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精细连锁图谱有助于剖析水稻种子休眠和抽穗期紧密连锁的数量性状基因座。

Fine linkage mapping enables dissection of closely linked quantitative trait loci for seed dormancy and heading in rice.

作者信息

Takeuchi Y, Lin S Y, Sasaki T, Yano M

机构信息

Institute of the Society for Techno-innovation of Agriculture, Forestry and Fisheries, 446-1 Ippaizuka, Kamiyokoba, Tsukuba, Ibaraki 305-0854, Japan.

出版信息

Theor Appl Genet. 2003 Nov;107(7):1174-80. doi: 10.1007/s00122-003-1364-3. Epub 2003 Jul 26.

DOI:10.1007/s00122-003-1364-3
PMID:12898024
Abstract

Two quantitative trait loci (QTLs) for seed dormancy (tentatively designated Sdr1) and heading date ( Hd8) have been mapped to approximately the same region on chromosome 3 by interval mapping of backcross inbred lines derived from crosses between the rice cultivars Nipponbare (japonica) and Kasalath (indica). To clarify whether Sdr1 and Hd8 could be dissected genetically, we carried out fine-scale mapping with an advanced backcross progeny. We selected a BC(4)F(1) plant, in which a small chromosomal region including Sdr1 and Hd8, on the short arm of chromosome 3, remained heterozygous, whereas all the other chromosomal regions were homozygous for Nipponbare. Days-to-heading and seed germination rate in the BC(4)F(2) plants showed continuous variation. Ten BC(4)F(2) plants with recombination in the vicinity of Sdr1 and Hd8 were selected on the basis of the genotypes of the restriction fragment length polymorphism (RFLP) markers flanking both QTLs. Genotypes of those plants for Sdr1 and Hd8 were determined by advanced progeny testing of BC(4)F(4) families. Sdr1 was mapped between the RFLP markers R10942 and C2045, and co-segregated with C1488. Hd8 was also mapped between C12534S and R10942. Six recombination events were detected between Sdr1 and Hd8. These results clearly demonstrate that Sdr1 and Hd8 were tightly linked. Nearly isogenic lines for Sdr1 and Hd8 were selected by marker-assisted selection.

摘要

通过对水稻品种日本晴(粳稻)和卡萨拉斯(籼稻)杂交衍生的回交自交系进行区间作图,已将两个控制种子休眠(暂定命名为Sdr1)和抽穗期(Hd8)的数量性状基因座(QTL)定位到第3染色体上的大致相同区域。为了阐明Sdr1和Hd8是否可以进行遗传剖析,我们利用一个高代回交后代进行了精细定位。我们选择了一株BC(4)F(1)植株,其中第3染色体短臂上包含Sdr1和Hd8的一个小染色体区域保持杂合,而所有其他染色体区域均为日本晴的纯合子。BC(4)F(2)植株的抽穗天数和种子发芽率表现出连续变异。根据两个QTL侧翼的限制性片段长度多态性(RFLP)标记的基因型,选择了10株在Sdr1和Hd8附近发生重组的BC(4)F(2)植株。通过对BC(4)F(4)家系的高代后代测试,确定了这些植株Sdr1和Hd8的基因型。Sdr1被定位在RFLP标记R10942和C2045之间,并与C1488共分离。Hd8也被定位在C12534S和R10942之间。在Sdr1和Hd8之间检测到6次重组事件。这些结果清楚地表明Sdr1和Hd8紧密连锁。通过标记辅助选择,选择了Sdr1和Hd8的近等基因系。

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