生物
基因
单倍率不足
基因定位
遗传学
互补DNA
辐射混合映射
基因家族
染色体区
荧光原位杂交
染色体
位置克隆
表型
基因表达
分子生物学
作者
Minoru Horie,Mikio Suzuki,Eiichi Takáhashi,Akira Tanigami
出处
期刊:Genomics
[Elsevier]
日期:1999-09-01
卷期号:60 (2): 241-243
被引量:33
标识
DOI:10.1006/geno.1999.5887
摘要
The 14-3-3 family of proteins exerts diverse influences on the signal transduction pathways of cells. We have newly identified a human cDNA encoding the gamma subtype of the 14-3-3 family of genes. The deduced amino acid sequence of human 14-3-3gamma was identical to that of rat 14-3-3gamma. The human 14-3-3gamma gene (HGMW-approved symbol YWHAG) is highly expressed in brain, skeletal muscle, and heart. By fluorescence in situ hybridization analysis, the human 14-3-3gamma gene was mapped to chromosome 7q11.23. Radiation hybrid mapping has shown that this gene is localized 2.33 cR telomeric to D7S1870, a polymorphic marker located at the most telomeric end of the common deletion region of Williams-Beuren syndrome (WBS). This suggests that haploinsufficiency of 14-3-3gamma may not contribute to the WBS phenotype. However, information regarding the precise chromosomal location of a member of the 14-3-3 family of genes will aid in examining the relationship between this family of proteins and human disorders.
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