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一种含RNA识别基序的蛋白质在未配对DNA介导的减数分裂沉默中发挥作用。

An RNA Recognition Motif-Containing Protein Functions in Meiotic Silencing by Unpaired DNA.

作者信息

Samarajeewa Dilini A, Manitchotpisit Pennapa, Henderson Miranda, Xiao Hua, Rehard David G, Edwards Kevin A, Shiu Patrick K T, Hammond Thomas M

机构信息

School of Biological Sciences, Illinois State University, Normal, Illinois 61790.

Division of Biological Sciences, University of Missouri, Columbia, Missouri 65211.

出版信息

G3 (Bethesda). 2017 Aug 7;7(8):2871-2882. doi: 10.1534/g3.117.041848.

Abstract

Meiotic silencing by unpaired DNA (MSUD) is a biological process that searches pairs of homologous chromosomes (homologs) for segments of DNA that are unpaired. Genes found within unpaired segments are silenced for the duration of meiosis. In this report, we describe the identification and characterization of , a gene that encodes a protein with an RNA recognition motif (RRM). Orthologs of are found in a wide range of ascomycete fungi. In , is required for a fully efficient MSUD response to unpaired genes. Additionally, at least one parent must have a functional allele for a cross to produce ascospores. Although -null crosses are barren, strains grow at a wild-type (wt) rate and appear normal under vegetative growth conditions. With respect to expression, is transcribed at baseline levels in early vegetative cultures, at slightly higher levels in mating-competent cultures, and is at its highest level during mating. These findings suggest that SAD-7 is specific to mating-competent and sexual cultures. Although the role of SAD-7 in MSUD remains elusive, green fluorescent protein (GFP)-based tagging studies place SAD-7 within nuclei, perinuclear regions, and cytoplasmic foci of meiotic cells. This localization pattern is unique among known MSUD proteins and raises the possibility that SAD-7 coordinates nuclear, perinuclear, and cytoplasmic aspects of MSUD.

摘要

未配对DNA介导的减数分裂沉默(MSUD)是一种生物学过程,该过程会在成对的同源染色体(同源物)中搜寻未配对的DNA片段。在减数分裂期间,位于未配对片段中的基因会被沉默。在本报告中,我们描述了一个基因的鉴定和特征,该基因编码一种带有RNA识别基序(RRM)的蛋白质。在多种子囊菌中都发现了该基因的直系同源物。在某物种中,对于未配对基因产生完全有效的MSUD反应而言,该基因是必需的。此外,至少有一个亲本必须具有功能性的该基因等位基因,杂交才能产生子囊孢子。尽管该基因缺失的杂交组合不育,但该基因缺失的菌株以野生型(wt)速率生长,并且在营养生长条件下看起来正常。就表达而言,该基因在早期营养培养物中以基础水平转录,在具备交配能力的培养物中略高,而在交配期间处于最高水平。这些发现表明SAD - 7特定于具备交配能力的有性培养物。尽管SAD - 7在MSUD中的作用仍然难以捉摸,但基于绿色荧光蛋白(GFP)的标记研究将SAD - 7定位在减数分裂细胞的细胞核、核周区域和细胞质灶中。这种定位模式在已知的MSUD蛋白中是独特的,并增加了SAD - 7协调MSUD的核、核周和细胞质方面的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9cbe/5555490/57176c5851ce/2871f1.jpg

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