Strict conservation of the retroviral nucleocapsid protein zinc finger is strongly influenced by its role in viral infection processes: characterization of HIV-1 particles containing mutant nucleocapsid zinc-coordinating sequences.

The retroviral nucleocapsid (NC) protein contains highly conserved amino acid sequences (-Cys-X2-Cys-X4-His-X4-Cys-) designated retroviral (CCHC) Zn2+ fingers. The NC protein of murine leukemia viruses contains one NC Zn2+ finger and mutants that were competent in metal binding (CCCC and CCHH) packaged wild-type levels of full-length viral RNA but were not infectious. These studies were extended to human immunodeficiency virus type 1 (HIV-1), a virus with two NC Zn2+ fingers. Viruses with combinations of CCHC, CCCC, and CCHH Zn2+ fingers in each position of HIV-1 NC were characterized. Mutant particles contained the normal complement of processed viral proteins. Four mutants packaged roughly wild-type levels of genomic RNA, whereas the remaining mutants packaged reduced levels. Virions with mutated C-terminal position NC fingers were replication competent. One interesting mutant, containing a CCCC Zn2+ finger in the N-terminal position of NC, packaged wild-type levels of viral RNA and showed approximately 5% wild-type levels of infectivity when examined in CD4-expressing HeLa cells containing an HIV-1 LTR/beta-galactosidase construct. However, this particular mutant was replication defective in H9 cells; all other mutants were replication defective over the 8-week course of the assay. Two long terminal repeat viral DNA species could be detected in the CCCC mutant but not in any of the other replication-defective mutants. These studies show that the N-terminal Zn2+ finger position is more sensitive to alterations than the C-terminal position with respect to replication. Additionally, the retroviral (CCHC) NC Zn2+ finger is required for early infection processes. The evolutionary pressure to maintain CCHC NC Zn2+ fingers depends mainly on its function in infection processes, in addition to its function in genome packaging.

[1]  S. Ho,et al.  Gene splicing by overlap extension: tailor-made genes using the polymerase chain reaction. , 2013, BioTechniques.

[2]  J. Lifson,et al.  Nucleocapsid protein zinc-finger mutants of simian immunodeficiency virus strain mne produce virions that are replication defective in vitro and in vivo. , 1999, Virology.

[3]  Q. Sattentau,et al.  Inactivation of Human Immunodeficiency Virus Type 1 Infectivity with Preservation of Conformational and Functional Integrity of Virion Surface Proteins , 1998, Journal of Virology.

[4]  A. Rein,et al.  Nucleic-acid-chaperone activity of retroviral nucleocapsid proteins: significance for viral replication. , 1998, Trends in biochemical sciences.

[5]  C. Péchoux,et al.  Role of the N-Terminal Zinc Finger of Human Immunodeficiency Virus Type 1 Nucleocapsid Protein in Virus Structure and Replication , 1998, Journal of Virology.

[6]  J. Erickson,et al.  A quantum-mechanical study of metal binding sites in zinc finger structures , 1998 .

[7]  J. Lifson,et al.  Plasma SIV RNA viral load determination by real-time quantification of product generation in reverse transcriptase-polymerase chain reaction. , 1998, AIDS research and human retroviruses.

[8]  J G Levin,et al.  Human immunodeficiency virus type 1 nucleocapsid protein promotes efficient strand transfer and specific viral DNA synthesis by inhibiting TAR-dependent self-priming from minus-strand strong-stop DNA , 1997, Journal of virology.

[9]  L. Arthur,et al.  Microvesicles are a source of contaminating cellular proteins found in purified HIV-1 preparations. , 1997, Virology.

[10]  R. Gorelick,et al.  Human immunodeficiency virus type 1 nucleocapsid protein reduces reverse transcriptase pausing at a secondary structure near the murine leukemia virus polypurine tract , 1996, Journal of virology.

[11]  M. Wainberg,et al.  Human immunodeficiency virus Type 1 nucleocapsid protein (NCp7) directs specific initiation of minus-strand DNA synthesis primed by human tRNA(Lys3) in vitro: studies of viral RNA molecules mutated in regions that flank the primer binding site , 1996, Journal of virology.

[12]  R. Gorelick,et al.  HIV-1 nucleocapsid protein induces "maturation" of dimeric retroviral RNA in vitro. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[13]  L. Arthur,et al.  Genetic analysis of the zinc finger in the Moloney murine leukemia virus nucleocapsid domain: replacement of zinc-coordinating residues with other zinc-coordinating residues yields noninfectious particles containing genomic RNA , 1996, Journal of virology.

[14]  Z. Tsuchihashi,et al.  Influence of Human Immunodeficiency Virus Nucleocapsid Protein on Synthesis and Strand Transfer by the Reverse Transcriptase in Vitro(*) , 1995, The Journal of Biological Chemistry.

[15]  K. Livak,et al.  Oligonucleotides with fluorescent dyes at opposite ends provide a quenched probe system useful for detecting PCR product and nucleic acid hybridization. , 1995, PCR methods and applications.

[16]  A. Engelman,et al.  Multiple effects of mutations in human immunodeficiency virus type 1 integrase on viral replication , 1995, Journal of virology.

[17]  C. McHenry,et al.  Human immunodeficiency virus nucleocapsid protein accelerates strand transfer of the terminally redundant sequences involved in reverse transcription. , 1994, The Journal of biological chemistry.

