Wen Y, Li G W, Chen P, Bekhor I
Laboratory of Lens Molecular Biology, Doheny Eye Institute, Los Angeles, CA, USA.
Exp Eye Res. 1995 Jun;60(6):675-82. doi: 10.1016/s0014-4835(05)80009-0.
By methods of subtraction-hybridization of lambda ZAP cDNA libraries, prepared from 4-week-old rat lens epithelial cells (capsule) and lens fiber cells (decapsulated lens), we have isolated a specific cDNA clone whose target mRNA is about 600 b long. Northern blot hybridization analysis data showed that the target mRNA was preferentially expressed in the lens epithelial cells; it was not found in the retina or in non-ocular tissues. The complete sequence of the mRNA was obtained both by the 5' and 3' rapid amplification of cDNA ends (5'-RACE, 3'-RACE), and by sequencing of a clone containing the full-length cDNA insert. It contains 599 b. with an open reading frame at nucleotide (nt) 30 (ORF30). The base sequence appears to represent a complete sequence of the target mRNA, with a poly(A) signal at nt 563-569, and a poly(A) tail at nt 582 (GenBank accession #U15149). In situ hybridization showed that the target mRNA was localized in the anterior epithelial cells, and in the elongating cells in the bow region. The encoded protein of 57 amino acids (aa) contains a basic and an acidic domain. It is rich in leucine, which is located at the basic region of the ORF at every fourth aa, and at the acidic region at eight aa intervals. Therefore, there is a periodicity in the appearance of leucine residues in the deduced primary sequence, as has been seen in DNA binding proteins. Search of GenBank, EMBL and Swiss-Prot did not yield significant homology to any of the entered sequences in those databanks. Our data demonstrate that we have isolated a cDNA clone containing novel sequences specifically expressed in lens epithelial cells.
通过对从4周龄大鼠晶状体上皮细胞(囊膜)和晶状体纤维细胞(去囊膜晶状体)制备的λZAP cDNA文库进行消减杂交的方法,我们分离出了一个特定的cDNA克隆,其靶mRNA约600个碱基长。Northern印迹杂交分析数据表明,靶mRNA在晶状体上皮细胞中优先表达;在视网膜或非眼组织中未发现。通过cDNA末端的5'和3'快速扩增(5'-RACE,3'-RACE)以及对包含全长cDNA插入片段的克隆进行测序,获得了mRNA的完整序列。它包含599个碱基,在核苷酸(nt)30处有一个开放阅读框(ORF30)。碱基序列似乎代表了靶mRNA的完整序列,在nt 563 - 569处有一个聚腺苷酸信号,在nt 582处有一个聚腺苷酸尾(GenBank登录号#U15149)。原位杂交表明,靶mRNA定位于前上皮细胞以及弓状区域的伸长细胞中。编码的57个氨基酸(aa)的蛋白质包含一个碱性结构域和一个酸性结构域。它富含亮氨酸,在ORF的碱性区域每隔四个氨基酸出现一次,在酸性区域每隔八个氨基酸出现一次。因此,在推导的一级序列中亮氨酸残基的出现具有周期性,这在DNA结合蛋白中也有发现。在GenBank、EMBL和Swiss-Prot中搜索,未发现与这些数据库中任何输入序列有显著同源性。我们的数据表明,我们分离出了一个包含在晶状体上皮细胞中特异性表达的新序列的cDNA克隆。