Abstract:
:We used a series of deletion mutations in the 5' untranslated region of the prototype D type retrovirus, Mason-Pfizer Monkey Virus (MPMV), to analyse RNA encapsidation. A region was identified upstream of the major splice donor which reduced particle production but had a proportionally greater effect on RNA packaging. A small deletion downstream of the splice donor had little effect on RNA production and caused no significant packaging defect. A large deletion encompassing the end of the primer binding site down to the splice donor had a dramatic effect, disrupting viral protein synthesis. Stable cell lines were produced containing packaging-defective virus. These first-generation packaging cell lines were used to package and transfer an MPMV-based vector.
journal_name
Virologyjournal_title
Virologyauthors
Guesdon FM,Greatorex J,Rhee SR,Fisher R,Hunter E,Lever AMdoi
10.1006/viro.2001.1061subject
Has Abstractpub_date
2001-09-15 00:00:00pages
81-8issue
1eissn
0042-6822issn
1096-0341pii
S0042-6822(01)91061-Xjournal_volume
288pub_type
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