Rodriguez A M, Rodin D, Nomura H, Morton C C, Weremowicz S, Schneider M C
Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts 02115, USA.
Genomics. 1997 Jun 15;42(3):507-13. doi: 10.1006/geno.1997.4748.
Two novel cDNAs, DNAS1L2 and DNAS1L3, are predicted to encode proteins of 299 and 305 amino acids with 56 and 46% residue identity (71 and 63% similarity), respectively, to deoxyribonuclease I (DNase I). DNAS1L2 is located on a 16p13.3 cosmid, while DNAS1L3 maps to 3p14.3-p21.1 by fluorescence in situ hybridization and by PCR analysis of a radiation hybrid panel. Northern analysis revealed DNAS1L3 expression nearly exclusively in liver, while DNAS1L2 expression was detected in brain by RT-PCR. The previously defined DNL1L or DNAS1L1 is expressed highest in heart and skeletal muscle, while DNase I is expressed in the pancreas, parotid gland, and kidney. Thus, to date, four DNase I-like genes that show different tissue expression patterns are known. A comparison of DNAS1L1, DNAS1L2, and DNAS1L3 with the well-characterized DNase I suggests that the DNAS1L proteins are unlikely to be glycosylated or bind actin; however, catalytic and calcium- and DNA-binding residues are conserved, and potentially cleavable signal peptides are present among all these proteins. This analysis also identifies regions of high conservation among these proteins with no currently assigned function.
预测有两个新的cDNA,即DNAS1L2和DNAS1L3,分别编码含299和305个氨基酸的蛋白质,它们与脱氧核糖核酸酶I(DNase I)的残基一致性分别为56%和46%(相似性分别为71%和63%)。DNAS1L2位于16p13.3黏粒上,而通过荧光原位杂交和辐射杂种板的PCR分析,DNAS1L3定位于3p14.3 - p21.1。Northern分析显示DNAS1L3几乎仅在肝脏中表达,而通过RT-PCR在脑中检测到DNAS1L2的表达。先前定义的DNL1L或DNAS1L1在心脏和骨骼肌中表达最高,而DNase I在胰腺、腮腺和肾脏中表达。因此,迄今为止,已知有四个显示不同组织表达模式的DNase I样基因。将DNAS1L1、DNAS1L2和DNAS1L3与已充分表征的DNase I进行比较表明,DNAS1L蛋白不太可能被糖基化或结合肌动蛋白;然而,催化残基、钙结合残基和DNA结合残基是保守的,并且所有这些蛋白中都存在潜在可切割的信号肽。该分析还确定了这些蛋白中具有高度保守性但目前未明确功能的区域。