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抑制查尔酮合酶多基因家族表达的重复序列和恢复其表达的缺失序列

Duplications That Suppress and Deletions That Restore Expression from a Chalcone Synthase Multigene Family.

作者信息

Todd J. J., Vodkin L. O.

机构信息

Department of Crop Sciences, Edward R. Madigan Plant and Animal Biotechnology Laboratory, University of Illinois, Urbana, Illinois 61801.

出版信息

Plant Cell. 1996 Apr;8(4):687-699. doi: 10.1105/tpc.8.4.687.

Abstract

Seed coat color in soybean is determined by four alleles of the classically defined / (inhibitor) locus that controls the presence or absence as well as the spatial distribution of anthocyanin pigments in the seed coat. By analyzing spontaneous mutations of the / locus, we demonstrated that the / locus is a region of chalcone synthase (CHS) gene duplications. Paradoxically, deletions of CHS gene sequences allow higher levels of CHS mRNAs and restore pigmentation to the seed coat. The unusual nature of the / locus suggests that its dominant alleles may represent naturally occurring examples of homology-dependent gene silencing and that the spontaneous deletions erase the gene-silencing phenomena. Specifically, mutations from the dominant ii allele (yellow seed coats with pigmented hila) to the recessive i allele (fully pigmented) can be associated with the absence of a 2.3-kb Hindlll fragment that carries CHS4, a member of the multigene CHS family. Seven independent mutations exhibit deletions in the CHS4 promoter region. The dominant / allele (yellow seed coats) exhibits an extra 12.1-kb Hindlll fragment that hybridizes with both the CHS coding region and CHS1 promoter-specific probes. Mutations of the dominant / allele to the recessive i allele (pigmented seed coats) give rise to 10.4- or 9.6-kb Hindlll CHS fragments that have lost the duplicated CHS1 promoter. Finally, gene expression analysis demonstrated that heterozygous plants (I/i) with yellow seed coats have reduced mRNA levels, indicating that the 12.1-kb Hindlll CHS fragment associated with the dominant / allele inhibits pigmentation in a trans-dominant manner. Moreover, CHS gene-specific expression in seed coats shows that multiple CHS genes are expressed in seed coats.

摘要

大豆种皮颜色由经典定义的I(抑制)位点的四个等位基因决定,该位点控制种皮中花青素色素的有无以及空间分布。通过分析I位点的自发突变,我们证明I位点是查尔酮合酶(CHS)基因重复区域。矛盾的是,CHS基因序列的缺失会使CHS mRNA水平升高,并使种皮恢复色素沉着。I位点的异常性质表明其显性等位基因可能代表同源依赖性基因沉默的自然发生实例,而自发缺失消除了基因沉默现象。具体而言,从显性ii等位基因(种脐有色素沉着的黄色种皮)到隐性i等位基因(完全色素沉着)的突变可能与携带CHS4(多基因CHS家族成员)的2.3 kb HindIII片段缺失有关。七个独立突变在CHS4启动子区域表现出缺失。显性I等位基因(黄色种皮)显示出一个额外的12.1 kb HindIII片段,该片段与CHS编码区和CHS1启动子特异性探针均杂交。显性I等位基因突变为隐性i等位基因(有色素沉着的种皮)会产生10.4或9.6 kb的HindIII CHS片段,这些片段失去了重复的CHS1启动子。最后,基因表达分析表明,种皮为黄色的杂合植株(I/i)的mRNA水平降低,这表明与显性I等位基因相关的12.1 kb HindIII CHS片段以反式显性方式抑制色素沉着。此外,种皮中CHS基因特异性表达表明多个CHS基因在种皮中表达。

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