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在缺乏PUF-8的情况下,GLD-2和GLD-1对生殖系分化和去分化的剂量依赖性效应。

Dose-Dependent Effects of GLD-2 and GLD-1 on Germline Differentiation and Dedifferentiation in the Absence of PUF-8.

作者信息

Park Youngyong, O'Rourke Samuel, Taki Faten A, Alfhili Mohammad A, Lee Myon Hee

机构信息

Department of Internal Medicine, Division of Hematology/Oncology, Brody School of Medicine at East Carolina University, Greenville, NC, United States.

Department of Pharmacology, Weill Cornell Medical College, New York, NY, United States.

出版信息

Front Cell Dev Biol. 2020 Jan 24;8:5. doi: 10.3389/fcell.2020.00005. eCollection 2020.

Abstract

PUMILIO/FBF (PUF) proteins have a conserved function in stem cell regulation. PUF-8 protein inhibits the translation of target mRNAs by interacting with PUF binding element (PBE) in the 3' untranslated region (3' UTR). In this work, an analysis has identified [a poly(A) polymerase] as a putative PUF-8 target. Biochemical and reporter analyses showed that PUF-8 specifically binds to a PBE in 3' UTR and represses a GFP reporter gene carrying 3' UTR in the mitotic germ cells. GLD-2 enhances meiotic entry at least in part by activating GLD-1 (a KH motif-containing RNA-binding protein). Our genetic analyses also demonstrated that heterozygous genes in the absence of PUF-8 are competent for meiotic entry (early differentiation), but haplo-insufficient for the meiotic division (terminal differentiation) of spermatocytes. Indeed, the arrested spermatocytes return to mitotic cells via dedifferentiation, which results in germline tumors. Since these regulators are broadly conserved, we thus suggest that similar molecular mechanisms may control differentiation, dedifferentiation, and tumorigenesis in other organisms, including humans.

摘要

PUMILIO/FBF(PUF)蛋白在干细胞调控中具有保守功能。PUF-8蛋白通过与3'非翻译区(3'UTR)中的PUF结合元件(PBE)相互作用来抑制靶mRNA的翻译。在这项工作中,一项分析已鉴定出[一种聚腺苷酸聚合酶]作为推定的PUF-8靶标。生化分析和报告基因分析表明,PUF-8特异性结合3'UTR中的PBE,并在有丝分裂生殖细胞中抑制携带3'UTR的GFP报告基因。GLD-2至少部分地通过激活GLD-1(一种含KH基序的RNA结合蛋白)来促进减数分裂进入。我们的遗传学分析还表明,在没有PUF-8的情况下,杂合基因能够进行减数分裂进入(早期分化),但对精母细胞的减数分裂(终末分化)单倍体不足。实际上,停滞的精母细胞通过去分化回到有丝分裂细胞,这导致生殖系肿瘤。由于这些调节因子具有广泛的保守性,因此我们认为类似的分子机制可能控制包括人类在内的其他生物体中的分化、去分化和肿瘤发生。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7431/6992537/5d7fa422e2d5/fcell-08-00005-g004.jpg

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