首页> 外文期刊>BMC Plant Biology >Loss-of-function mutations affecting a specific Glycine max R2R3 MYB transcription factor result in brown hilum and brown seed coats
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Loss-of-function mutations affecting a specific Glycine max R2R3 MYB transcription factor result in brown hilum and brown seed coats

机译:影响特定甘氨酸最大R2R3 MYB转录因子的功能丧失突变会导致棕色肺门和棕色种皮

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Background Although modern soybean cultivars feature yellow seed coats, with the only color variation found at the hila, the ancestral condition is black seed coats. Both seed coat and hila coloration are due to the presence of phenylpropanoid pathway derivatives, principally anthocyanins. The genetics of soybean seed coat and hilum coloration were first investigated during the resurgence of genetics during the 1920s, following the rediscovery of Mendel's work. Despite the inclusion of this phenotypic marker into the extensive genetic maps developed for soybean over the last twenty years, the genetic basis behind the phenomenon of brown seed coats (the R locus) has remained undetermined until now. Results In order to identify the gene responsible for the r gene effect (brown hilum or seed coat color), we utilized bulk segregant analysis and identified recombinant lines derived from a population segregating for two phenotypically distinct alleles of the R locus. Fine mapping was accelerated through use of a novel, bioinformatically determined set of Simple Sequence Repeat (SSR) markers which allowed us to delimit the genomic region containing the r gene to less than 200 kbp, despite the use of a mapping population of only 100 F6 lines. Candidate gene analysis identified a loss of function mutation affecting a seed coat-specific expressed R2R3 MYB transcription factor gene (Glyma09g36990) as a strong candidate for the brown hilum phenotype. We observed a near perfect correlation between the mRNA expression levels of the functional R gene candidate and an UDP-glucose:flavonoid 3-O-glucosyltransferase (UF3GT) gene, which is responsible for the final step in anthocyanin biosynthesis. In contrast, when a null allele of Glyma09g36990 is expressed no upregulation of the UF3GT gene was found. Conclusions We discovered an allelic series of four loss of function mutations affecting our R locus gene candidate. The presence of any one of these mutations was perfectly correlated with the brown seed coat/hilum phenotype in a broadly distributed survey of soybean cultivars, barring the presence of the epistatic dominant I allele or gray pubescence, both of which can mask the effect of the r allele, resulting in yellow or buff hila. These findings strongly suggest that loss of function for one particular seed coat-expressed R2R3 MYB gene is responsible for the brown seed coat/hilum phenotype in soybean.
机译:背景技术尽管现代大豆品种的特征是黄色种皮,但在菌丝处只有唯一的颜色变化,祖先的情况是黑色种皮。种皮和hila着色均归因于苯丙烷类途径衍生物(主要是花色苷)的存在。在孟德尔的工作重新发现之后,在1920年代的遗传学复兴期间,首次对大豆种皮和门铃色素的遗传学进行了研究。尽管在过去二十年来为大豆开发的广泛的遗传图谱中已经包含了这种表型标记,但迄今为止尚未确定棕色种皮现象(R位点)背后的遗传基础。结果为了鉴定负责r基因效应的基因(棕色门铃或种皮颜色),我们利用了大量分离子分析并鉴定了从人群中分离出的两个基因型不同的等位基因的重组株。尽管使用了仅100 F的作图群体,但通过使用新的,生物信息学确定的简单序列重复(SSR)标记集加快了精细作图,这使我们能够将包含r基因的基因组区域限定为小于200 kbp。 6 行。候选基因分析确定了影响种皮特异性表达的R2R3 MYB转录因子基因(Glyma09g36990)的功能突变丧失,该突变是棕色肺门表型的强有力候选者。我们观察到功能性R基因候选物的mRNA表达水平与UDP-葡萄糖:类黄酮3-O-葡萄糖基转移酶(UF3GT)基因之间的近乎完美的相关性,这是花色苷生物合成的最后一步。相反,当表达Glyma09g36990的无效等位基因时,未发现UF3GT基因的上调。结论我们发现了影响R基因候选基因的四个等位基因突变的等位基因序列。在广泛分布的大豆品种调查中,这些突变中任何一个的存在与棕色种皮/肺门表型完全相关,除非存在上位显性I等位基因或灰色短柔毛,这两者都可能掩盖了大豆的影响。 r等位基因,导致黄色或浅黄色hila。这些发现强烈表明,一种特定的种皮表达的R2R3 MYB基因的功能丧失是大豆中棕色种皮/肺门表型的原因。

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