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Mechanisms of translational regulation in synaptic plasticity.突触可塑性中的翻译调控机制。
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Genome-wide analysis of mRNA targets for Caenorhabditis elegans FBF, a conserved stem cell regulator.全基因组分析 Caenorhabditis elegans FBF 的 mRNA 靶标,FBF 是一种保守的干细胞调节因子。
Proc Natl Acad Sci U S A. 2010 Feb 23;107(8):3936-41. doi: 10.1073/pnas.1000495107. Epub 2010 Feb 8.
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Antagonism between GLD-2 binding partners controls gamete sex.GLD-2结合伴侣之间的拮抗作用控制配子性别。
Dev Cell. 2009 May;16(5):723-33. doi: 10.1016/j.devcel.2009.04.002.
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Identification of genes expressed in the hermaphrodite germ line of C. elegans using SAGE.利用基因表达序列分析(SAGE)鉴定秀丽隐杆线虫雌雄同体生殖系中表达的基因。
BMC Genomics. 2009 May 9;10:213. doi: 10.1186/1471-2164-10-213.
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Two conserved regulatory cytoplasmic poly(A) polymerases, GLD-4 and GLD-2, regulate meiotic progression in C. elegans.两种保守的调节性细胞质聚腺苷酸聚合酶GLD-4和GLD-2调节秀丽隐杆线虫的减数分裂进程。
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Making synaptic plasticity and memory last: mechanisms of translational regulation.使突触可塑性和记忆持久:翻译调控机制
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10
PAP- and GLD-2-type poly(A) polymerases are required sequentially in cytoplasmic polyadenylation and oogenesis in Drosophila.PAP型和GLD-2型聚腺苷酸聚合酶在果蝇的细胞质聚腺苷酸化和卵子发生过程中依次发挥作用。
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GLD-2/RNP-8 细胞质多聚(A)聚合酶是卵发生程序的广谱调节剂。

GLD-2/RNP-8 cytoplasmic poly(A) polymerase is a broad-spectrum regulator of the oogenesis program.

机构信息

Department of Biochemistry and Howard Hughes Medical Institute, University of Wisconsin, Madison, WI 53706, USA.

出版信息

Proc Natl Acad Sci U S A. 2010 Oct 5;107(40):17445-50. doi: 10.1073/pnas.1012611107. Epub 2010 Sep 20.

DOI:10.1073/pnas.1012611107
PMID:20855596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2951458/
Abstract

Regulated polyadenylation is a broadly conserved mechanism that controls key events during oogenesis. Pivotal to that mechanism is GLD-2, a catalytic subunit of cytoplasmic poly(A) polymerase (PAP). Caenorhabditis elegans GLD-2 forms an active PAP with multiple RNA-binding partners to regulate diverse aspects of germline and early embryonic development. One GLD-2 partner, RNP-8, was previously shown to influence oocyte fate specification. Here we use a genomic approach to identify transcripts selectively associated with both GLD-2 and RNP-8. Among the 335 GLD-2/RNP-8 potential targets, most were annotated as germline mRNAs and many as maternal mRNAs. These targets include gld-2 and rnp-8 themselves, suggesting autoregulation. Removal of either GLD-2 or RNP-8 resulted in shortened poly(A) tails and lowered abundance of four target mRNAs (oma-2, egg-1, pup-2, and tra-2); GLD-2 depletion also lowered the abundance of most GLD-2/RNP-8 putative target mRNAs when assayed on microarrays. Therefore, GLD-2/RNP-8 appears to polyadenylate and stabilize its target mRNAs. We also provide evidence that rnp-8 influences oocyte development; rnp-8 null mutants have more germ cell corpses and fewer oocytes than normal. Furthermore, RNP-8 appears to work synergistically with another GLD-2-binding partner, GLD-3, to ensure normal oogenesis. We propose that the GLD-2/RNP-8 enzyme is a broad-spectrum regulator of the oogenesis program that acts within an RNA regulatory network to specify and produce fully functional oocytes.

摘要

调控的多聚腺苷酸化是一种广泛保守的机制,它控制着卵子发生过程中的关键事件。这一机制的关键是 GLD-2,细胞质多聚(A)聚合酶(PAP)的催化亚基。秀丽隐杆线虫 GLD-2 与多个 RNA 结合伙伴形成活性 PAP,调节生殖系和早期胚胎发育的多个方面。GLD-2 的一个伙伴 RNP-8 先前被证明影响卵母细胞命运的特化。在这里,我们使用基因组方法来鉴定与 GLD-2 和 RNP-8 都有选择性关联的转录本。在 335 个 GLD-2/RNP-8 潜在靶标中,大多数被注释为生殖系 mRNA,许多为母本 mRNA。这些靶标包括 gld-2 和 rnp-8 本身,表明存在自身调控。去除 GLD-2 或 RNP-8 都会导致 poly(A)尾巴缩短,以及四个靶标 mRNA(oma-2、egg-1、pup-2 和 tra-2)的丰度降低;当在微阵列上进行检测时,GLD-2 耗竭也降低了大多数 GLD-2/RNP-8 假定靶标 mRNA 的丰度。因此,GLD-2/RNP-8 似乎可以多聚腺苷酸化并稳定其靶标 mRNA。我们还提供了证据表明 rnp-8 影响卵母细胞的发育;rnp-8 缺失突变体比正常情况下有更多的生殖细胞尸体和更少的卵母细胞。此外,RNP-8 似乎与另一个与 GLD-2 结合的伙伴 GLD-3 协同作用,以确保正常的卵子发生。我们提出,GLD-2/RNP-8 酶是卵子发生程序的广谱调节剂,它在 RNA 调控网络内发挥作用,以指定和产生具有完全功能的卵母细胞。