中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
The optional long 5 '-untranslated region of human ACAT1 mRNAs impairs the production of ACAT1 protein by promoting its mRNA decay

文献类型:期刊论文

作者Zhao, XN; Chen, J; Lei, L; Hu, GJ; Xiong, Y; Xu, JJ; Li, Q; Yang, XY; Chang, CCY; Song, BL
刊名ACTA BIOCHIMICA ET BIOPHYSICA SINICA
出版日期2009
卷号41期号:1页码:30-41
关键词human ACAT1 mRNA long 5 '-UTR mRNA stability mRNA decay ACAT1 protein production
通讯作者Song, BL (reprint author), Chinese Acad Sci, State Key Lab Mol Biol, Inst Biochem & Cell Biol, Shanghai Inst Biol Sci, Shanghai 200031, Peoples R China.,blli@sibs.ac.cn
英文摘要We have previously reported that human ACAT1 mRNAs produce the 50 kDa protein using the AUG(1397-1399) initiation codon, and also a minor 56 kDa isoform using the upstream in-frame GGC(1274-1276) initiation codon. The GGC(1274-1276) codon is located at the optional long 5'-untranslated region (5'-UTR, nt 1-1396) of the mRNAs. The DNA sequences corresponding to this 5'-UTR are located in two different chromosomes, 7 and 1. In the current work, we report that the optional long 5'-UTR significantly impairs the production of human ACAT1 protein initiated from the AUG(1397-1399) codon, mainly by promoting its mRNA decay. The western blot analyses indicated that the optional long 5'-UTR potently impaired the production of different proteins initiated from the AUG(1397-1399) codon, meaning that this impairing effect was not influenced by the 3'-UTR or the coding sequence of ACAT1 mRNA. The results of reverse transcription-quantitative polymerase chain reaction demonstrated that this 5'-UTR dramatically reduced the contents of its linked mRNAs. Analyses of the protein to mRNA ratios showed that this 5'-UTR mainly decreased its mRNA stability rather than altering its translational efficiency. We next performed the plasmid transfection experiments and used actinomycin D to inhibit transcription. The results showed that this 5'-UTR promoted its mRNA decay. Additional transfection and nucleofection experiments using RNAs prepared in vitro illustrated that, in both the cytoplasm and the nucleus of cells, the optional long 5'-UTR-linked mRNAs decayed faster than those without the link. Overall, our study brings new insight to the regulation of the human ACAT1 gene expression at the post-transcription level.
学科主题Biochemistry & Molecular Biology; Biophysics
类目[WOS]Biochemistry & Molecular Biology ; Biophysics
关键词[WOS]A-CHOLESTEROL ACYLTRANSFERASE ; 2 DIFFERENT CHROMOSOMES ; ACYL-COENZYME ; MAMMALIAN-CELLS ; IN-VITRO ; TRANSLATION INITIATION ; SECONDARY STRUCTURES ; GENE-EXPRESSION ; RICH ELEMENTS ; COA
收录类别SCI
语种英语
WOS记录号WOS:000264455000004
版本出版稿
源URL[http://202.127.25.143/handle/331003/1124]  
专题上海生化细胞研究所_上海生科院生化细胞研究所
推荐引用方式
GB/T 7714
Zhao, XN,Chen, J,Lei, L,et al. The optional long 5 '-untranslated region of human ACAT1 mRNAs impairs the production of ACAT1 protein by promoting its mRNA decay[J]. ACTA BIOCHIMICA ET BIOPHYSICA SINICA,2009,41(1):30-41.
APA Zhao, XN.,Chen, J.,Lei, L.,Hu, GJ.,Xiong, Y.,...&Li, B.(2009).The optional long 5 '-untranslated region of human ACAT1 mRNAs impairs the production of ACAT1 protein by promoting its mRNA decay.ACTA BIOCHIMICA ET BIOPHYSICA SINICA,41(1),30-41.
MLA Zhao, XN,et al."The optional long 5 '-untranslated region of human ACAT1 mRNAs impairs the production of ACAT1 protein by promoting its mRNA decay".ACTA BIOCHIMICA ET BIOPHYSICA SINICA 41.1(2009):30-41.

入库方式: OAI收割

来源:上海生物化学与细胞生物学研究所

浏览0
下载0
收藏0
其他版本

除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。