls germ cell proliferation, stem cell maintenance, and sex determination. Parallels with controls in other organisms include the use of PUF proteins for stem cell maintenance and the prominence of mRNA regulation for the control of germline development.
引用
收藏
页码:405 / 433
页数:29
相关论文
共 126 条
[91]   Reciprocal asymmetry of SYS-1/β-catenin and POP-1/TCF controls asymmetric divisions in Caenorhabditis elegans [J].
Phillips, Bryan T. ;
Kidd, Ambrose R., III ;
King, Ryan ;
Hardin, Jeff ;
Kimble, Judith .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2007, 104 (09) :3231-3236
[92]  
Puoti A, 1999, MOL CELL BIOL, V19, P2189
[93]   The hermaphrodite sperm/oocyte switch requires the Caenorhabditis elegans homologs of PRP2 and PRP22 [J].
Puoti, A ;
Kimble, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2000, 97 (07) :3276-3281
[94]   A role for Wnt signalling in self-renewal of haematopoietic stem cells [J].
Reya, T ;
Duncan, AW ;
Ailles, L ;
Domen, J ;
Scherer, DC ;
Willert, K ;
Hintz, L ;
Nusse, R ;
Weissman, IL .
NATURE, 2003, 423 (6938) :409-414
[95]   Wnt signalling in stem cells and cancer [J].
Reya, T ;
Clevers, H .
NATURE, 2005, 434 (7035) :843-850
[96]   Interaction of BTG1 and p53-regulated BTG2 gene products with mCaf1, the murine homolog of a component of the yeast CCR4 transcriptional regulatory complex [J].
Rouault, JP ;
Prévôt, D ;
Berthet, C ;
Birot, AM ;
Billaud, M ;
Magaud, JP ;
Corbo, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (35) :22563-22569
[97]   RNA target specificity of the STAR/GSG domain post-transcriptional regulatory protein GLD-1 [J].
Ryder, SP ;
Frater, LA ;
Abramovitz, DL ;
Goodwin, EB ;
Williamson, JR .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (01) :20-28
[98]  
SCHEDL T, 1988, GENETICS, V119, P43
[99]   RNA-regulated TRA-1 nuclear export controls sexual fate [J].
Segal, SP ;
Graves, LE ;
Verheyden, J ;
Goodwin, EB .
DEVELOPMENTAL CELL, 2001, 1 (04) :539-551
[100]   The sys-1 and sys-3 genes cooperate with Wnt signaling to establish the proximal-distal axis of the Caenorhabditis elegans gonad [J].
Siegfried, KR ;
Kidd, AR ;
Chesney, MA ;
Kimble, J .
GENETICS, 2004, 166 (01) :171-186