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转座子插入导致中国小麦地方品种中Wx-B1n基因沉默。

Transposon insertion resulted in the silencing of Wx-B1n in Chinese wheat landraces.

作者信息

Zhang Ling-Ling, Chen Hu, Luo Mi, Zhang Xiao-Wei, Deng Mei, Ma Jian, Qi Peng-Fei, Wang Ji-Rui, Chen Guo-Yue, Liu Ya-Xi, Pu Zhi-En, Li Wei, Lan Xiu-Jin, Wei Yu-Ming, Zheng You-Liang, Jiang Qian-Tao

机构信息

Triticeae Research Institute, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

College of Agronomy, Sichuan Agricultural University, Chengdu, 611130, Sichuan, China.

出版信息

Theor Appl Genet. 2017 Jun;130(6):1321-1330. doi: 10.1007/s00122-017-2878-4. Epub 2017 Mar 17.

Abstract

A novel Wx-B1 allele was characterized; a transposon insertion resulted in the loss of its function, which is different from the previously reported gene silencing mechanisms at the Wx-B1 locus. The waxy protein composition of 53 Chinese wheat landraces was analyzed using sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and two-dimensional gel electrophoresis; of these, 10 did not show the expression of Wx-A1 (four accession) or Wx-B1 (six accessions) protein. The results of molecular marker detection revealed that the Wx-B1 allele (Wx-B1n) showed normal expression, inconsistent with the findings of SDS-PAGE for the Xiaobaipi accession. Further cloning of the 9160-bp region covering the Wx-B1 coding region and 3'-downstream region revealed that a 2178-bp transposon fragment had been inserted at 2462 bp within the tenth exon of Wx-B1n ORF, leading to the absence of Wx-B1 protein. Sequence analysis indicated that the insertion possessed the structural features of invert repeat and target repeat elements, we deduced that it was a transposon. Further PCR analysis revealed that this fragment had moved, but not copied itself, from 3B chromosome to the current location in Wx-B1n. Therefore, the reason for the inactivation of Wx-B1n was considerably different from those for the inactivation of Wx-B1b, Wx-B1k, and Wx-B1m; to our knowledge, this kind of structural mutation has never been reported in Wx-B1 alleles. This novel allele is interesting, because it was not associated with the deletion of other quality-related genes included in the 67 kb region lost with the common null allele Wx-B1b. The null Wx-B1n might be useful for investigating gene inactivation and expression as well as for enriching the genetic resource pool for the modification of the amylose/amylopectin ratio, thereby improving wheat quality.

摘要

鉴定出一个新的Wx-B1等位基因;转座子插入导致其功能丧失,这与之前报道的Wx-B1位点的基因沉默机制不同。使用十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和双向凝胶电泳分析了53份中国小麦地方品种的蜡质蛋白组成;其中,10份未显示Wx-A1(4份材料)或Wx-B1(6份材料)蛋白的表达。分子标记检测结果表明,Wx-B1等位基因(Wx-B1n)表现出正常表达,这与小白皮材料的SDS-PAGE结果不一致。进一步克隆覆盖Wx-B1编码区和3'下游区的9160 bp区域,结果显示在Wx-B1n ORF第十外显子内2462 bp处插入了一个2178 bp的转座子片段,导致Wx-B1蛋白缺失。序列分析表明,该插入片段具有反向重复和靶重复元件的结构特征,我们推断它是一个转座子。进一步的PCR分析表明,该片段已从3B染色体转移到Wx-B1n的当前位置,但未进行自身复制。因此,Wx-B1n失活的原因与Wx-B1b、Wx-B1k和Wx-B1m失活的原因有很大不同;据我们所知,这种结构突变在Wx-B1等位基因中从未报道过。这个新的等位基因很有趣,因为它与常见的无效等位基因Wx-B1b缺失的67 kb区域中包含的其他品质相关基因的缺失无关。无效的Wx-B1n可能有助于研究基因失活和表达,以及丰富用于改变直链淀粉/支链淀粉比例的遗传资源库,从而改善小麦品质。

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