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研究发生不分离的染色体上重组的方法。

Methods for studying recombination on chromosomes that undergo nondisjunction.

作者信息

Chakravarti A, Slaugenhaupt S A

机构信息

Department of Biostatistics, University of Pittsburgh, Pennsylvania 15261.

出版信息

Genomics. 1987 Sep;1(1):35-42. doi: 10.1016/0888-7543(87)90102-9.

DOI:10.1016/0888-7543(87)90102-9
PMID:3478296
Abstract

A lod score method is provided for mapping genes relative to the centromere using family data from autosomal trisomies. Such gene-centromere mapping can be performed whenever two or more members of a meiotic tetrad can be recovered. The critical mapping parameter is not the recombination value theta or the map distance omega, but the probability of nonreduction in a heterozygous host, the probability of heterozygosity (nonreduction) is 1-gamma/2 for a meiosis I error and gamma for a meiosis II error. Under various assumptions regarding chiasma interference, gamma can be related to theta and omega. We provide specific methods for estimating gamma and theta from trisomy data using maximum likelihood, so that recombination may be studied on chromosomes that underwent nondisjunction.

摘要

提供了一种对数优势计分法,用于利用常染色体三体的家系数据来绘制相对于着丝粒的基因图谱。只要能回收减数分裂四分体的两个或更多成员,就可以进行这种基因-着丝粒图谱绘制。关键的图谱参数不是重组值θ或图距ω,而是杂合宿主中不发生减数分裂的概率,对于减数分裂I错误,杂合性(不发生减数分裂)的概率为1-γ/2,对于减数分裂II错误,概率为γ。在关于交叉干涉的各种假设下,γ可以与θ和ω相关。我们提供了使用最大似然法从三体数据估计γ和θ的具体方法,以便能够研究发生了不分离的染色体上的重组情况。

相似文献

1
Methods for studying recombination on chromosomes that undergo nondisjunction.研究发生不分离的染色体上重组的方法。
Genomics. 1987 Sep;1(1):35-42. doi: 10.1016/0888-7543(87)90102-9.
2
The probability of detecting the origin of nondisjunction of autosomal trisomies.检测常染色体三体不分离起源的概率。
Am J Hum Genet. 1989 May;44(5):639-45.
3
Recombination and maternal age-dependent nondisjunction: molecular studies of trisomy 16.重组与母亲年龄相关的不分离:16三体的分子研究
Am J Hum Genet. 1995 Oct;57(4):867-74.
4
Evidence for reduced recombination on the nondisjoined chromosomes 21 in Down syndrome.唐氏综合征中21号不分离染色体上重组减少的证据。
Science. 1987 Aug 7;237(4815):652-4. doi: 10.1126/science.2955519.
5
The meiotic stage of nondisjunction in trisomy 21: determination by using DNA polymorphisms.21三体综合征中不分离的减数分裂阶段:通过使用DNA多态性进行确定
Am J Hum Genet. 1992 Mar;50(3):544-50.
6
Gene-centromere mapping and the study of non-disjunction in autosomal trisomies and ovarian teratomas.基因-着丝粒定位以及常染色体三体和卵巢畸胎瘤中不分离现象的研究。
Prog Clin Biol Res. 1989;311:45-79.
7
The origin of trisomy 22: evidence for acrocentric chromosome-specific patterns of nondisjunction.22号三体的起源:近端着丝粒染色体特异性不分离模式的证据。
Am J Med Genet A. 2007 Oct 1;143A(19):2249-55. doi: 10.1002/ajmg.a.31918.
8
Genetics and biology of human ovarian teratomas. II. Molecular analysis of origin of nondisjunction and gene-centromere mapping of chromosome I markers.
Am J Hum Genet. 1990 Oct;47(4):644-55.
9
Trisomy 21 (Down syndrome): studying nondisjunction and meiotic recombination by using cytogenetic and molecular polymorphisms that span chromosome 21.21三体综合征(唐氏综合征):利用跨越21号染色体的细胞遗传学和分子多态性研究不分离和减数分裂重组。
Am J Hum Genet. 1988 Feb;42(2):227-36.
10
DSLINK: a computer program for gene-centromere linkage analysis in families with a trisomic offspring.DSLINK:一种用于对有三体后代的家庭进行基因-着丝粒连锁分析的计算机程序。
Am J Hum Genet. 1987 Sep;41(3):350-5.

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