bic, a novel gene activated by proviral insertions in avian leukosis virus-induced lymphomas, is likely to function through its noncoding RNA

被引:243
作者
Tam, W [1 ]
BenYehuda, D [1 ]
Hayward, WS [1 ]
机构
[1] CORNELL UNIV, GRAD SCH MED SCI, GRAD PROGRAM MOL BIOL, NEW YORK, NY 10021 USA
关键词
D O I
10.1128/MCB.17.3.1490
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The bic locus is a common retroviral integration site in avian leukosis virus (ALV)-induced B-cell lymphomas originally identified by infection of chickens with ALVs of two different subgroups(Clurman and Hayward, Mel. Cell, Biol, 9:2657-2664, 1989), Based on its frequent association with c-myc activation and its preferential activation in metastatic tumors, the bic locus is thought to harbor a gene that can collaborate with c-myc in lymphomagenesis and presumably plays a role in late stages of tumor progression. In the present study, we have cloned and characterized two novel genes, bdw and bic, at the bic locus. bdw encoded a putative novel protein of 345 amino acids, However, its expression did not appear to be altered in tumor tissues, suggesting that it is not involved in oncogenesis, The bic gene consisted of two exons and was expressed as two spliced and alternatively polyadenylated transcripts at low levels in lymphoid/hematopoietic tissues. In tumors harboring bic integrations, proviruses drove bic gene expression by promoter insertion, resulting in high levels of expression of a chimeric RNA containing bic exon 2. Interestingly, bic lacked an extensive open reading frame, implying that it may function through its RNA. Computer analysis of RNA from small exon 2 of bic predicted extensive double-stranded structures, including a highly ordered RNA duplex between nucleotides 316 and 461, The possible role of bic in cell growth and differentiation is discussed in view of the emerging evidence that untranslated RNAs play a role in growth control.
引用
收藏
页码:1490 / 1502
页数:13
相关论文
共 74 条
[1]   THE C-MYC ONCOGENE DRIVEN BY IMMUNOGLOBULIN ENHANCERS INDUCES LYMPHOID MALIGNANCY IN TRANSGENIC MICE [J].
ADAMS, JM ;
HARRIS, AW ;
PINKERT, CA ;
CORCORAN, LM ;
ALEXANDER, WS ;
CORY, S ;
PALMITER, RD ;
BRINSTER, RL .
NATURE, 1985, 318 (6046) :533-538
[2]  
ADAMS JM, 1992, CANCER SURV, V15, P119
[3]  
ALEXANDER WS, 1989, ONCOGENE, V4, P575
[4]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[5]   RETROVIRAL INSERTIONS IN THE MURINE HIS-1 LOCUS ACTIVATE THE EXPRESSION OF A NOVEL RNA THAT LACKS AN EXTENSIVE OPEN READING FRAME [J].
ASKEW, DS ;
LI, J ;
IHLE, JN .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1743-1751
[6]   FORMATION OF A TRANSFORMED FOLLICLE IS NECESSARY BUT NOT SUFFICIENT FOR DEVELOPMENT OF AN AVIAN-LEUKOSIS VIRUS-INDUCED LYMPHOMA [J].
BABA, TW ;
HUMPHRIES, EH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (01) :213-216
[7]   THE PRODUCT OF THE H19 GENE MAY FUNCTION AS AN RNA [J].
BRANNAN, CI ;
DEES, EC ;
INGRAM, RS ;
TILGHMAN, SM .
MOLECULAR AND CELLULAR BIOLOGY, 1990, 10 (01) :28-36
[8]   THE PRODUCT OF THE MOUSE XIST GENE IS A 15 KB INACTIVE X-SPECIFIC TRANSCRIPT CONTAINING NO CONSERVED ORF AND LOCATED IN THE NUCLEUS [J].
BROCKDORFF, N ;
ASHWORTH, A ;
KAY, GF ;
MCCABE, VM ;
NORRIS, DP ;
COOPER, PJ ;
SWIFT, S ;
RASTAN, S .
CELL, 1992, 71 (03) :515-526
[9]   THE HUMAN XIST GENE - ANALYSIS OF A 17 KB INACTIVE X-SPECIFIC RNA THAT CONTAINS CONSERVED REPEATS AND IS HIGHLY LOCALIZED WITHIN THE NUCLEUS [J].
BROWN, CJ ;
HENDRICH, BD ;
RUPERT, JL ;
LAFRENIERE, RG ;
XING, Y ;
LAWRENCE, J ;
WILLARD, HF .
CELL, 1992, 71 (03) :527-542
[10]   ECTOPIC EXPRESSION OF THE H19 GENE IN MICE CAUSES PRENATAL LETHALITY [J].
BRUNKOW, ME ;
TILGHMAN, SM .
GENES & DEVELOPMENT, 1991, 5 (06) :1092-1101