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首页> 外文期刊>African Journal of Biotechnology >Cloning and characterization of a y-type inactive HMW glutenin subunit gene from Triticum durum cultivar youmangbingmai
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Cloning and characterization of a y-type inactive HMW glutenin subunit gene from Triticum durum cultivar youmangbingmai

机译:硬粒小麦优曼冰麦Y型失活HMW谷蛋白亚基基因的克隆与鉴定

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摘要

The high molecular weight glutenin subunits (HMW-GS) are key factors of the breadmaking quality of common wheat flour. In the present study, one unexpressed1By?gene from?Triticum?durum?cultivar youmangbingmai was cloned and characterized. The results indicated that the silenced?1By?gene in youmangbingmai showed the highest homology to that of previously published?1By8, suggesting that the unexpressed?1By?may have originated from?1By8. However, compared to expressed?1By8, the silenced?1By?in youmangbingmai had a deletion of 247bp at 5' segment. The deletion resulted in the intact of DNA sequences responsible for signal peptide and N- terminal domains. The deletion also resulted in frameshift mutation in C-terminal domains and central region. Therefore,?1By?gene in youmangbingmai had no the typical structure as did normal HMW-GS genes and thus this gene can be not translated into normal HWM-GS. This may be the molecular mechanism of silence for?1By?gene in youmangbingmai. This molecular mechanism is different from those previously reported. Previous studies indicated that the insertion of transposon elements or the presence of premature stop codon is the molecular mechanisms responsible for silence of HWM-GS genes. Moreover, this deletion of 247 nucleotides in YMBM produced a new reading frame. This reading frame may produce a new protein, which is different from HWM-GS.
机译:高分子量谷蛋白亚基(HMW-GS)是普通小麦面粉面包品质的关键因素。在本研究中,克隆并鉴定了一种来自小麦(Triticum?durum)品种youmangbingmai的未表达的1By?基因。结果表明,幽曼冰麦中沉默的1By基因与以前发表的1By8同源性最高,表明未表达的1By可能起源于1By8。然而,与表达的“ 1By8”相比,幽曼冰麦中沉默的“ 1By”在5'区段具有247bp的缺失。缺失导致负责信号肽和N端结构域的DNA序列完整。该缺失还导致C端结构域和中央区域的移码突变。因此,尤曼冰麦中的“ 1By”基因没有正常的HMW-GS基因那样的典型结构,因此该基因不能翻译成正常的HWM-GS。这可能是幽曼冰麦中“ 1By”基因沉默的分子机制。该分子机制不同于先前报道的那些。先前的研究表明,转座子元件的插入或过早终止密码子的存在是导致HWM-GS基因沉默的分子机制。此外,YMBM中247个核苷酸的这种缺失产生了新的阅读框。该阅读框可能产生不同于HWM-GS的新蛋白质。

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