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转座元件插入在三个果蝇肌球蛋白重链突变体中重新指定了可变外显子剪接。

Transposable element insertions respecify alternative exon splicing in three Drosophila myosin heavy chain mutants.

作者信息

Davis M B, Dietz J, Standiford D M, Emerson C P

机构信息

Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, Philadephia, Pennsylvania 19104-6058, USA.

出版信息

Genetics. 1998 Nov;150(3):1105-14. doi: 10.1093/genetics/150.3.1105.

Abstract

Insertions of transposable elements into the myosin heavy chain (Mhc) locus disrupt the regulation of alternative pre-mRNA splicing for multi-alternative exons in the Mhc2, Mhc3, and Mhc4 mutants in Drosophila. Sequence and expression analyses show that each inserted element introduces a strong polyadenylation signal that defines novel terminal exons, which are then differentially recognized by the alternative splicing apparatus. Mhc2 and Mhc4 have insertion elements located within intron 7c and exon 9a, respectively, and each expresses a single truncated transcript that contains an aberrant terminal exon defined by the poly(A) signal of the inserted element and the 3' acceptor of the upstream common exon. In Mhc3, a poly(A) signal inserted into Mhc intron 7d defines terminal exons using either the upstream 3' acceptor of common exon 6 or the 7d acceptor, leading to the expression of 4.1- and 1.7-kb transcripts, respectively. Acceptor selection is regulated in Mhc3 transcripts, where the 3' acceptor of common Mhc exon 6 is preferentially selected in larvae, whereas the alternative exon 7d acceptor is favored in adults. These results reflect the adult-specific use of exon 7d and suggest that the normal exon 7 alternative splicing mechanism continues to influence the selection of exon 7d in Mhc3 transcripts. Overall, transposable element-induced disruptions in alternative processing demonstrate a role for the nonconsensus 3' acceptors in Mhc exons 7 and 9 alternative splicing regulation.

摘要

转座元件插入果蝇肌球蛋白重链(Mhc)基因座,破坏了果蝇Mhc2、Mhc3和Mhc4突变体中多个可变外显子的前体mRNA可变剪接调控。序列和表达分析表明,每个插入元件都引入了一个强聚腺苷酸化信号,该信号定义了新的末端外显子,然后可变剪接机制对其进行差异识别。Mhc2和Mhc4的插入元件分别位于内含子7c和外显子9a内,并且各自表达一个单一的截短转录本,该转录本包含由插入元件的聚腺苷酸信号和上游共同外显子的3'受体定义的异常末端外显子。在Mhc3中,插入到Mhc内含子7d中的聚腺苷酸信号使用共同外显子6的上游3'受体或7d受体来定义末端外显子,分别导致4.1 kb 和1.7 kb转录本的表达。在Mhc3转录本中受体选择受到调控,其中Mhc共同外显子6的3'受体在幼虫中优先被选择,而可变外显子7d受体在成虫中更受青睐。这些结果反映了外显子7d在成虫中的特异性使用,并表明正常的外显子7可变剪接机制继续影响Mhc3转录本中外显子7d的选择。总体而言,转座元件诱导的可变加工破坏表明了非一致性3'受体在Mhc外显子7和9可变剪接调控中的作用。

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