HUMAN ENDOGENOUS RETROVIRAL ELEMENT K10 (HERV-K10) ENCODES A FULL-LENGTH GAG HOMOLOGOUS 73-KDA PROTEIN AND A FUNCTIONAL PROTEASE

被引:81
作者
MUELLERLANTZSCH, N
SAUTER, M
WEISKIRCHER, A
KRAMER, K
BEST, B
BUCK, M
GRASSER, F
机构
[1] Abteilung Virologie, Institut für Medizinische Mikrobiologie und Hygiene, Universitätskliniken des Saarlandes, 6650 Homburg/Saar
关键词
D O I
10.1089/aid.1993.9.343
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The gag-homologous region of the human endogenous retrovirus K10 (HERV-K10) was amplified by PCR from human genomic DNA and was analyzed by DNA cloning, sequencing, and expression of open reading frames in the prokaryotic pATH expression system. The analysis of genomic DNA of three donors provided evidence that HERV-K10 genes contain an open reading frame of 1966 bp spanning the entire gag-homologous region. In the prokaryotic system the entire reading frame of the HERV-K10 gag gene could be expressed as a fusion protein exhibiting a molecular weight of about 110,000. In addition, when the gag-homologous region and the adjacent HERV-K10 protease gene were prokaryotically expressed, we observed a Gag-protease fusion protein that exhibited specific autoproteolytic activities and processing of HERV-K10 Gag protein. By introducing deletions on the right end of the putative protease gene an autocatalytic site could be localized within 300 bp of the putative HERV-K10 protease gene. For the first time, these results provide evidence that the HERV-K10 encodes a full-length Gag protein and a functional protease.
引用
收藏
页码:343 / 350
页数:8
相关论文
共 32 条
[1]  
[Anonymous], 1989, MOL CLONING
[2]   ISOLATION OF MUTANTS OF HUMAN-IMMUNODEFICIENCY-VIRUS PROTEASE BASED ON THE TOXICITY OF THE ENZYME IN ESCHERICHIA-COLI [J].
BAUM, EZ ;
BEBERNITZ, GA ;
GLUZMAN, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5573-5577
[3]   SUPERCOIL SEQUENCING - A FAST AND SIMPLE METHOD FOR SEQUENCING PLASMID DNA [J].
CHEN, EY ;
SEEBURG, PH .
DNA-A JOURNAL OF MOLECULAR & CELLULAR BIOLOGY, 1985, 4 (02) :165-170
[4]   EXPRESSION OF HUMAN SEQUENCES RELATED TO THOSE OF MOUSE MAMMARY-TUMOR VIRUS [J].
FRANKLIN, GC ;
CHRETIEN, S ;
HANSON, IM ;
ROCHEFORT, H ;
MAY, FEB ;
WESTLEY, BR .
JOURNAL OF VIROLOGY, 1988, 62 (04) :1203-1210
[5]  
GRASSER FA, 1991, J VIROL, V65, P3779
[6]   PROTEOLYTIC PROCESSING OF POLYPROTEINS IN THE REPLICATION OF RNA VIRUSES [J].
HELLEN, CUT ;
KRAUSSLICH, HG ;
WIMMER, E .
BIOCHEMISTRY, 1989, 28 (26) :9881-9890
[7]   EXPRESSION OF THE ROUS-SARCOMA VIRUS POL GENE BY RIBOSOMAL FRAMESHIFTING [J].
JACKS, T ;
VARMUS, HE .
SCIENCE, 1985, 230 (4731) :1237-1242
[8]   TISSUE-SPECIFIC EXPRESSION OF HUMAN PROVIRUS ERV3 MESSENGER-RNA IN HUMAN-PLACENTA - 2 OF THE 3 ERV3 MESSENGER-RNAS CONTAIN HUMAN CELLULAR SEQUENCES [J].
KATO, N ;
PFEIFEROHLSSON, S ;
KATO, M ;
LARSSON, E ;
RYDNERT, J ;
OHLSSON, R ;
COHEN, M .
JOURNAL OF VIROLOGY, 1987, 61 (07) :2182-2191
[9]  
KOERNER TJ, 1991, METHOD ENZYMOL, V194, P477
[10]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+