Szpirer J, Pedeutour F, Kesti T, Riviere M, Syväoja J E, Turc-Carel C, Szpirer C
Département de Biologie Moléculaire, Universite Libre de Bruxelles, Belgium.
Genomics. 1994 Mar 15;20(2):223-6. doi: 10.1006/geno.1994.1156.
DNA polymerase epsilon [DNA pol epsilon (EC 2.7.7.7)] is one of the four nuclear DNA polymerases in eukaryotic cells. The mammalian enzyme is involved in DNA repair and possibly also in replication of chromosomal DNA. The gene encoding pol epsilon (POLE) was assigned to human and rat chromosomes 12 by Southern blot analysis of genomic DNA from mouse-human and mouse-rat somatic cell hybrid panels using human cDNA probe. The human gene was then regionally localized to band 12q24.3 by fluorescence in situ hybridization of metaphase spreads of chromosomes from human lymphocytes using genomic DNA probe. POLE is closely linked to HNF1A, a gene encoding a liver-enriched transcription factor, HNF1 alpha. The two genes thus define a new synteny group retained on human and rat chromosomes 12. Another gene mapping to the same or close-by region as human POLE is a gene for inherited disorder tuberous sclerosis 3, TSC3.
DNA聚合酶ε[DNA pol ε(EC 2.7.7.7)]是真核细胞中的四种核DNA聚合酶之一。哺乳动物的这种酶参与DNA修复,也可能参与染色体DNA的复制。通过使用人cDNA探针,对来自小鼠 - 人及小鼠 - 大鼠体细胞杂种板的基因组DNA进行Southern印迹分析,将编码pol ε(POLE)的基因定位于人及大鼠的12号染色体。然后,使用基因组DNA探针,通过对来自人淋巴细胞的染色体中期铺展进行荧光原位杂交,将人类基因区域定位到12q24.3带。POLE与HNF1A紧密连锁,HNF1A是一个编码肝脏富集转录因子HNF1α的基因。因此,这两个基因定义了一个保留在人及大鼠12号染色体上的新的同线性群。另一个定位于与人类POLE相同或附近区域的基因是遗传性疾病结节性硬化症3(TSC3)的基因。