ILP1 和 NTR1 在拟南芥剪接体复合物解体过程中影响 U6 snRNA 的稳定性。

IF 4.2 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Jiaming Wu , Wei Chen , Shengchao Ge , Xueliang Liu , Junling Shan , Meishan Zhang , Yuan Su , Yunfeng Liu
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引用次数: 0

摘要

U6 snRNA是富含尿苷的非编码RNA之一,在各种细胞中含量丰富且稳定,是内含子-片段剪接体(ILS)复合物的核心颗粒。多倍体1-1D(ILP1)和NTC相关蛋白1(NTR1)是ILS复合物的两个保守的解体因子,它们能在完成内含子剪接后促进ILS复合物的解体。ILP1 和 NTR1 的功能受损会导致 U6 水平升高,而组成 ILS 复合物的其他 snRNA 则不受影响。我们发现 ILP1 和 NTR1 对 U6 snRNA 的转录、3'端磷酸结构或寡聚(U)尾没有影响。此外,我们还发现 ILP1 和 NTR1 的突变会导致 ILS 复合物的积累,阻碍 U6 与剪接因子的分离,导致 U6 的半衰期延长,最终引起 U6 snRNA 水平的升高。我们的发现拓宽了对ILS分解因子ILP1和NTR1功能的理解,并为U6和ILS之间的动态分解提供了见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
ILP1 and NTR1 affect the stability of U6 snRNA during spliceosome complex disassembly in Arabidopsis

U6 snRNA is one of the uridine-rich non-coding RNAs, abundant and stable in various cells, function as core particles in the intron-lariat spliceosome (ILS) complex. The Increased Level of Polyploidy1–1D (ILP1) and NTC-related protein 1 (NTR1), two conserved disassembly factors of the ILS complex, facilitates the disintegration of the ILS complex after completing intron splicing. The functional impairment of ILP1 and NTR1 lead to increased U6 levels, while other snRNAs comprising the ILS complex remained unaffected. We revealed that ILP1 and NTR1 had no impact on the transcription, 3’ end phosphate structure or oligo(U) tail of U6 snRNA. Moreover, we uncovered that the mutation of ILP1 and NTR1 resulted in the accumulation of ILS complexes, impeding the dissociation of U6 from splicing factors, leading to an extended half-life of U6 and ultimately causing an elevation in U6 snRNA levels. Our findings broaden the understanding of the functions of ILS disassembly factors ILP1 and NTR1, and providing insights into the dynamic disassembly between U6 and ILS.

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来源期刊
Plant Science
Plant Science 生物-生化与分子生物学
CiteScore
9.10
自引率
1.90%
发文量
322
审稿时长
33 days
期刊介绍: Plant Science will publish in the minimum of time, research manuscripts as well as commissioned reviews and commentaries recommended by its referees in all areas of experimental plant biology with emphasis in the broad areas of genomics, proteomics, biochemistry (including enzymology), physiology, cell biology, development, genetics, functional plant breeding, systems biology and the interaction of plants with the environment. Manuscripts for full consideration should be written concisely and essentially as a final report. The main criterion for publication is that the manuscript must contain original and significant insights that lead to a better understanding of fundamental plant biology. Papers centering on plant cell culture should be of interest to a wide audience and methods employed result in a substantial improvement over existing established techniques and approaches. Methods papers are welcome only when the technique(s) described is novel or provides a major advancement of established protocols.
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