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秀丽隐杆线虫生殖系中丝分裂/减数分裂决定的调控

Regulation of the mitosis/meiosis decision in the Caenorhabditis elegans germline.

作者信息

Crittenden Sarah L, Eckmann Christian R, Wang Liaoteng, Bernstein David S, Wickens Marvin, Kimble Judith

机构信息

Howard Hughes Medical Institute, Madison, WI 53706, USA.

出版信息

Philos Trans R Soc Lond B Biol Sci. 2003 Aug 29;358(1436):1359-62. doi: 10.1098/rstb.2003.1333.

Abstract

During the development of multicellular organisms, the processes of growth and differentiation are kept in balance to generate and maintain tissues and organs of the correct size, shape and cellular composition. We have investigated the molecular controls of growth and differentiation in the Caenorhabditis elegans germline. A single somatic cell, called the distal tip cell, promotes mitotic proliferation in the adjacent germline by GLP-1/Notch signalling. Within the germline, the decisions between mitosis and meiosis and between spermatogenesis and oogenesis are controlled by a group of conserved RNA regulators. FBF, a member of the PUF (for Pumilio and FBF) family of RNA-binding proteins, promotes mitosis by repressing gld-1 mRNA activity; the GLD-1, GLD-2, GLD-3 and NOS-3 proteins promote entry into meiosis by regulating mRNAs that remain unknown. The regulatory balance between opposing FBF and GLD activities is crucial for controlling the extent of germline proliferation. PUF proteins regulate germline stem cells in both Drosophila and C. elegans and are localized to germline stem cells of the mammalian testis. Therefore, this post-transcriptional regulatory switch may be an ancient mechanism for controlling maintenance of stem cells versus differentiation.

摘要

在多细胞生物的发育过程中,生长和分化过程保持平衡,以产生和维持具有正确大小、形状和细胞组成的组织和器官。我们研究了秀丽隐杆线虫生殖系中生长和分化的分子调控机制。一个称为远端末梢细胞的体细胞通过GLP-1/Notch信号通路促进相邻生殖系中的有丝分裂增殖。在生殖系内,有丝分裂和减数分裂之间以及精子发生和卵子发生之间的决定由一组保守的RNA调节因子控制。FBF是RNA结合蛋白PUF(Pumilio和FBF)家族的成员,通过抑制gld-1 mRNA活性促进有丝分裂;GLD-1、GLD-2、GLD-3和NOS-3蛋白通过调节未知的mRNA促进进入减数分裂。FBF和GLD活性之间的调节平衡对于控制生殖系增殖的程度至关重要。PUF蛋白在果蝇和秀丽隐杆线虫中都调节生殖系干细胞,并定位于哺乳动物睾丸的生殖系干细胞。因此,这种转录后调控开关可能是控制干细胞维持与分化的古老机制。

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