White R A, Dowler L L, Pasztor L M, Gatson L L, Adkison L R, Angeloni S V, Wilson D B
Section of Genetics, Children's Mercy Hospital, UMKC School of Medicine, Kansas City, Missouri 64108, USA.
Genomics. 1995 May 1;27(1):20-6. doi: 10.1006/geno.1995.1003.
We report the mapping of the human and mouse genes for transcription factor GATA-4, a newly identified member of DNA-binding proteins involved in lineage determination. The human GATA4 gene was assigned to the short arm of human chromosome 8 using genomic DNAs from human-rodent somatic cell hybrid lines. Southern blot analyses indicated the presence of a human-specific 7.6-kb fragment that was observed only in DNA from the hybrid cells containing human chromosome 8 or the proximal region of its short arm. The mouse Gata4 gene was mapped to chromosome 14, closely linked to Clu (clusterin), using genomic DNAs from a (C57BL/6J x Mus spretus)F1 x M. spretus backcross. This mapping assignment places the Gata4 gene in the vicinity of the mouse Ds (disorganization) locus, a dominant gain-of-function mutation affecting embryonic development. We speculate that Ds is caused by a mutation in the Gata4 gene, ectopic expression of GATA-4, or a mutation in another lineage determination gene closely linked to Gata4.
我们报告了转录因子GATA-4的人类和小鼠基因定位,GATA-4是参与谱系决定的DNA结合蛋白新鉴定成员。利用人-啮齿动物体细胞杂种细胞系的基因组DNA,将人类GATA4基因定位于人类8号染色体短臂。Southern印迹分析表明存在一个人类特异性的7.6 kb片段,该片段仅在含有人类8号染色体或其短臂近端区域的杂种细胞的DNA中观察到。利用(C57BL/6J×小家鼠)F1×小家鼠回交的基因组DNA,将小鼠Gata4基因定位于14号染色体,与Clu(簇集蛋白)紧密连锁。该定位将Gata4基因置于小鼠Ds(无序)基因座附近,Ds是一种影响胚胎发育的显性功能获得性突变。我们推测Ds是由Gata4基因突变、GATA-4异位表达或与Gata4紧密连锁的另一个谱系决定基因突变引起的。