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不依赖于U1的前体mRNA剪接有助于可变剪接的调控。

U1-independent pre-mRNA splicing contributes to the regulation of alternative splicing.

作者信息

Fukumura Kazuhiro, Taniguchi Ichiro, Sakamoto Hiroshi, Ohno Mutsuhito, Inoue Kunio

机构信息

Department of Biology, Graduate School of Science, Kobe University, Nadaku, Kobe, Japan.

出版信息

Nucleic Acids Res. 2009 Apr;37(6):1907-14. doi: 10.1093/nar/gkp050. Epub 2009 Feb 3.

Abstract

U1 snRNP plays a crucial role in the 5' splice site recognition during splicing. Here we report the first example of naturally occurring U1-independent U2-type splicing in humans. The U1 components were not included in the pre-spliceosomal E complex formed on the human F1gamma (hF1gamma) intron 9 in vitro. Moreover, hF1gamma intron 9 was efficiently spliced even in U1-disrupted Xenopus oocytes as well as in U1-inactivated HeLa nuclear extracts. Finally, hF1gamma exon 9 skipping induced by an alternative splicing regulator Fox-1 was impaired when intron 9 was changed to the U1-dependent one. Our results suggest that U1-independent splicing contributes to the regulation of alternative splicing of a class of pre-mRNAs.

摘要

U1 小核核糖核蛋白颗粒(U1 snRNP)在剪接过程中对 5' 剪接位点的识别起着关键作用。在此,我们报道了人类中自然发生的不依赖 U1 的 U2 型剪接的首个实例。在体外,人 F1γ(hF1γ)内含子 9 上形成的剪接前体 E 复合物中不包含 U1 成分。此外,即使在 U1 缺失的非洲爪蟾卵母细胞以及 U1 失活的 HeLa 细胞核提取物中,hF1γ 内含子 9 也能高效剪接。最后,当内含子 9 变为依赖 U1 的内含子时,由可变剪接调节因子 Fox-1 诱导的 hF1γ 外显子 9 跳跃受到损害。我们的结果表明,不依赖 U1 的剪接有助于一类前体 mRNA 的可变剪接调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f203/2665233/6b451b3bfc47/gkp050f1.jpg

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