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玉米球蛋白1基因等位基因多态性的分子基础

Molecular basis for allelic polymorphism of the maize Globulin-1 gene.

作者信息

Belanger F C, Kriz A L

机构信息

Department of Agronomy, University of Illinois, Urbana 61801.

出版信息

Genetics. 1991 Nov;129(3):863-72. doi: 10.1093/genetics/129.3.863.

Abstract

An abundant protein in maize (Zea mays L.) embryos is a storage globulin encoded by the polymorphic Glb1 gene. Several Glb1 protein size alleles and a null allele have been described. Here we report the isolation and nucleotide sequence analysis of genomic clones corresponding to two Glb1 size alleles (Glb1-L and Glb1-S) and to the Glb1-0 null allele. The Glb1-L and Glb1-0 alleles differ from Glb1-S by the presence of small nucleotide insertions which are imperfect or perfect duplications, respectively, of adjacent sequences. In the case of Glb1-L, the insertion is in-frame and results in a protein larger than that encoded by Glb1-S, whereas in Glb1-0 the insertion causes a translational frameshift which introduces a premature termination codon. Although steady-state levels of Glb1-0 transcripts are extremely low in Glb1-0/0 embryos, nuclear transcription assays indicate that the Glb1-0 gene is transcribed at a level comparable to that of Glb1-L. This suggests that the low amounts of Glb1-0 transcripts in the cytoplasm may be due to mRNA instability.

摘要

玉米(Zea mays L.)胚中的一种丰富蛋白质是由多态性Glb1基因编码的贮藏球蛋白。已描述了几种Glb1蛋白质大小等位基因和一个无效等位基因。本文我们报道了与两个Glb1大小等位基因(Glb1-L和Glb1-S)以及Glb1-0无效等位基因相对应的基因组克隆的分离及核苷酸序列分析。Glb1-L和Glb1-0等位基因与Glb1-S的不同之处在于,分别存在小的核苷酸插入,这些插入分别是相邻序列的不完全或完全重复。就Glb1-L而言,插入是框内的,导致产生的蛋白质比Glb1-S编码的蛋白质大,而在Glb1-0中,插入导致翻译移码,引入了一个提前终止密码子。尽管在Glb1-0/0胚中Glb1-0转录本的稳态水平极低,但核转录分析表明,Glb1-0基因的转录水平与Glb1-L相当。这表明细胞质中Glb1-0转录本数量少可能是由于mRNA不稳定所致。

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本文引用的文献

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Plant Physiol. 1986 Dec;82(4):1069-75. doi: 10.1104/pp.82.4.1069.
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Eukaryotic promoters?真核生物启动子?
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