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序列分析参与真菌裂褶菌结实的分裂基因。

Sequence analysis of a split gene involved in fruiting from the fungus Schizophyllum commune.

机构信息

Department of Plant Physiology, Biological Centre, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands.

出版信息

EMBO J. 1984 Sep;3(9):2101-6. doi: 10.1002/j.1460-2075.1984.tb02097.x.

Abstract

The sequence of a gene and its mRNA, which is abundantly expressed during fruiting body initiation in the Basidiomycete Schizophyllum commune, is described. This gene (1G2), the first to be analyzed in this group of fungi, contains an open reading frame coding for a polypeptide of 94 amino acids and a mol. wt. of 9842. A possible signal peptide of 20 residues and one glycosylation site were found. The sequence analysis was hampered by a sequence rearrangement in one of the cDNA clones, probably due to base pairing between short complementary sequences present at the 5' and 3' ends of the mRNA. The 5' untranslated leader sequence is 57 bp long and harbors a possible ribosome binding site close to the AUG start codon. A TATA box is found at position -31 upstream of transcription initiation. The 3' untranslated sequence is 200 bp long and contains the sequence -TATATAAT-, which most likely represents the polyadenylation signal. Some heterogeneity as to the site of addition of the poly(A) tail was observed. The coding region of the gene is interrupted by three very small introns of 53, 49 and 49 bp, respectively. The 5' and 3' splice junctions are conserved: GTGAGT- and -AG-, respectively. Each intron contains a sequence complementary to the 5' end of the intron. These sequences are compared with internal conserved sequences in yeast and filamentous fungi with regard to their possible role in splicing.

摘要

描述了在担子菌 Schizophyllum commune 中,生殖体起始时大量表达的基因及其 mRNA 的序列。该基因(1G2)是该真菌群中第一个被分析的基因,包含一个开放阅读框,编码一个 94 个氨基酸的多肽和分子量为 9842 的多肽。发现了一个可能的 20 个氨基酸的信号肽和一个糖基化位点。由于 mRNA 的 5'和 3'末端存在短的互补序列配对,一个 cDNA 克隆中的序列重排阻碍了序列分析。5'非翻译先导序列长 57bp,在靠近 AUG 起始密码子的位置可能存在一个核糖体结合位点。在转录起始点上游 -31 位置发现了一个 TATA 盒。3'非翻译序列长 200bp,包含序列 -TATATAAT-,它很可能代表多聚腺苷酸化信号。观察到添加多(A)尾的位点存在一些异质性。基因的编码区被三个分别为 53、49 和 49bp 的非常小的内含子打断。5'和 3'剪接接头是保守的:GTGAGT-和 -AG-,分别为。每个内含子都包含与内含子 5'端互补的序列。这些序列与酵母和丝状真菌中的内部保守序列进行了比较,以探讨它们在剪接中的可能作用。

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本文引用的文献

1
Are snRNPs involved in splicing?小核核糖核蛋白颗粒参与剪接过程吗?
Nature. 1980 Jan 10;283(5743):220-4. doi: 10.1038/283220a0.
4
A catalogue of splice junction sequences.剪接连接序列目录。
Nucleic Acids Res. 1982 Jan 22;10(2):459-72. doi: 10.1093/nar/10.2.459.
6
Variation in the polyadenylylation site of bovine prolactin mRNA.牛催乳素mRNA聚腺苷酸化位点的变异
Proc Natl Acad Sci U S A. 1982 Jan;79(2):223-7. doi: 10.1073/pnas.79.2.223.

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