PHYLOGENETIC AND STRUCTURAL-ANALYSES OF MMTV LTR ORF SEQUENCES OF EXOGENOUS AND ENDOGENOUS ORIGINS

被引:72
作者
BRANDTCARLSON, C
BUTEL, JS
WHEELER, D
机构
[1] BAYLOR COLL MED,DIV MOLEC BIOL,1 BAYLOR PLAZA,HOUSTON,TX 77030
[2] BAYLOR COLL MED,DEPT CELL BIOL,HOUSTON,TX 77030
关键词
D O I
10.1006/viro.1993.1113
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The long terminal repeat (LTR) of mouse mammary tumor virus (MMTV) harbors an open reading frame (ORF) that encodes a glycoprotein and is present in all exogenous and endogenous MMTV proviruses. The ORF protein has been reported to interact with the immune system of mice to cause deletion of specific Vβ-bearing subsets of T cells, Twenty-two MMTV LTR ORF sequences were analyzed. Although highly conserved, the MMTV ORF sequences are not identical, with ≈35% of the total variation clustered at the carboxy terminus. Statistical analysis revealed the presence of two conserved regions in the protein, one of which contained a transmembrane-like domain (residues 45-63). Two potential nuclear localization signals were recognized. Many ORF sequences shared polymorphisms. To analyze relationships, phylogenetic trees were constructed on the basis of alignments of LTR ORF sequences. A tree generated from the carboxy-terminal 35 residues clustered the sequences into three divergent families. The topology of the tree based on the amino-terminal 288 residues differed significantly, with some MMTV sequences rearranged relative to their carboxy-terminal families. A continuum of exogenous-like to endogenous-like character was suggested by the amino-terminal tree. The discordance between the topologies of the two trees suggests that some type of genetic exchange has occurred in the MMTV LTR gene. Mechanisms and implications of such genetic exchange are discussed. © 1993 Academic Press. All rights reserved.
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页码:171 / 185
页数:15
相关论文
共 68 条
[51]   ORDERED INTERSTRAND AND INTRASTRAND DNA TRANSFER DURING REVERSE TRANSCRIPTION [J].
PANGANIBAN, AT ;
FIORE, D .
SCIENCE, 1988, 241 (4869) :1064-1069
[52]   THE OPEN READING FRAMES IN THE 3' LONG TERMINAL REPEATS OF SEVERAL MOUSE MAMMARY-TUMOR VIRUS INTEGRANTS ENCODE V-BETA-3-SPECIFIC SUPERANTIGENS [J].
PULLEN, AM ;
CHOI, YW ;
KUSHNIR, E ;
KAPPLER, J ;
MARRACK, P .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (01) :41-47
[53]  
RACEVSKIS J, 1986, J VIROL, V58, P441, DOI 10.1128/JVI.58.2.441-449.1986
[54]   PROTEINS ENCODED BY THE LONG TERMINAL REPEAT REGION OF MOUSE MAMMARY-TUMOR VIRUS - IDENTIFICATION BY HYBRID-SELECTED TRANSLATION [J].
RACEVSKIS, J ;
PRAKASH, O .
JOURNAL OF VIROLOGY, 1984, 51 (03) :604-610
[55]   A HYPERCONVERSION MECHANISM GENERATES THE CHICKEN LIGHT CHAIN PREIMMUNE REPERTOIRE [J].
REYNAUD, CA ;
ANQUEZ, V ;
GRIMAL, H ;
WEILL, JC .
CELL, 1987, 48 (03) :379-388
[56]   THE RATE OF NUCLEAR CYTOPLASMIC PROTEIN-TRANSPORT IS DETERMINED BY THE CASEIN KINASE-II SITE FLANKING THE NUCLEAR-LOCALIZATION SEQUENCE OF THE SV40 T-ANTIGEN [J].
RIHS, HP ;
JANS, DA ;
FAN, H ;
PETERS, R .
EMBO JOURNAL, 1991, 10 (03) :633-639
[57]   MLS-1-LIKE SUPERANTIGEN IN THE MA MYJ MOUSE IS ENCODED BY A NEW MAMMARY-TUMOR PROVIRUS THAT IS DISTINCT FROM MTV-7 [J].
RUDY, CK ;
KRAUS, E ;
PALMER, E ;
HUBER, BT .
JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (06) :1613-1621
[58]   NAF, A TRANS-REGULATING NEGATIVE-ACTING FACTOR ENCODED WITHIN THE MOUSE MAMMARY-TUMOR VIRUS OPEN READING FRAME REGION [J].
SALMONS, B ;
ERFLE, V ;
BREM, G ;
GUNZBURG, WH .
JOURNAL OF VIROLOGY, 1990, 64 (12) :6355-6359
[59]   HOW PROTEINS ENTER THE NUCLEUS [J].
SILVER, PA .
CELL, 1991, 64 (03) :489-497
[60]   COEXPRESSION OF MMTV/V-HA-RAS AND MMTV/C-MYC GENES IN TRANSGENIC MICE - SYNERGISTIC ACTION OF ONCOGENES INVIVO [J].
SINN, E ;
MULLER, W ;
PATTENGALE, P ;
TEPLER, I ;
WALLACE, R ;
LEDER, P .
CELL, 1987, 49 (04) :465-475