LOCALIZATION OF A RETROVIRAL ELEMENT WITHIN THE RD GENE CODING FOR THE BETA-SUBUNIT OF CGMP PHOSPHODIESTERASE

被引:160
作者
BOWES, C
LI, TS
FRANKEL, WN
DANCIGER, M
COFFIN, JM
APPLEBURY, ML
FARBER, DB
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,JULES STEIN EYE INST,LOS ANGELES,CA 90024
[2] UNIV CHICAGO,CTR VISUAL SCI,CHICAGO,IL 60637
[3] TUFTS UNIV,SCH MED,DEPT MOLEC BIOL,BOSTON,MA 02111
[4] TUFTS UNIV,SCH MED,DEPT MICROBIOL,BOSTON,MA 02111
[5] JACKSON LAB,BAR HARBOR,ME 04609
[6] LOYOLA MARYMOUNT UNIV,DEPT BIOL,LOS ANGELES,CA 90045
关键词
D O I
10.1073/pnas.90.7.2955
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Retinal degeneration in the rd mouse is inherited as an autosomal recessive trait and is caused by a defect in the gene encoding the beta subunit of cGMP phosphodiesterase. Recently, a close genetic association of the rd gene with an endogenous xenotropic murine leukemia virus (Xmv-28) was established by linkage analysis using recombinant inbred strains of mice. In this study, genomic DNA mapping and sequence analyses clarify the position of the proviral sequences in relation to the rd gene. We rind that the Xmv-28 provirus is integrated into intron I of the rd gene 1511 bp downstream of the exon-intron boundary. The transcriptional orientation of the provirus is opposite to that of the gene for the beta subunit of cGMP phosphodiesterase. Reverse transcription-PCR demonstrates that the integrated Xmv-28 sequences are transcribed in the retina. The provirus is present in every strain of rd mouse tested.
引用
收藏
页码:2955 / 2959
页数:5
相关论文
共 30 条
[1]   ISOLATION OF A CANDIDATE CDNA FOR THE GENE CAUSING RETINAL DEGENERATION IN THE RD MOUSE [J].
BOWES, C ;
DANCIGER, M ;
KOZAK, CA ;
FARBER, DB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :9722-9726
[2]   RETINAL DEGENERATION IN THE RD MOUSE IS CAUSED BY A DEFECT IN THE BETA-SUBUNIT OF ROD CGMP-PHOSPHODIESTERASE [J].
BOWES, C ;
LI, TS ;
DANCIGER, M ;
BAXTER, LC ;
APPLEBURY, ML ;
FARBER, DB .
NATURE, 1990, 347 (6294) :677-680
[3]  
BOWES C, 1991, INVEST OPHTHAL VIS S, V32, P572
[4]  
COFFIN JM, 1990, VIROLOGY, P1452
[5]   EXCISION OF THE DBA ECOTROPIC PROVIRUS IN DILUTE COAT-COLOR REVERTANTS OF MICE OCCURS BY HOMOLOGOUS RECOMBINATION INVOLVING THE VIRAL LTRS [J].
COPELAND, NG ;
HUTCHISON, KW ;
JENKINS, NA .
CELL, 1983, 33 (02) :379-387
[6]  
DANCIGER M, 1990, INVEST OPHTH VIS SCI, V31, P1427
[7]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[8]   RETROVIRAL INSERTIONAL MUTAGENESIS OF A TARGET ALLELE IN A HETEROZYGOUS MURINE CELL-LINE [J].
FRANKEL, W ;
POTTER, TA ;
ROSENBERG, N ;
LENZ, J ;
RAJAN, TV .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (19) :6600-6604
[9]   EFFECT OF PROVIRAL INSERTION ON TRANSCRIPTION OF THE MURINE B2MB GENE [J].
FRANKEL, WN ;
POTTER, TA ;
RAJAN, TV .
JOURNAL OF VIROLOGY, 1989, 63 (06) :2623-2628
[10]   GENETIC-ANALYSIS OF ENDOGENOUS XENOTROPIC MURINE LEUKEMIA VIRUSES - ASSOCIATION WITH 2 COMMON-MOUSE MUTATIONS AND THE VIRAL RESTRICTION LOCUS FV-1 [J].
FRANKEL, WN ;
STOYE, JP ;
TAYLOR, BA ;
COFFIN, JM .
JOURNAL OF VIROLOGY, 1989, 63 (04) :1763-1774