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小鼠与人之间的X连锁基因同源性。

X-linked genetic homologies between mouse and man.

作者信息

Davisson M T

机构信息

Jackson Laboratory, Bar Harbor, Maine 04609.

出版信息

Genomics. 1987 Nov;1(3):213-27. doi: 10.1016/0888-7543(87)90047-4.

DOI:10.1016/0888-7543(87)90047-4
PMID:3328737
Abstract

X-linked genes are conserved among all mammalian species, but the organization of genes on the X chromosome varies from one species to another. This review summarizes the evidence for established gene homologies between mice and human beings. It also describes genes that are possible homologies because of their locations in the human and murine X chromosomes and similarities in the phenotypes they produce. Based on current knowledge of homologous gene location, the human and murine X chromosomes appear to contain four highly conserved segments and differ in organization by only three to four simple chromosomal rearrangements.

摘要

X连锁基因在所有哺乳动物物种中都是保守的,但X染色体上基因的组织方式因物种而异。这篇综述总结了小鼠和人类之间已确定的基因同源性的证据。它还描述了由于其在人类和小鼠X染色体上的位置以及它们产生的表型相似性而可能存在同源性的基因。根据目前对同源基因位置的了解,人类和小鼠的X染色体似乎包含四个高度保守的片段,并且在组织上仅通过三到四次简单的染色体重排而有所不同。

相似文献

1
X-linked genetic homologies between mouse and man.小鼠与人之间的X连锁基因同源性。
Genomics. 1987 Nov;1(3):213-27. doi: 10.1016/0888-7543(87)90047-4.
2
Comparative maps: the mammalian jigsaw puzzle.比较图谱:哺乳动物的拼图游戏。
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Chromosome maps of man and mouse. IV.人类和小鼠的染色体图谱。IV.
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Waardenburg syndrome in man and splotch mutants in the mouse: a paradigm of the usefulness of linkage and synteny homologies in mouse and man for the genetic analysis of human congenital malformations.人类的瓦登伯革氏综合征与小鼠的斑点突变体:小鼠和人类中连锁和同线性同源性在人类先天性畸形遗传分析中的效用范例。
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Lengths of chromosomal segments conserved since divergence of man and mouse.自人类和小鼠分化以来保守的染色体片段长度。
Proc Natl Acad Sci U S A. 1984 Feb;81(3):814-8. doi: 10.1073/pnas.81.3.814.
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Chromosome maps of man and mouse, III.
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Maps of linkage and synteny homologies between mouse and man.小鼠与人之间的连锁和同线性同源性图谱。
Trends Genet. 1989 Mar;5(3):82-6. doi: 10.1016/0168-9525(89)90031-0.
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A phenotype map of the mouse X chromosome: models for human X-linked disease.小鼠X染色体的表型图谱:人类X连锁疾病的模型
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A molecular genetic linkage map of mouse chromosome 7.小鼠7号染色体的分子遗传连锁图谱。
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Malformation syndromes: a review of mouse/human homology.畸形综合征:小鼠/人类同源性综述
J Med Genet. 1988 Jul;25(7):480-7. doi: 10.1136/jmg.25.7.480.

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Genetic mapping of the X-linked dominant mutations striated (Str) and bare patches (Bpa) to a 600-kb region of the mouse X chromosome: implications for mapping human disorders in Xq28.
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Mouse homologues of human hereditary disease.人类遗传性疾病的小鼠同源物。
J Med Genet. 1994 Jan;31(1):1-19. doi: 10.1136/jmg.31.1.1.
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Mapping of loci and translocation breakpoints in Xq13: isolation of a conserved locus that maps close to CCG1 in human and mouse.Xq13中基因座和易位断点的定位:分离出一个在人和小鼠中均定位于接近CCG1的保守基因座。
Mamm Genome. 1994 Apr;5(4):237-40. doi: 10.1007/BF00360553.
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Pulse-field linkage of the P3, G6pd and Cf-8 genes on the mouse X chromosome: demonstration of synteny at the physical level.小鼠X染色体上P3、G6pd和Cf-8基因的脉冲场连锁:物理水平上的同线性证明。
Nucleic Acids Res. 1989 Feb 25;17(4):1315-26. doi: 10.1093/nar/17.4.1315.
6
Regional localization of the TIMP gene on the human X chromosome. Extension of a conserved synteny and linkage group on proximal Xp.TIMP基因在人类X染色体上的区域定位。Xp近端保守同线性和连锁群的扩展。
Hum Genet. 1989 Feb;81(3):234-8. doi: 10.1007/BF00278995.
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X-linked severe combined immunodeficiency: localization within the region Xq13.1-q21.1 by linkage and deletion analysis.X连锁重症联合免疫缺陷:通过连锁和缺失分析定位至Xq13.1-q21.1区域
Am J Hum Genet. 1989 May;44(5):724-30.
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Androgen receptor locus on the human X chromosome: regional localization to Xq11-12 and description of a DNA polymorphism.人类X染色体上的雄激素受体基因座:区域定位至Xq11 - 12及一种DNA多态性的描述。
Am J Hum Genet. 1989 Feb;44(2):264-9.
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