Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
10
pubmed:dateCreated
1996-11-22
pubmed:abstractText
Interaction of the human immunodeficiency virus type 1 (HIV-1) Gag precursor polyprotein (Pr55Gag) with the viral genomic RNA is required for retroviral replication. Mutations that reduce RNA packaging efficiency have been localized to the highly basic nucleocapsid (NC) p7 domain of Pr55Gag, but the importance of the basic amino acid residues in specific viral RNA encapsidation and infectivity has not been thoroughly investigated in vivo. We have systematically substituted the positively charged residues of the NC domain of Pr55Gag in an HIV-1 viral clone by using alanine scanning mutagenesis and have assayed the effects of these mutations on virus replication, particle formation, and RNA packaging in vivo. Analysis of viral clones with single substitutions revealed that certain charged amino acid residues are more critical for RNA packaging efficiency and infectivity than others. Analysis of viral clones with multiple substitutions indicates that the presence of positive charge in each of three independent domains--the zinc-binding domains, the basic region that links them, and the residues that Hank the two zinc-binding domains--is necessary for efficient HIV-1 RNA packaging. Finally, we note that some mutations affect virus replication more drastically than RNA incorporation, providing in vivo evidence for the hypothesis that NC p7 may be involved in aspects of the HIV life cycle in addition to RNA packaging.
pubmed:grant
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-1427032, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-1551877, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-1631144, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2026604, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2033671, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2109098, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2191147, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2410792, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2421409, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2435721, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2451755, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2458920, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2471267, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2477156, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-2578615, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-3039161, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-3159089, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-3638988, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-5432063, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-6200935, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7523570, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7637017, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7666546, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7666550, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7666564, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7751690, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7853517, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-7888208, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8032280, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8057466, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8057495, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8083960, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8156990, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8230441, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-83199, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8350405, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8371356, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8380458, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8383840, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8474159, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8474334, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8510214, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8551614, http://linkedlifedata.com/resource/pubmed/commentcorrection/8794295-8642691
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Oct
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
70
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
6607-16
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
1996
pubmed:articleTitle
Charged amino acid residues of human immunodeficiency virus type 1 nucleocapsid p7 protein involved in RNA packaging and infectivity.
pubmed:affiliation
Department of Medicine, Children's Hospital, Boston, Massachusetts 02115, USA.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.