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首页> 外文期刊>Agronomie >Isolation of a chromosomally engineered durum wheat line carrying the common wheat Glu-D1d allele.
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Isolation of a chromosomally engineered durum wheat line carrying the common wheat Glu-D1d allele.

机译:携带普通小麦Glu-D1d等位基因的染色体工程硬质小麦品系的分离。

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摘要

A 1DL chromosomal segment, containing the Glu-D1d allele encoding the 5+10 HMW glutenin subunits, was transferred into the 1AL arm of a tetraploid derivative by means of ph1c induced homoeologous recombination in backcross progeny derived from an initial common wheat (Triticum aestivum) X durum wheat (T. durum) cross. The involvement of 1AL in the exchange, which could not be directly proved by the protein assay because of the null condition at the Glu-A1 locus in all durum wheat parents used, wasunequivocally demonstrated using the D genome specific, highly repeated DNA sequence pAs1 as probe in fluorescence in situ hybridization (FISH) experiments. The Glu-D1d tetraploid carrier in fact exhibits a normal 1AS and a recombined 1AL, with a distalsegment of clear 1DL origin. The difference between the FISH patterns of recombined and normal 1AL was used to discriminate homozygous from heterozygous Glu-D1d carriers already in F2 populations, in which the recombined chromosome appeared to be transmitted normally through both germlines. Preliminary tests also show no reduction in fertility due to either one or two doses of the engineered chromosome, whose impact on various pasta and bread making quality parameters will be assessed.
机译:通过ph1c诱导的回交子代中同源重组,将包含编码5 + 10 HMW谷蛋白亚基的Glu-D1d等位基因的1DL染色体片段转移到四倍体衍生物的1AL臂中X硬质小麦(T. durum)杂交。使用D基因组特异性,高度重复的DNA序列pAs1明确证明了1AL参与交换,由于所有使用的硬粒小麦亲本中Glu-A1位点的无效条件,无法通过蛋白质测定直接证明。探针在荧光原位杂交(FISH)实验中。实际上,Glu-D1d四倍体载体表现出正常的1AS和重组的1AL,远侧节段的来源明确为1DL。重组和正常1AL的FISH模式之间的差异用于区分纯合子与已经存在于F2群体中的杂合Glu-D1d携带者,其中重组染色体似乎通过两个种系正常传播。初步测试也没有显示由于一或两剂工程染色体而导致的生育力下降,将评估其对各种面食和面包制作质量参数的影响。

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