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利用种间杂交将Abll定位在与人类1号染色体同线的小鼠1号染色体远端保守连锁群内。

Mapping of Abll within a conserved linkage group on distal mouse chromosome 1 syntenic with human chromosome 1 using an interspecific cross.

作者信息

Seldin M F, Kruh G D

机构信息

Department of Medicine, Duke University Medical Center, Durham, North Carolina 27710.

出版信息

Genomics. 1989 Feb;4(2):221-3. doi: 10.1016/0888-7543(89)90305-4.

DOI:10.1016/0888-7543(89)90305-4
PMID:2567701
Abstract

A human Abelson related gene (ABLL) cDNA clone was used to detect restriction fragment length polymorphisms (RFLPs) on mouse Southern blots. Abll was mapped to mouse chromosome 1 by analysis of segregation with other distal chromosome 1 genetic polymorphisms by using a panel of DNAs from [(C3H/HeJ-gld/gld x Mus spretus) F1 x C3H/HeJ-gld/gld] interspecific backcross mice. The data indicate the following gene order: (centromere)-CD45-6.5 cM-Lamb-2-1 cM-Abll-2 cM-At-3. The results extend the analysis of a large conserved linkage group spanning nearly 30 cM on distal mouse chromosome 1 syntenic with human chromosome 1q21-32. Within this linkage group similar relative positions have been characterized in both species for C4BP, REN, CD45, LAMB2, ABLL, AT3, APOA2, and SPTA.

摘要

使用人类阿贝尔森相关基因(ABLL)cDNA克隆来检测小鼠Southern印迹上的限制性片段长度多态性(RFLP)。通过使用来自[(C3H/HeJ-gld/gld×小家鼠)F1×C3H/HeJ-gld/gld]种间回交小鼠的一组DNA,通过与其他1号染色体远端遗传多态性的分离分析,将Abll定位到小鼠1号染色体上。数据表明以下基因顺序:(着丝粒)-CD45-6.5厘摩-Lamb-2-1厘摩-Abll-2厘摩-At-3。这些结果扩展了对一个大型保守连锁群的分析,该连锁群跨越小鼠1号染色体远端近30厘摩,与人1号染色体q21-32同线。在这个连锁群中,C4BP、REN、CD45、LAMB2、ABLL、AT3、APOA2和SPTA在两个物种中的相对位置相似。

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Mapping of Abll within a conserved linkage group on distal mouse chromosome 1 syntenic with human chromosome 1 using an interspecific cross.利用种间杂交将Abll定位在与人类1号染色体同线的小鼠1号染色体远端保守连锁群内。
Genomics. 1989 Feb;4(2):221-3. doi: 10.1016/0888-7543(89)90305-4.
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Localization of the inhibin beta B gene on mouse chromosome 1.
抑制素βB基因在小鼠1号染色体上的定位。
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Assignment of 22 loci in the rat by somatic hybrid and linkage analysis.
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Genetic organization of complement receptor-related genes in the mouse.小鼠中补体受体相关基因的遗传组织
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Genes for two autosomal recessive forms of chronic granulomatous disease assigned to 1q25 (NCF2) and 7q11.23 (NCF1).
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