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SCR106 剪接因子通过维持水稻中的 RNA 剪接来调节非生物胁迫反应。

SCR106 splicing factor modulates abiotic stress responses by maintaining RNA splicing in rice.

机构信息

Laboratory for Genome Engineering and Synthetic Biology, Division of Biological Sciences, 4700 King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.

Laboratory of Plant Cell and Developmental Biology, Division of Biological Sciences, 4700 King Abdullah University of Science and Technology, Thuwal 23955-6900, Saudi Arabia.

出版信息

J Exp Bot. 2024 Feb 2;75(3):802-818. doi: 10.1093/jxb/erad433.

DOI:10.1093/jxb/erad433
PMID:37924151
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10837019/
Abstract

Plants employ sophisticated molecular machinery to fine-tune their responses to growth, developmental, and stress cues. Gene expression influences plant cellular responses through regulatory processes such as transcription and splicing. Pre-mRNA is alternatively spliced to increase the genome coding potential and further regulate expression. Serine/arginine-rich (SR) proteins, a family of pre-mRNA splicing factors, recognize splicing cis-elements and regulate both constitutive and alternative splicing. Several studies have reported SR protein genes in the rice genome, subdivided into six subfamilies based on their domain structures. Here, we identified a new splicing factor in rice with an RNA recognition motif (RRM) and SR-dipeptides, which is related to the SR proteins, subfamily SC. OsSCR106 regulates pre-mRNA splicing under abiotic stress conditions. It localizes to the nuclear speckles, a major site for pre-mRNA splicing in the cell. The loss-of-function scr106 mutant is hypersensitive to salt, abscisic acid, and low-temperature stress, and harbors a developmental abnormality indicated by the shorter length of the shoot and root. The hypersensitivity to stress phenotype was rescued by complementation using OsSCR106 fused behind its endogenous promoter. Global gene expression and genome-wide splicing analysis in wild-type and scr106 seedlings revealed that OsSCR106 regulates its targets, presumably through regulating the alternative 3'-splice site. Under salt stress conditions, we identified multiple splice isoforms regulated by OsSCR106. Collectively, our results suggest that OsSCR106 is an important splicing factor that plays a crucial role in accurate pre-mRNA splicing and regulates abiotic stress responses in plants.

摘要

植物利用复杂的分子机制来微调其对生长、发育和应激信号的反应。基因表达通过转录和剪接等调节过程影响植物细胞反应。前体 mRNA 通过可变剪接来增加基因组编码潜力并进一步调节表达。丝氨酸/精氨酸丰富(SR)蛋白是一类前体 mRNA 剪接因子,可识别剪接顺式元件并调节组成性和选择性剪接。已有研究报道了水稻基因组中的 SR 蛋白基因,根据其结构域结构分为六个亚家族。在这里,我们鉴定了一个具有 RNA 识别基序(RRM)和 SR-二肽的水稻新剪接因子,该因子与 SR 蛋白亚家族 SC 相关。OsSCR106 在非生物胁迫条件下调节前体 mRNA 的剪接。它定位于核斑点,这是细胞中前体 mRNA 剪接的主要部位。功能丧失的 scr106 突变体对盐、脱落酸和低温胁迫敏感,并且表现出发育异常,表现为茎和根较短。利用 OsSCR106 融合其内源启动子后的互补作用挽救了对胁迫的超敏表型。在野生型和 scr106 幼苗中进行的全局基因表达和全基因组剪接分析表明,OsSCR106 通过调节替代 3'-剪接位点来调节其靶基因。在盐胁迫条件下,我们鉴定了多个由 OsSCR106 调控的剪接异构体。总之,我们的研究结果表明,OsSCR106 是一个重要的剪接因子,在准确的前体 mRNA 剪接中发挥关键作用,并调节植物的非生物胁迫反应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/4f29adb7f2d3/erad433_fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/c9e6f62ee46a/erad433_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/8eabccd3b3c4/erad433_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/7ba91fed414e/erad433_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/42f03f1e4f6d/erad433_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/87664fad2069/erad433_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/0a67dce6c5f5/erad433_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/866a2d8d2de4/erad433_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/ae882d79c854/erad433_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/dc5dcb64062a/erad433_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/4f29adb7f2d3/erad433_fig10.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/c9e6f62ee46a/erad433_fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/8eabccd3b3c4/erad433_fig2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/7ba91fed414e/erad433_fig3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/42f03f1e4f6d/erad433_fig4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/87664fad2069/erad433_fig5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/0a67dce6c5f5/erad433_fig6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/866a2d8d2de4/erad433_fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/ae882d79c854/erad433_fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/dc5dcb64062a/erad433_fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1baa/10837019/4f29adb7f2d3/erad433_fig10.jpg

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