Li Y, Nagayoshi S, Sugita M, Sugiura M
Center for Gene Research, Nagoya University, Japan.
Mol Gen Genet. 1993 May;239(1-2):304-9. doi: 10.1007/BF00281632.
Tobacco chloroplasts contain a family of ribonucleoproteins (RNPs) which appear to be involved in mRNA processing and splicing in chloroplasts. We have characterized a new cDNA, 33k-6, potentially encoding a tobacco 33 kDa chloroplast RNP (cp33) homologue. This cDNA has a 78 bp insertion near the 3' end with respect to previously characterized cp33 cDNAs, leading to the creation of an alternative C-terminal sequence. The cp33 protein is encoded by a single-copy nuclear gene in Nicotiana sylvestris, which contains three introns. No typical TATA box is present in the upstream region of the gene. Multiple transcription start sites are often observed for promoters lacking TATA boxes, and have been suggested in the cp33 gene. Sequence comparison revealed that the 78 bp insertion in 33k-6 is derived from the third intron of the cp33 gene which is not removed during pre-mRNA splicing. Ribonuclease protection analysis showed that the processing of the third intron is slow compared to the other introns. A possible role for the partially spliced mRNA (cp33k-6) is discussed.
烟草叶绿体含有一族核糖核蛋白(RNP),它们似乎参与叶绿体中的mRNA加工和剪接。我们鉴定了一个新的cDNA,33k - 6,它可能编码烟草33 kDa叶绿体RNP(cp33)的同源物。相对于先前鉴定的cp33 cDNA,该cDNA在3'端附近有一个78 bp的插入,导致产生了一个不同的C端序列。cp33蛋白由野生烟草中的一个单拷贝核基因编码,该基因包含三个内含子。该基因的上游区域不存在典型的TATA盒。对于缺乏TATA盒的启动子,经常会观察到多个转录起始位点,并且在cp33基因中也有此现象。序列比较显示,33k - 6中的78 bp插入源自cp33基因的第三个内含子,该内含子在mRNA前体剪接过程中未被去除。核糖核酸酶保护分析表明,与其他内含子相比,第三个内含子的加工速度较慢。本文讨论了部分剪接的mRNA(cp33k - 6)可能的作用。