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3' UTRs are the primary regulators of gene expression in the C. elegans germline.

机译:3'UTR是秀丽隐杆线虫种系中基因表达的主要调节子。

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摘要

How genes are regulated to produce the correct assortment of proteins for every cell type is a fundamental question in biology. For many genes, regulation begins at the DNA level with the use of promoter sequences to control transcription. Regulation can also occur after transcription using sequences in the 3' untranslated region (UTR) of the mRNA to affect mRNA stability and/or translation [1]. The C. elegans gonad is an excellent tissue to study gene regulation during development: In the adult, germ cells are arranged in order of differentiation, with undifferentiated progenitors at one end of the gonad, cells in meiotic prophase in the middle, and gametes at the other end [2]. Using a transgenic assay, we have compared the contribution of promoters and 3' UTRs to gene regulation during germline development. We find that for most genes tested, 3' UTRs are sufficient for regulation. With the exception of promoters activated during spermatogenesis, promoters are permissive for expression in all germ cell types (from progenitors to oocytes and sperm). In progenitors, 3' UTRs inhibit the production of meiotic and oocyte proteins by posttranscriptional mechanisms involving PUF- and KH-domain RNA-binding proteins. Our findings indicate that many genes rely primarily on 3' UTRs, not promoters, for regulation during germline development.
机译:如何调节基因以产生每种细胞类型正确的蛋白质分类是生物学中的一个基本问题。对于许多基因而言,调节是通过使用启动子序列控制转录在DNA级别开始的。转录后也可以使用mRNA的3'非翻译区(UTR)中的序列进行调节,以影响mRNA的稳定性和/或翻译[1]。秀丽隐杆线虫性腺是研究发育过程中基因调控的极佳组织:成年细胞中,生殖细胞按分化顺序排列,在性腺的一端有未分化的祖细胞,在中间的减数分裂前期有细胞,在配子处有配子。另一端[2]。使用转基因分析,我们比较了种系发育过程中启动子和3'UTR对基因调控的贡献。我们发现,对于大多数测试的基因,3'UTRs足以进行调节。除了在精子发生过程中被激活的启动子外,启动子可以在所有生殖细胞类型(从祖细胞到卵母细胞和精子)中表达。在祖细胞中,3'UTR通过涉及PUF和KH域RNA结合蛋白的转录后机制抑制减数分裂和卵母细胞蛋白的产生。我们的发现表明,许多基因在种系发育过程中主要依靠3'UTR(而不是启动子)进行调控。

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