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视黄酸受体β2 mRNA表达的调控:5'-非翻译区编码的抑制性肽的证据。

Regulation of RAR beta 2 mRNA expression: evidence for an inhibitory peptide encoded in the 5'-untranslated region.

作者信息

Reynolds K, Zimmer A M, Zimmer A

机构信息

Unit of Developmental Biology, National Institute of Mental Health, Bethesda, Maryland 20892-4090, USA.

出版信息

J Cell Biol. 1996 Aug;134(4):827-35. doi: 10.1083/jcb.134.4.827.

Abstract

Regulation of mRNA translation and stability plays an important role in the control of gene expression during embryonic development. We have recently shown that the tissue-specific expression of the RAR beta 2 gene in mouse embryos is regulated at the translational level by short upstream open reading frames (uORFs) In the 5'-untranslated region (Zimmer, A., A.M. Zimmer, and K. Reynolds. 1994. J. Cell Biol. 127:1111-1119). To gain insight into the molecular mechanism, we have performed a systematic mutational analysis of the uORFs. Two series of constructs were tested: in one series, each uORF was individually inactivated by introducing a point mutation in its start codon; in the second series, all but one ORF were inactivated. Our results indicate that individual uORFs may have different functions. uORF4 seems to inhibit translation of the major ORF in heart and brain, while uORFs 2 and 5 appear to be important for efficient translation in all tissues. To determine whether the polypeptide encoded by uORF4 or the act of translating it, is the significant event, we introduced point mutations to create silent mutations or amino acid substitutions in uORF4. Our results indicate that the uORF4 amino acid coding sequence is important for the inhibitory effect on translation of the downstream major ORF.

摘要

mRNA翻译和稳定性的调控在胚胎发育过程中的基因表达控制中起着重要作用。我们最近发现,小鼠胚胎中RARβ2基因的组织特异性表达在翻译水平上受5'-非翻译区的短上游开放阅读框(uORF)调控(齐默尔,A.,A.M.齐默尔,和K.雷诺兹。1994。《细胞生物学杂志》127:1111 - 1119)。为深入了解其分子机制,我们对uORF进行了系统的突变分析。测试了两个系列的构建体:在一个系列中,通过在其起始密码子中引入点突变来单独使每个uORF失活;在第二个系列中,除了一个ORF外,所有其他ORF都失活。我们的结果表明,单个uORF可能具有不同的功能。uORF4似乎抑制心脏和大脑中主要ORF的翻译,而uORF2和uORF5对于所有组织中的有效翻译似乎很重要。为了确定是uORF4编码的多肽还是其翻译行为是重要事件,我们引入点突变以在uORF4中产生沉默突变或氨基酸替换。我们的结果表明,uORF4氨基酸编码序列对于对下游主要ORF翻译的抑制作用很重要。

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