首页> 美国卫生研究院文献>American Journal of Human Genetics >The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.
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The gene for cystathionine beta-synthase (CBS) maps to the subtelomeric region on human chromosome 21q and to proximal mouse chromosome 17.

机译:胱硫醚β-合酶(CBS)的基因定位于人类21q染色体上的亚端粒区域和近端小鼠17染色体上。

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摘要

The human gene for cystathionine beta-synthase (CBS), the enzyme deficient in classical homocystinuria, has been assigned to the subtelomeric region of band 21q22.3 by in situ hybridization of a rat cDNA probe to structurally rearranged chromosomes 21. The homologous locus in the mouse (Cbs) was mapped to the proximal half of mouse chromosome 17 by Southern analysis of Chinese hamster X mouse somatic cell hybrid DNA. Thus, CBS/Cbs and the gene for alpha A-crystalline (CRYA1/Crya-1 or Acry-1) form a conserved linkage group on human (HSA) chromosome region 21q22.3 and mouse (MMU) chromosome 17 region A-C. Features of Down syndrome (DS) caused by three copies of these genes should not be present in mice trisomic for MMU 16 that have been proposed as animal models for DS. Mice partially trisomic for MMU 16 or MMU 17 should allow gene-specific dissection of the trisomy 21 phenotype.
机译:通过将大鼠cDNA探针与结构重排的21号染色体进行原位杂交,已将人类经典胱氨酸尿酸半胱氨酸胱氨酸合酶(CBS)基因分配到21q22.3条带的亚端粒区域。通过对中国仓鼠X小鼠体细胞杂种DNA进行Southern分析,将小鼠(Cbs)定位到17号染色​​体的近端。因此,CBS / Cbs和αA晶体的基因(CRYA1 / Crya-1或Acry-1)在人(HSA)染色体区域21q22.3和小鼠(MMU)染色体17区域A-C上形成保守的连接基团。由三基因的这些基因引起的唐氏综合症(DS)的特征不应存在于MMU 16的三体小鼠中,该小鼠已被提议作为DS的动物模型。对MMU 16或MMU 17部分三体性的小鼠应允许对21三体性表型进行基因特异性解剖。

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