[18]  N. Jullian,et al.  1H NMR structure and biological studies of the His23-->Cys mutant nucleocapsid protein of HIV-1 indicate that the conformation of the first zinc finger is critical for virus infectivity. , 1994, Biochemistry.

[19]  P. Brown,et al.  DNA strand exchange and selective DNA annealing promoted by the human immunodeficiency virus type 1 nucleocapsid protein , 1994, Journal of virology.

[20]  W. Fu,et al.  Characterization of human immunodeficiency virus type 1 dimeric RNA from wild-type and protease-defective virions , 1994, Journal of virology.

[21]  K. Moelling,et al.  Specific binding of HIV‐1 nucleocapsid protein to PSI RNA in vitro requires N‐terminal zinc finger and flanking basic amino acid residues. , 1994, The EMBO journal.

[22]  J. Darlix,et al.  Transactivation of the minus‐strand DNA transfer by nucleocapsid protein during reverse transcription of the retroviral genome. , 1994, The EMBO journal.

[23]  J. Luban,et al.  Mapping of functionally important residues of a cysteine-histidine box in the human immunodeficiency virus type 1 nucleocapsid protein , 1993, Journal of virology.

[24]  W. Fu,et al.  Maturation of dimeric viral RNA of Moloney murine leukemia virus , 1993, Journal of virology.

[25]  L. Arthur,et al.  The two zinc fingers in the human immunodeficiency virus type 1 nucleocapsid protein are not functionally equivalent , 1993, Journal of virology.

[26]  B. Roques,et al.  Viral RNA annealing activities of human immunodeficiency virus type 1 nucleocapsid protein require only peptide domains outside the zinc fingers. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[27]  M. Chance,et al.  Nucleocapsid zinc fingers detected in retroviruses: EXAFS studies of intact viruses and the solution‐state structure of the nucleocapsid protein from HIV‐1 , 1992, Protein science : a publication of the Protein Society.

[28]  M. Emerman,et al.  Detection of replication-competent and pseudotyped human immunodeficiency virus with a sensitive cell line on the basis of activation of an integrated beta-galactosidase gene , 1992, Journal of virology.

[29]  H. Issaq,et al.  Tightly bound zinc in human immunodeficiency virus type 1, human T-cell leukemia virus type I, and other retroviruses , 1992, Journal of virology.

[30]  A. C. Prats,et al.  Viral RNA annealing activities of the nucleocapsid protein of Moloney murine leukemia virus are zinc independent , 1991, Nucleic Acids Res..

[31]  C. Pauza Two bases are deleted from the termini of HIV-1 linear DNA during integrative recombination. , 1990, Virology.

[32]  J. Coffin,et al.  Efficient autointegration of avian retrovirus DNA in vitro , 1990, Journal of virology.

[33]  V. Vogt,et al.  Properties of avian retrovirus particles defective in viral protease , 1990, Journal of virology.

[34]  P. Dupraz,et al.  Point mutations in the proximal Cys-His box of Rous sarcoma virus nucleocapsid protein , 1990, Journal of virology.

[35]  L. Arthur,et al.  Noninfectious human immunodeficiency virus type 1 mutants deficient in genomic RNA , 1990, Journal of virology.

[36]  M. Stevenson,et al.  Integration is not necessary for expression of human immunodeficiency virus type 1 protein products , 1990, Journal of virology.

[37]  R. Young,et al.  Mutations of RNA and protein sequences involved in human immunodeficiency virus type 1 packaging result in production of noninfectious virus , 1990, Journal of virology.

[38]  S. Goff,et al.  Characterization of Moloney murine leukemia virus mutants with single-amino-acid substitutions in the Cys-His box of the nucleocapsid protein , 1989, Journal of virology.

[39]  R. Gorelick,et al.  Point mutants of Moloney murine leukemia virus that fail to package viral RNA: evidence for specific RNA recognition by a "zinc finger-like" protein sequence. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[40]  E. Gouilloud,et al.  Mutations in Rous sarcoma virus nucleocapsid protein p12 (NC): deletions of Cys-His boxes , 1988, Journal of virology.

[41]  M. Skinner,et al.  Phenotypic variation in the response to the human immunodeficiency virus among derivatives of the CEM T and WIL-2 B cell lines , 1988, The Journal of experimental medicine.

[42]  C. Gabus,et al.  Small finger protein of avian and murine retroviruses has nucleic acid annealing activity and positions the replication primer tRNA onto genomic RNA. , 1988, The EMBO journal.

[43]  D. Baltimore,et al.  Standardized and simplified nomenclature for proteins common to all retroviruses , 1988, Journal of virology.

[44]  P. Spahr,et al.  Rous sarcoma virus nucleic acid-binding protein p12 is necessary for viral 70S RNA dimer formation and packaging , 1986, Journal of virology.

[45]  H. Gendelman,et al.  Production of acquired immunodeficiency syndrome-associated retrovirus in human and nonhuman cells transfected with an infectious molecular clone , 1986, Journal of virology.

[46]  R. Gallo,et al.  Detection, isolation, and continuous production of cytopathic retroviruses (HTLV-III) from patients with AIDS and pre-AIDS. , 1984, Science.

[47]  A. van der Eb,et al.  A new technique for the assay of infectivity of human adenovirus 5 DNA. , 1973, Virology.

[48]  B. Hirt Selective extraction of polyoma DNA from infected mouse cell cultures. , 1967, Journal of molecular biology.