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Mu1玉米转座因子在两个Adh1突变体中诱导组织特异性异常剪接和多聚腺苷酸化。

The Mu1 maize transposable element induces tissue-specific aberrant splicing and polyadenylation in two Adh1 mutants.

作者信息

Ortiz D F, Strommer J N

机构信息

Department of Genetics, University of Georgia, Athens 30602.

出版信息

Mol Cell Biol. 1990 May;10(5):2090-5. doi: 10.1128/mcb.10.5.2090-2095.1990.

Abstract

Insertions of the maize transposable element Robertson's Mutator (Mu) into intron 1 of the Adh1 gene have produced a number of mutant alleles altered in quantitative expression. It has previously been shown that transcription and mRNA accumulation are reduced for two of these alleles, Adh1-S3034 and Adh1-S4477. In this report, we describe the presence of Mu1-hybridizing polyadenylated transcripts in roots of anaerobically induced seedlings of these same mutants. Sequence analysis of Mu1-hybridizing clones from a cDNA library of S3034 RNA indicated that these transcripts originated from the Adh1 locus and were produced by alternative processing of S3034 pre-mRNA. Approximately half of the cDNAs represented transcripts that had not undergone excision of the intron containing the 1.4-kilobase Mu1 insertion but were processed in response to signals present in the transposable element. Mu1 contains a donor splice site in the 5'-terminal inverted repeat that can be joined to the Adh1 exon 2 acceptor, resulting in removal of most of the Mu1 sequences from the pre-mRNA; alternatively this donor can be spliced to an acceptor within Mu1, removing an 89-nucleotide intron. Mu1 also contains polyadenylation signals that are used to produce truncated transcripts. These Mu1 transcripts produced by aberrant splicing and polyadenylation were not detected in RNA isolated from developing kernels.

摘要

玉米转座因子罗伯逊突变体(Mu)插入乙醇脱氢酶1(Adh1)基因的第1内含子,产生了一些在定量表达上发生改变的突变等位基因。此前已经表明,其中两个等位基因Adh1 - S3034和Adh1 - S4477的转录和mRNA积累减少。在本报告中,我们描述了在这些相同突变体的厌氧诱导幼苗根中存在与Mu1杂交的多聚腺苷酸化转录本。对来自S3034 RNA的cDNA文库中与Mu1杂交的克隆进行序列分析表明,这些转录本起源于Adh1基因座,是由S3034前体mRNA的可变加工产生的。大约一半的cDNA代表的转录本没有切除包含1.4千碱基Mu1插入的内含子,但根据转座元件中存在的信号进行了加工。Mu1在5'末端反向重复序列中含有一个供体剪接位点,可与Adh1外显子2受体连接,从而从前体mRNA中去除大部分Mu1序列;或者该供体可与Mu1内的一个受体剪接,去除一个89个核苷酸的内含子。Mu1还含有用于产生截短转录本的多聚腺苷酸化信号。在从发育中的籽粒中分离的RNA中未检测到由异常剪接和多聚腺苷酸化产生的这些Mu1转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/888e/360556/dd40f5751ac8/molcellb00041-0263-a.jpg

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