调控玉米籽粒中α-玉米蛋白和必需氨基酸积累的floury2基因的等位基因多样性和育种友好型标记的开发

IF 2.1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemical Genetics Pub Date : 2024-10-06 DOI:10.1007/s10528-024-10935-x
Hriipulou Duo, Rashmi Chhabra, Vignesh Muthusamy, Suman Dutta, Ashvinkumar Katral, Govinda Rai Sarma, Gulab Chand, Subhra J Mishra, Rajkumar U Zunjare, Firoz Hossain
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引用次数: 0

摘要

玉米玉米蛋白缺乏必需氨基酸,如蛋氨酸、赖氨酸和色氨酸。floury2(fl2)突变会减少玉米蛋白的合成,增加籽粒中蛋氨酸和赖氨酸的含量。本研究对 8 个野生型和 2 个突变型近交系的 fl2 基因(1612 bp)进行了测序,检测到 218 个 SNPs 和 18 个 InDels。在 fl2 突变体中,343 bp 处 C 到 T 的反转导致丙氨酸被缬氨酸取代。基于聚合酶链反应的标记(FL-SNP-CT)被开发出来,用于区分有利突变体 fl2 等位基因(T)和野生型 Fl2 等位基因(C)。基于基因的多样性分析使用了 7 个基于基因的 InDel 标记,将 48 个近交系分为三大群,平均遗传差异系数为 0.534。InDel 标记的平均主要等位基因频率、基因多样性、杂合度和多态性信息含量分别为 0.701、0.392、0.039 和 0.318。单倍型分析显示这 48 个近交系中 fl2 基因有 29 个单倍型。信号肽裂解位点的氨基酸替换(Ala-Val)产生了未经加工的 24 kDa 突变蛋白,而非正常基因型中的 22 kDa zein。研究中检测到的 fl2 的 8 个旁系基因在外显子长度(616-1170 bp)和翻译长度(135-267 氨基酸)方面存在差异。对 15 个高粱品种和 2 个蔗糖品种的同源物分析表明,fl2 基因的单外显子长度在 267 至 810 bp 之间。该研究阐明了 fl2 基因突变的分子基础,并为分子育种计划提供了一个育种友好型标记。这是首次在一组亚热带适应性近交系中鉴定 fl2 基因的研究。
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Allelic Diversity and Development of Breeder-Friendly Marker Specific to floury2 Gene Regulating the Accumulation of α-Zeins and Essential Amino Acids in Maize Kernel.

Maize zeins lack essential amino acids, such as methionine, lysine, and tryptophan. The floury2 (fl2) mutation reduces zein synthesis and increases methionine and lysine content in kernels. In this study, fl2 gene (1612 bp) was sequenced in eight wild-type and two mutant inbreds and detected 218 SNPs and 18 InDels. Transversion of C to T at 343 bp position caused the substitution of alanine by valine in the fl2 mutant. A PCR-based marker (FL-SNP-CT) was developed, which distinguished the favorable mutant fl2 allele (T) from the wild-type (C) Fl2 allele. Gene-based diversity analysis using seven gene-based InDel markers grouped 48 inbred lines into three major clusters, with an average genetic dissimilarity coefficient of 0.534. The average major allele frequency, gene diversity, heterozygosity, and polymorphism information content of the InDel markers were 0.701, 0.392, 0.039, and 0.318, respectively. Haplotype analysis revealed 29 haplotypes of fl2 gene among these 48 inbreds. Amino acid substitution (Ala-Val) at the signal peptide cleavage site produced unprocessed 24-kDa mutant protein instead of 22-kDa zein found in normal genotype. Eight paralogues of fl2 detected in the study showed variation in exon lengths (616-1170 bp) and translation lengths (135-267 amino acids). Orthologue analysis among 15 accessions of Sorghum bicolor and two accessions of Saccharum spontaneum revealed a single exon in fl2 gene, ranging from 267 to 810 bp. The study elucidated the molecular basis of fl2 mutation and reported a breeder-friendly marker for molecular breeding programs. This is the first study to characterize fl2 gene in a set of subtropically adapted inbreds.

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来源期刊
Biochemical Genetics
Biochemical Genetics 生物-生化与分子生物学
CiteScore
3.90
自引率
0.00%
发文量
133
审稿时长
4.8 months
期刊介绍: Biochemical Genetics welcomes original manuscripts that address and test clear scientific hypotheses, are directed to a broad scientific audience, and clearly contribute to the advancement of the field through the use of sound sampling or experimental design, reliable analytical methodologies and robust statistical analyses. Although studies focusing on particular regions and target organisms are welcome, it is not the journal’s goal to publish essentially descriptive studies that provide results with narrow applicability, or are based on very small samples or pseudoreplication. Rather, Biochemical Genetics welcomes review articles that go beyond summarizing previous publications and create added value through the systematic analysis and critique of the current state of knowledge or by conducting meta-analyses. Methodological articles are also within the scope of Biological Genetics, particularly when new laboratory techniques or computational approaches are fully described and thoroughly compared with the existing benchmark methods. Biochemical Genetics welcomes articles on the following topics: Genomics; Proteomics; Population genetics; Phylogenetics; Metagenomics; Microbial genetics; Genetics and evolution of wild and cultivated plants; Animal genetics and evolution; Human genetics and evolution; Genetic disorders; Genetic markers of diseases; Gene technology and therapy; Experimental and analytical methods; Statistical and computational methods.
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