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玉米中的三个新的显性C1抑制等位基因。

Three new dominant C1 suppressor alleles in Zea mays.

作者信息

Singer T, Gierl A, Peterson P A

机构信息

Lehrstuhl für Genetik, Technische Universität München, Germany.

出版信息

Genet Res. 1998 Apr;71(2):127-32. doi: 10.1017/s0016672398003218.

Abstract

Three new dominant suppressor mutations of the C1 transcription regulator gene in maize--C1-I delta 1, C1-I delta 2 and C1-I delta 3--are described that suppress anthocyanin colouration in kernels similar to the function of the C1-I standard inhibitor. The C1-I delta mutations were induced by imprecise excision of an En/Spm transposon in the third exon of the C1 gene. These transposon footprints cause a frameshift in the C1 open reading frame that leads to truncated proteins due to an early stop codon 30 amino acids upstream of the wild-type C1 protein. Therefore, the C1-I delta gene products lack the carboxy-terminal transcriptional activation domain of C1. The C1-I standard allele also lacks this domain and in addition differs in 17 amino acids from the wild-type C1 allele. The new C1-I delta alleles provide evidence that deletion of the carboxy-terminal activation domain alone is sufficient to generate a dominant suppressive effect on the function of wild-type C1.

摘要

本文描述了玉米中C1转录调节基因的三个新的显性抑制突变——C1-I delta 1、C1-I delta 2和C1-I delta 3,它们抑制籽粒中的花青素着色,其功能类似于C1-I标准抑制剂。C1-I delta突变是由C1基因第三外显子中En/Spm转座子的不准确切除诱导产生的。这些转座子足迹导致C1开放阅读框发生移码,由于野生型C1蛋白上游30个氨基酸处出现早期终止密码子,从而产生截短的蛋白质。因此,C1-I delta基因产物缺乏C1的羧基末端转录激活结构域。C1-I标准等位基因也缺乏该结构域,并且与野生型C1等位基因在17个氨基酸上存在差异。新的C1-I delta等位基因提供了证据,表明仅羧基末端激活结构域的缺失就足以对野生型C1的功能产生显性抑制作用。

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