Kandala J C, Guntaka R V
Department of Molecular Microbiology and Immunology, School of Medicine, University of Missouri, Columbia 65212.
Virology. 1994 Feb;198(2):514-23. doi: 10.1006/viro.1994.1062.
A cDNA clone was isolated from a chicken embryo cDNA library employing a PCR-generated radiolabeled probe specific for the U3 region of the Rous sarcoma virus LTR. The cDNA encodes a protein of 345 aa and is homologous to the Y-box (inverted CCAAT) binding proteins. The amino acid sequence of the RSV-EF-I shows 75% identity with rat EF1 but the NH2-terminal 60-aa residues share little homology. At the carboxyl terminus an additional 28-aa sequence, rich in basic residues, probably encoded by an extra exon, is present in the chicken RSV-EF-1. Electrophoretic mobility assays carried out with various radiolabeled oligonucleotides spanning the U3 region of the RSV LTR (-234 to -54) indicated that the RSV-EF-I binds strongly to the sequence AAGGTGGTAC and somewhat less efficiently to the sequences AAGGAAAG and CTTATGCAA. In contrast to rat EF1A which binds to the inverted CCAAT box, RSV-EF-I does not bind to the CCAAT box sequence. These results suggest that the RSV-EF-I, although structurally similar to the rat EF1A, binds differently to more than one cis-acting element. The gene for RSV-EF-I is expressed in a variety of cell lines, although most abundantly in avian fibroblasts compared to mammalian cells. It is barely expressed in normal lives but expressed at significantly enhanced levels in many immortalized hepatocytes and hepatic tumors.
利用针对劳氏肉瘤病毒长末端重复序列(LTR)U3区域的PCR产生的放射性标记探针,从鸡胚cDNA文库中分离出一个cDNA克隆。该cDNA编码一个345个氨基酸的蛋白质,与Y盒(反向CCAAT)结合蛋白同源。劳氏肉瘤病毒EF-I(RSV-EF-I)的氨基酸序列与大鼠EF1有75%的同一性,但氨基末端的60个氨基酸残基同源性较低。在鸡RSV-EF-1的羧基末端存在一个额外的富含碱性残基的28个氨基酸序列,可能由一个额外的外显子编码。用跨越RSV LTR的U3区域(-234至-54)的各种放射性标记寡核苷酸进行的电泳迁移率分析表明,RSV-EF-I与序列AAGGTGGTAC强烈结合,与序列AAGGAAAG和CTTATGCAA的结合效率略低。与结合反向CCAAT框的大鼠EF1A不同,RSV-EF-I不与CCAAT框序列结合。这些结果表明,RSV-EF-I虽然在结构上与大鼠EF1A相似,但与不止一个顺式作用元件的结合方式不同。RSV-EF-I基因在多种细胞系中表达,尽管与哺乳动物细胞相比,在禽成纤维细胞中表达最为丰富。它在正常肝脏中几乎不表达,但在许多永生化肝细胞和肝肿瘤中表达水平显著提高。