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RBM46 对于配子发生是必不可少的,并在影响减数分裂黏连蛋白亚基的转录后作用中发挥功能。

RBM46 is essential for gametogenesis and functions in post-transcriptional roles affecting meiotic cohesin subunits.

机构信息

Shandong Key Laboratory of Reproductive Medicine, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan 250012, China.

Center for Reproductive Medicine, Shandong University, Jinan 250012, China.

出版信息

Protein Cell. 2022 Sep 14;14(1):51-63. doi: 10.1093/procel/pwac040. eCollection 2023 Jan.

Abstract

RBM46 is a germ cell-specific RNA-binding protein required for gametogenesis, but the targets and molecular functions of RBM46 remain unknown. Here, we demonstrate that RBM46 binds at specific motifs in the 3'UTRs of mRNAs encoding multiple meiotic cohesin subunits and show that RBM46 is required for normal synaptonemal complex formation during meiosis initiation. Using a recently reported, high-resolution technique known as LACE-seq and working with low-input cells, we profiled the targets of RBM46 at single-nucleotide resolution in leptotene and zygotene stage gametes. We found that RBM46 preferentially binds target mRNAs containing GCCUAU/GUUCGA motifs in their 3'UTRs regions. In knockout mice, the RBM46-target cohesin subunits displayed unaltered mRNA levels but had reduced translation, resulting in the failed assembly of axial elements, synapsis disruption, and meiotic arrest. Our study thus provides mechanistic insights into the molecular functions of RBM46 in gametogenesis and illustrates the power of LACE-seq for investigations of RNA-binding protein functions when working with low-abundance input materials.

摘要

RBM46 是一种生殖细胞特异性 RNA 结合蛋白,对于配子发生是必需的,但 RBM46 的靶标和分子功能仍然未知。在这里,我们证明 RBM46 结合在编码多个减数分裂黏合蛋白亚基的 mRNAs 的 3'UTR 中的特定基序上,并表明 RBM46 对于减数分裂起始过程中的正常联会复合体形成是必需的。使用最近报道的一种称为 LACE-seq 的高分辨率技术,并使用低输入细胞,我们在细线期和粗线期配子中以单核苷酸分辨率对 RBM46 的靶标进行了分析。我们发现 RBM46 优先结合其 3'UTR 区域中含有 GCCUAU/GUUCGA 基序的靶标 mRNAs。在 RBM46 敲除小鼠中,RBM46 靶标黏合蛋白亚基的 mRNA 水平没有改变,但翻译减少,导致轴丝元件的组装失败、联会破坏和减数分裂停滞。因此,我们的研究为 RBM46 在配子发生中的分子功能提供了机制见解,并说明了 LACE-seq 在使用低丰度输入材料研究 RNA 结合蛋白功能时的强大功能。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8e4f/9871953/2024c40168c8/pwac040_fig1.jpg

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