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国际马基因图谱研讨会报告:雄性连锁图谱

Report of the International Equine Gene Mapping Workshop: male linkage map.

作者信息

Guérin G, Bailey E, Bernoco D, Anderson I, Antczak D F, Bell K, Binns M M, Bowling A T, Brandon R, Cholewinski G, Cothran E G, Ellegren H, Förster M, Godard S, Horin P, Ketchum M, Lindgren G, McPartlan H, Mériaux J C, Mickelson J R, Millon L V, Murray J, Neau A, Røed K, Ziegle J

机构信息

INRA Centre de Recherches de Jouy, Jouy-en-Josas, France.

出版信息

Anim Genet. 1999 Oct;30(5):341-54. doi: 10.1046/j.1365-2052.1999.00510.x.

DOI:10.1046/j.1365-2052.1999.00510.x
PMID:10582279
Abstract

The goal of the First International Equine Gene Mapping Workshop, held in 1995, was the construction of a low density, male linkage map for the horse. For this purpose, the International Horse Reference Family Panel (IHRFP) was established, consisting of 12 paternal half-sib families with 448 half-sib offspring provided by 10 laboratories. Blood samples were collected and DNA extracted in each laboratory and sent to the Lexington laboratory (KY, USA) for dispatch in aliquots to 14 typing laboratories. In total, 161 markers (144 microsatellites, seven blood groups and 10 proteins) were tested for all families for which the sire was heterozygous. Genealogies and typing data were sent for analysis to the INRA laboratory (Jouy-en-Josas, France) according to a specific format and entered into a database with input verification and output processes. Linkage analysis was performed with the CRIMAP program. Significant linkage was detected for 124 loci, of which 95 were unambiguously ordered using a multipoint analysis with an average spacing of 14.2 CM. These loci were distributed among 29 linkage groups. A more comprehensive analysis including synteny group data and FISH data suggested that 26 autosomes out of 31 are covered. The complete map spans 936 CM.

摘要

1995年举办的第一届国际马基因图谱研讨会的目标是构建马的低密度雄性连锁图谱。为此,成立了国际马参考家系小组(IHRFP),该小组由12个父系半同胞家系组成,有来自10个实验室的448个半同胞后代。每个实验室采集血样并提取DNA,然后送往列克星敦实验室(美国肯塔基州),再将其分成小份发送到14个分型实验室。总共对所有父本为杂合子的家系检测了161个标记(144个微卫星、7个血型和10种蛋白质)。系谱和分型数据按照特定格式发送到法国国家农业研究院实验室(朱伊昂若萨)进行分析,并输入到一个带有输入验证和输出程序的数据库中。使用CRIMAP程序进行连锁分析。检测到124个位点存在显著连锁,其中95个位点通过多点分析明确排序,平均间距为14.2厘摩。这些位点分布在29个连锁群中。一项包括同线群数据和荧光原位杂交数据的更全面分析表明,31条常染色体中的26条被覆盖。完整的图谱跨度为936厘摩。

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