Cerritelli S M, Crouch R J
Laboratory of Molecular Genetics, National Institute of Child Health and Human Development, Bethesda, Maryland, 20892, USA.
Genomics. 1998 Nov 1;53(3):300-7. doi: 10.1006/geno.1998.5497.
We identified two human sequences and one mouse sequence in the database of expressed sequence tags that are highly homologous to the N-terminal sequence of eukaryotic RNases H1. The cDNAs for human RNASEH1 and mouse Rnaseh1 were obtained, their nucleotide sequences determined, and the proteins expressed in Escherichia coli and partially purified. Both proteins have RNase H activity in vitro and they bind to dsRNA and RNA-DNA hybrids through the N-terminal conserved motif present in eukaryotic RNases H1. The RNASEH1 gene is expressed in all human tissues at similar levels, indicating that RNase H1 may be a housekeeping protein. The human RNASEH1 and mouse Rnaseh1 cDNAs were used to isolate BAC genomic clones that were used as probes for fluorescence in situ hybridization. The human gene was localized to chromosome 17p11.2 and the mouse gene to a nonsyntenic region on chromosome 12A3. The chromosomal location and possible disease association of the human RNASEH1 gene are discussed.
我们在表达序列标签数据库中鉴定出两条人类序列和一条小鼠序列,它们与真核核糖核酸酶H1的N端序列高度同源。获得了人类RNASEH1和小鼠Rnaseh1的cDNA,测定了它们的核苷酸序列,并在大肠杆菌中表达了相应蛋白质并进行了部分纯化。两种蛋白质在体外均具有核糖核酸酶H活性,并且它们通过真核核糖核酸酶H1中存在的N端保守基序与双链RNA和RNA-DNA杂交体结合。RNASEH1基因在所有人类组织中以相似水平表达,表明核糖核酸酶H1可能是一种管家蛋白。人类RNASEH1和小鼠Rnaseh1的cDNA被用于分离BAC基因组克隆,这些克隆被用作荧光原位杂交的探针。人类基因定位于17号染色体p11.2,小鼠基因定位于12A3染色体上的一个非同源区域。本文讨论了人类RNASEH1基因的染色体定位及其可能的疾病关联。