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小麦第一次减数分裂中 Tdes2 参与的辐射杂种 QTL 作图。

Radiation hybrid QTL mapping of Tdes2 involved in the first meiotic division of wheat.

机构信息

Department of Plant Sciences, North Dakota State University, Fargo, ND 58102, USA.

出版信息

Theor Appl Genet. 2013 Aug;126(8):1977-90. doi: 10.1007/s00122-013-2111-z. Epub 2013 May 29.

Abstract

Since the dawn of wheat cytogenetics, chromosome 3B has been known to harbor a gene(s) that, when removed, causes chromosome desynapsis and gametic sterility. The lack of natural genetic diversity for this gene(s) has prevented any attempt to fine map and further characterize it. Here, gamma radiation treatment was used to create artificial diversity for this locus. A total of 696 radiation hybrid lines were genotyped with a custom mini array of 140 DArT markers, selected to evenly span the whole 3B chromosome. The resulting map spanned 2,852 centi Ray with a calculated resolution of 0.384 Mb. Phenotyping for the occurrence of meiotic desynapsis was conducted by measuring the level of gametic sterility as seeds produced per spikelet and pollen viability at booting. Composite interval mapping revealed a single QTL with LOD of 16.2 and r (2) of 25.6 % between markers wmc326 and wPt-8983 on the long arm of chromosome 3B. By independent analysis, the location of the QTL was confirmed to be within the deletion bin 3BL7-0.63-1.00 and to correspond to a single gene located ~1.4 Mb away from wPt-8983. The meiotic behavior of lines lacking this gene was characterized cytogenetically to reveal striking similarities with mutants for the dy locus, located on the syntenic chromosome 3 of maize. This represents the first example to date of employing radiation hybrids for QTL analysis. The success achieved by this approach provides an ideal starting point for the final cloning of this interesting gene involved in meiosis of cereals.

摘要

自小麦细胞遗传学诞生以来,人们就知道 3B 染色体上携带有一个(些)基因,该基因缺失会导致染色体联会失调和配子不育。由于缺乏该基因的自然遗传多样性,因此无法对其进行精细定位和进一步表征。在这里,我们利用γ射线处理来为该基因创造人工多样性。利用 140 个 DArT 标记的定制 mini 阵列对总共 696 个辐射杂种系进行了基因型分析,这些标记均匀分布在整个 3B 染色体上。得到的图谱跨越 2852 厘镭,计算分辨率为 0.384 Mb。通过测量每个小穗产生的种子数和抽穗时花粉的活力来评估减数分裂联会失调的发生情况,从而对配子不育进行表型分析。复合区间作图揭示了一个位于 3B 染色体长臂上标记 wmc326 和 wPt-8983 之间的单个 QTL,LOD 值为 16.2,r (2)值为 25.6%。通过独立分析,确定该 QTL 的位置在缺失 bin 3BL7-0.63-1.00 内,与位于 wPt-8983 附近约 1.4 Mb 处的单个基因相对应。通过细胞学特征分析缺失该基因的系的减数分裂行为,发现与玉米同源 3 号染色体上的 dy 基因座突变体具有惊人的相似性。这是迄今为止首次利用辐射杂种进行 QTL 分析。该方法的成功为最终克隆该基因提供了理想的起点,该基因涉及到谷物的减数分裂。

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