Farjo Q, Jackson A U, Xu J, Gryzenia M, Skolnick C, Agarwal N, Swaroop A
Department of Ophthalmology, Kellogg Eye Center, University of Michigan, Ann Arbor 48105.
Genomics. 1993 Nov;18(2):216-22. doi: 10.1006/geno.1993.1458.
The NRL gene (D14S46E) is expressed in cells of human retina and encodes a putative DNA-binding protein of the leucine zipper family. Here we describe the analysis of the murine homolog of the NRL gene, Nrl. Various cDNAs resulting from alternate polyadenylation are characterized. The deduced polypeptide sequence is highly conserved between mouse and human, with an identical basic motif and leucine zipper domain. The nucleotide sequences in the 5' and 3'-untranslated regions also show significant homology. The 3'-untranslated region contains a polymorphic AGG-trinucleotide repeat. The murine Nrl gene consists of three exons; of these, the first is untranslated. The 5'-upstream promoter region has no canonical TATA box, but contains consensus binding site sequences for several DNA-binding proteins. Analysis of RNA from adult mouse tissues confirms the retina-specific expression of Nrl. This study provides the basis for dissecting the cis-regulatory elements involved in the retina-specific expression and for the development of an experimental model to investigate the function or any diseases associated with this gene in humans.
NRL基因(D14S46E)在人类视网膜细胞中表达,编码一种推测的亮氨酸拉链家族DNA结合蛋白。在此,我们描述了NRL基因的小鼠同源基因Nrl的分析。对由可变聚腺苷酸化产生的各种cDNA进行了表征。推导的多肽序列在小鼠和人类之间高度保守,具有相同的基本基序和亮氨酸拉链结构域。5'和3'非翻译区的核苷酸序列也显示出显著的同源性。3'非翻译区包含一个多态性AGG三核苷酸重复序列。小鼠Nrl基因由三个外显子组成;其中第一个是未翻译的。5'上游启动子区域没有典型的TATA盒,但包含几种DNA结合蛋白的共有结合位点序列。对成年小鼠组织RNA的分析证实了Nrl的视网膜特异性表达。本研究为剖析参与视网膜特异性表达的顺式调控元件以及开发实验模型以研究该基因在人类中的功能或任何相关疾病奠定了基础。