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节节麦新型γ-型Glu-Dt 1谷蛋白基因的鉴定与分子特征分析

Identification and molecular characterization of a novel y-type Glu-Dt 1 glutenin gene of Aegilops tauschii.

作者信息

Yan Y, Zheng J, Xiao Y, Yu J, Hu Y, Cai M, Li Y, Hsam S L K, Zeller F J

机构信息

Key Laboratory of Genetics and Biotechnology, Department of Biology, Capital Normal University, 100037 Beijing, China.

出版信息

Theor Appl Genet. 2004 May;108(7):1349-58. doi: 10.1007/s00122-003-1547-y. Epub 2004 Jan 23.

Abstract

A novel y-type high-molecular-weight glutenin subunit possessing a slightly faster mobility than that of subunit 1Dy12 in SDS-PAGE, designated 1Dy12.1(t) in Aegilops tauschi, was identified by one- and two-dimensional gel and capillary electrophoresis. Its coding gene at the Glu-D(t) 1 locus was amplified with allele-specific-PCR primers, and the amplified products were cloned and sequenced. The complete nucleotide sequence of 2,807 bp containing an open reading frame of 1,950 bp and 857 bp of upstream sequence was obtained. A perfectly conserved enhancer sequence and the -300 element were present at positions of 209-246 bp and 424-447 bp upstream of the ATG start codon, respectively. The deduced mature protein of 1 Dy12.1(t) subunit comprised 648 amino acid residues and had a Mr of 67,518 Da, which is slightly smaller than the 1Dy12 (68,695 Da) but larger than the 1Dy10 (67,495 Da) subunits of bread wheat, respectively, and corresponds well with their relative mobilities when separated by acid-PAGE. The deduced amino acid sequence indicated that the 1Dy12.1(t) subunit displayed a greater similarity to the 1Dy10 subunit, with only seven amino acid substitutions, suggesting that this novel gene could have positive effect on bread-making quality. A phenetic tree produced by nucleotide sequences showed that the x- and y-type subunit genes were respectively clustered together and that the Glu-D(t) 1y12.1 gene of Ae. tauschii is closely related to other y-type subunit genes from the B and D genomes of hexaploid bread wheat.

摘要

通过一维和二维凝胶电泳以及毛细管电泳,鉴定出一种新型的y型高分子量谷蛋白亚基,在SDS-PAGE中其迁移率略快于1Dy12亚基,在节节麦中命名为1Dy12.1(t)。用等位基因特异性PCR引物扩增其在Glu-D(t) 1位点的编码基因,并对扩增产物进行克隆和测序。获得了2807 bp的完整核苷酸序列,其中包含1950 bp的开放阅读框和857 bp的上游序列。在ATG起始密码子上游209 - 246 bp和424 - 447 bp位置分别存在一个完全保守的增强子序列和-300元件。推导的1 Dy12.1(t)亚基成熟蛋白由648个氨基酸残基组成,分子量为67518 Da,分别略小于面包小麦的1Dy12(68695 Da)但大于1Dy10(67495 Da)亚基,并且与它们在酸性PAGE分离时的相对迁移率非常吻合。推导的氨基酸序列表明,1Dy12.1(t)亚基与1Dy10亚基具有更高的相似性,仅有7个氨基酸替换,表明该新基因可能对面包制作品质有积极影响。由核苷酸序列构建的系统发育树表明,x型和y型亚基基因分别聚类在一起,节节麦的Glu-D(t) 1y12.1基因与六倍体面包小麦B和D基因组的其他y型亚基基因密切相关。

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