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基于微卫星的蜜蜂(西方蜜蜂)连锁图谱

A microsatellite-based linkage map of the honeybee, Apis mellifera L.

作者信息

Solignac Michel, Vautrin Dominique, Baudry Emmanuelle, Mougel Florence, Loiseau Anne, Cornuet Jean-Marie

机构信息

Laboratoire Populations, Génétique et Evolution, Centre National de la Recherche Scientifique, F91198 Gif-sur-Yvette Cedex, France.

出版信息

Genetics. 2004 May;167(1):253-62. doi: 10.1534/genetics.167.1.253.

Abstract

A linkage map for the honeybee (Apis mellifera) was constructed mainly from the progeny of two hybrid queens (A. m. ligustica x A. m. mellifera). A total of 541 loci were mapped; 474 were microsatellite loci; a few were additional bands produced during PCRs, one of the two rDNA loci (using ITS), the MDH locus, and three sex-linked markers (Q and FB loci and one RAPD band). Twenty-four linkage groups were estimated of which 5 were minute (between 7.1 and 22.8 cM) and 19 were major groups (>76.5 cM). The number of major linkage groups exceeded by three the number of chromosomes of the complement (n = 16). The sum of the lengths of all linkage groups amounts to 4061 cM to which must be added at least 320 cM to link groups in excess, making a total of at least 4381 cM. The length of the largest linkage group I was 630 cM. The average density of markers was 7.5 cM and the average resolution was about one marker every 300 kb. For most of the large groups, the centromeric region was determined genetically, as described in (accompanying article in this issue), using half-tetrad analysis of thelytokous parthenogens in which diploid restoration occurs through central fusion. Several cases of segregation distortion that appreared to result from deleterious recessives were discovered. A low positive interference was also detected.

摘要

一张蜜蜂(西方蜜蜂)的连锁图谱主要构建于两只杂交蜂王(意大利蜜蜂×西方蜜蜂)的后代。总共定位了541个位点;其中474个是微卫星位点;少数是PCR过程中产生的额外条带、两个rDNA位点之一(使用ITS)、苹果酸脱氢酶位点以及三个性连锁标记(Q和FB位点以及一个随机扩增多态性DNA条带)。估计有24个连锁群,其中5个较小(7.1至22.8厘摩),19个是主要连锁群(>76.5厘摩)。主要连锁群的数量比染色体组的染色体数(n = 16)多三个。所有连锁群的长度总和为4061厘摩,还必须至少加上320厘摩以连接多余的连锁群,总计至少4381厘摩。最大的连锁群I长度为630厘摩。标记的平均密度为7.5厘摩,平均分辨率约为每300千碱基一个标记。对于大多数大的连锁群,着丝粒区域是通过遗传方法确定的,如本期的(相关文章)所述,利用产雌孤雌生殖单倍体的半四分体分析,其中二倍体通过中央融合恢复。发现了几例似乎由有害隐性基因导致的分离畸变。还检测到较低的正干涉。

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