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Sequence diversity of the puroindoline a and b genes in Aegilops tawsc/m-relationship tokernel texture in wheat

机译:Aegilops Tawsc / M-关系与小麦的嘌呤吲哚A和B基因的序列变化

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Puroindoline a and b (PinA, PinB) constitute the molecular-genetic basis of the Hardness locus in wheat (Triticum aestivum L.). For each, a single functional sequence is present in Chinese Spring and all soft wheats. All hard wheats have a defect in either PinA or PinB. In PinA, the defect results in the complete loss of expression. In PinB, six Single Nucleotide Polymorphisms (SNPs) result in three altered amino acids and three STOP codons. The soft PinA and PinB genes were contributed by Aegilops tauschii, the D-genome donor of wheat. Since previous studies found puroindoline sequence polymorphisms in Ae. tauschii, we undertook two surveys: one of Ae. tauschii and the second of synthetic T. durum X Ae. tauschii hexaploids produced at CIMMYT. In Ae. tauschii, seven unique gene sequences were identified among 50 accessions. Thirteen accessions possessed the same PinA and PinB sequences as soft hexaploid wheat. All were categorized as belonging to the taushcii subspecies (vs. the strangulata subsp.). Since the technological means is not available to easily measure kernel texture in Ae. tauschii, we obtained synthetic hexaploids with the aim of correlating puroindoline gene sequence and kernel texture. Classification of lines based on durum and Ae.tauschii parents showed significant differences between mean kernel texture.
机译:嘌呤吲哚啉A和B(PINA,PINB)构成小麦硬度基因座的分子遗传基础(Triticum aestivum L.)。对于每个,中国春季和所有柔软小麦的单一功能序列存在。所有硬麦在Pina或Pinb中都有缺陷。在PINA中,缺陷导致完全的表达丧失。在PINB中,六种单核苷酸多态性(SNPs)导致三个改变的氨基酸和三个止止终端。软皮和PINB基因由Aegilops Tauschii贡献,小麦的D-基因组供体。由于先前的研究发现了AE中的嘌呤啉序列多态性。 Tauschii,我们进行了两次调查:一个AE。 Tauschii和第二个合成T.Durum X AE。 Tauschii六倍体在Cimmyt生产。在AE。 Tauschii,七个独特的基因序列在50种附加方案中被鉴定出来。第十三件摘要具有与软六倍体小麦相同的Pina和Pinb序列。所有部分被分类为属于Taushcii亚种(与Strangulata subsp)。由于技术手段无法轻易测量AE中的核心纹理。 Tauschii,我们获得了合成六倍倍细性,目的是相关的嘌呤吲哚基序列和核心纹理。基于杜伦姆和AE的线分类父母的父母在平均核纹理之间存在显着差异。

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