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携带对马铃薯孢囊线虫罗氏马铃薯孢囊线虫抗性的H1基因座的高分辨率图谱。

A high-resolution map of the H1 locus harbouring resistance to the potato cyst nematode Globodera rostochiensis.

作者信息

Bakker Erin, Achenbach Ute, Bakker Jeroen, van Vliet Joke, Peleman Johan, Segers Bart, van der Heijden Stefan, van der Linde Piet, Graveland Robert, Hutten Ronald, van Eck Herman, Coppoolse Eric, van der Vossen Edwin, Bakker Jaap, Goverse Aska

机构信息

Laboratory of Nematology, The Graduate School of Experimental Plant Sciences, Wageningen University, P.O. Box 8123, 6700 ES Wageningen, The Netherlands.

出版信息

Theor Appl Genet. 2004 Jun;109(1):146-52. doi: 10.1007/s00122-004-1606-z. Epub 2004 Feb 25.

Abstract

The resistance gene H1 confers resistance to the potato cyst nematode Globodera rostochiensis and is located at the distal end of the long arm of chromosome V of potato. For marker enrichment of the H1 locus, a bulked segregant analysis (BSA) was carried out using 704 AFLP primer combinations. A second source of markers tightly linked to H1 is the ultra-high-density (UHD) genetic map of the potato cross SH x RH. This map has been produced with 387 AFLP primer combinations and consists of 10,365 AFLP markers in 1,118 bins (http://www.dpw.wageningen-ur.nl/uhd/). Comparing these two methods revealed that BSA resulted in one marker/cM and the UHD map in four markers/cM in the H1 interval. Subsequently, a high-resolution genetic map of the H1 locus has been developed using a segregating F(1) SH x RH population consisting of 1,209 genotypes. Two PCR-based markers were designed at either side of the H1 gene to screen the 1,209 genotypes for recombination events. In the high-resolution genetic map, two of the four co-segregating AFLP markers could be separated from the H1 gene. Marker EM1 is located at a distance of 0.2 cM, and marker EM14 is located at a distance of 0.8 cM. The other two co-segregating markers CM1 (in coupling) and EM15 (in repulsion) could not be separated from the H1 gene.

摘要

抗病基因H1赋予马铃薯对马铃薯金线虫(Globodera rostochiensis)的抗性,位于马铃薯V号染色体长臂的远端。为了对H1位点进行标记富集,使用704对AFLP引物组合进行了混合分组分析法(BSA)。与H1紧密连锁的另一个标记来源是马铃薯杂交种SH×RH的超高密度(UHD)遗传图谱。该图谱由387对AFLP引物组合构建而成,包含1118个bin中的10365个AFLP标记(http://www.dpw.wageningen-ur.nl/uhd/)。比较这两种方法发现,在H1区间,BSA产生的标记密度为1个标记/cM,UHD图谱为4个标记/cM。随后,利用由1209个基因型组成的分离F(1) SH×RH群体构建了H1位点的高分辨率遗传图谱。在H1基因两侧设计了两个基于PCR的标记,以筛选1209个基因型中的重组事件。在高分辨率遗传图谱中,四个共分离的AFLP标记中有两个可以与H1基因分离。标记EM1位于距离H1基因0.2 cM处,标记EM14位于距离H1基因0.8 cM处。另外两个共分离标记CM1(顺式)和EM15(反式)无法与H1基因分离。

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