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排除酗酒与4号染色体长臂上MNS血型区域在复杂家系中的连锁关系。

Exclusion of linkage between alcoholism and the MNS blood group region on chromosome 4q in multiplex families.

作者信息

Neiswanger K, Kaplan B, Hill S Y

机构信息

Department of Psychiatry, University of Pittsburgh School of Medicine, Pennsylvania, USA.

出版信息

Am J Med Genet. 1995 Feb 27;60(1):72-9. doi: 10.1002/ajmg.1320600113.

Abstract

Polymorphic DNA markers on the long arm of chromosome 4 were used to examine linkage to alcoholism in 20 multiplex pedigrees. Fifteen loci were determined for 124 individuals. Lod scores were calculated assuming both dominant and recessive disease modes of inheritance, utilizing incidence data by age and gender that allow for correction for variable age of onset and frequency of the disorder by gender. Under the assumption that alcoholism is homogeneous in this set of pedigrees, and that a recessive mode with age and gender correction is the most appropriate, the total lod scores for all families combined were uniformly lower than -2.0. This suggests an absence of linkage between the putative alcoholism susceptibility gene and markers in the region of the MNS blood group (4q28-31), a region for which we had previously found suggestive evidence of linkage to alcoholism. The 100 cM span of chromosome 4 studied includes the class I alcohol dehydrogenase (ADH) loci. Using the recessive mode, no evidence for linkage to alcoholism was found for the markers tested, which spanned almost the entire long arm of chromosome 4. Under the dominant mode, no evidence for linkage could be found for several of the markers.

摘要

利用位于4号染色体长臂上的多态性DNA标记,对20个多重家系进行了与酒精中毒的连锁分析。为124名个体确定了15个基因座。假定疾病的遗传模式为显性和隐性,利用按年龄和性别划分的发病率数据计算优势对数(Lod)分数,这些数据可对发病年龄的变化和疾病在不同性别中的发病率进行校正。假设在这组家系中酒精中毒具有同质性,且校正年龄和性别的隐性模式最为合适,那么所有家系合并后的总Lod分数均统一低于-2.0。这表明在MNS血型区域(4q28 - 31)中,假定的酒精中毒易感基因与标记之间不存在连锁关系,而我们之前曾在该区域发现过与酒精中毒存在连锁的提示性证据。所研究的4号染色体100厘摩跨度区域包括Ⅰ类乙醇脱氢酶(ADH)基因座。采用隐性模式时,对于所检测的标记,未发现与酒精中毒存在连锁的证据,这些标记几乎覆盖了4号染色体的整个长臂。采用显性模式时,部分标记也未发现存在连锁的证据。

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