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检测来自纤细裸藻叶绿体的32,000分子量类囊体膜蛋白的多个未剪接前体mRNA转录本。

Detection of multiple, unspliced precursor mRNA transcripts for the Mr 32,000 thylakoid membrane protein from Euglena gracilis chloroplasts.

作者信息

Hollingsworth M J, Johanningmeier U, Karabin G D, Stiegler G L, Hallick R B

出版信息

Nucleic Acids Res. 1984 Feb 24;12(4):2001-17. doi: 10.1093/nar/12.4.2001.

DOI:10.1093/nar/12.4.2001
PMID:6322131
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC318636/
Abstract

The psbA gene is the coding locus for a polypeptide of 32 kilodaltons that is involved in electron transport through photosystem II. The 4.9 kilobasepair (kbp) EcoRI restriction endonuclease fragment EcoI from the 145 kbp Euglena gracilis chloroplast DNA was shown to encode psbA. Five transcripts of size 3.1, 2.8, 2.3, 1.8, and 1.2 kilobases were detected by hybridization of psbA probes to nitrocellulose filter blots of electrophoretically separated RNAs. This same pattern was observed when the hybridization probe consisted of only exon sequences from this split gene. A synthetic, intron specific probe hybridized to all RNA precursors except the 1.2 kb mature RNA. These results and psbA DNA sequence data lead to the conclusion that the four higher molecular weight transcripts are unprocessed precursors of the 1.2 kilobase RNA, some of which contain unspliced intervening sequences. There is an increase in psbA transcripts during light induced maturation of the chloroplasts.

摘要

psbA基因是一个32千道尔顿多肽的编码位点,该多肽参与通过光系统II的电子传递。来自145千碱基对(kbp)的纤细裸藻叶绿体DNA的4.9千碱基对(kbp)EcoRI限制性内切酶片段EcoI被证明编码psbA。通过将psbA探针与电泳分离的RNA的硝酸纤维素滤膜杂交,检测到大小为3.1、2.8、2.3、1.8和1.2千碱基的五种转录本。当杂交探针仅由该断裂基因的外显子序列组成时,观察到相同的模式。一种合成的内含子特异性探针与除1.2 kb成熟RNA之外的所有RNA前体杂交。这些结果和psbA DNA序列数据得出结论,四种较高分子量的转录本是1.2千碱基RNA的未加工前体,其中一些含有未剪接的间隔序列。在叶绿体光诱导成熟过程中,psbA转录本增加。

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