Abstract:
:Viral expression was analyzed in ten cell clones of a Friend erythroleukemia cell line (HFL/b cell line [3]), which had lost its capacity to produce infectious particles. All the ten subclones were non producers but expressed spleen focus forming virus (SFFV) polypeptides in the form of p48-p50gag and gp50-gp52env. One subclone (subclone 9) expressed the gp70env of the Friend-MuLV helper component of the Friend virus complex. Comparative analysis of viral RNA expression in one gp70- subclone (subclone 2) and in the gp70+ subclone (subclone 9) was performed using specific ecotropic env gene probe and MCF/xenotropic env gene probe. In both subclones 2 and 9, the MCF/xenotropic env gene probe detected 32S SFFV genomic RNA, 20S SFFV env gene mRNA and a 34S RNA. The ecotropic env probe failed to characterize any 38S F-MuLV genomic RNA in both clones but detected 34S RNA and 24S env mRNA in the gp70+ subclone 9. These data show that expression of a complete F-MuLV genome is not required for synthesis of env gene products.
journal_name
Biochimiejournal_title
Biochimieauthors
Moreau-Gachelin F,Robert-Lezenes J,Mathieu-Mahul D,Gisselbrecht S,Larsen CJdoi
10.1016/s0300-9084(83)80277-6subject
Has Abstractpub_date
1983-04-01 00:00:00pages
259-66issue
4-5eissn
0300-9084issn
1638-6183pii
S0300-9084(83)80277-6journal_volume
65pub_type
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