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U6小核RNA m⁶A甲基转移酶Mtl16突变等位基因的分离及其与剪接突变体的遗传相互作用的表征 。

Isolation of mutant alleles of the U6 snRNA m A methyltransferase Mtl16 and characterization of their genetic interactions with splicing mutants in .

作者信息

Willet Alaina H, Ren Liping, Turner Lesley A, Gould Kathleen L

机构信息

Department of Cell and Developmental Biology, Vanderbilt University School of Medicine, Nashville, TN US.

出版信息

MicroPubl Biol. 2023 Aug 11;2023. doi: 10.17912/micropub.biology.000948. eCollection 2023.

Abstract

Dim1 is a conserved essential component of the U4/U6.U5 tri-snRNP complex essential for pre-mRNA splicing. In a synthetic lethal screen with the temperature-sensitive mutant, we isolated multiple alleles of non-essential that encodes the U6 snRNA m A methyltransferase. Further genetic analysis revealed strong and specific negative genetic interactions between and a mutation in the Dim1 binding partner, Prp31, and between and a mutation in the Prp31 binding partner, Prp6. Our work provides additional tools to study pre-mRNA splicing in and biological confirmation of the importance of the Prp6-Prp31-Dim1-U6 snRNA interactions for pre-mRNA splicing.

摘要

Dim1是U4/U6.U5三小核核糖核蛋白复合体中一个保守的必需成分,对前体mRNA剪接至关重要。在与温度敏感突变体的合成致死筛选中,我们分离出了编码U6 snRNA mA甲基转移酶的非必需基因的多个等位基因。进一步的遗传分析揭示了该基因与Dim1结合伴侣Prp31中的一个突变之间,以及该基因与Prp31结合伴侣Prp6中的一个突变之间存在强烈且特异性的负遗传相互作用。我们的工作为研究酿酒酵母中的前体mRNA剪接提供了额外的工具,并从生物学角度证实了Prp6-Prp31-Dim1-U6 snRNA相互作用对前体mRNA剪接的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a7ed/10457676/41152946bd07/25789430-2023-micropub.biology.000948.jpg

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