» Articles » PMID: 9343228

Determination of the Secondary Structure of and Cellular Protein Binding to the 3'-untranslated Region of the Hepatitis C Virus RNA Genome

Overview
Journal J Virol
Date 1997 Oct 29
PMID 9343228
Citations 84
Authors
Affiliations
Soon will be listed here.
Abstract

Hepatitis C virus (HCV) contains a positive-stranded RNA genome of approximately 9.5 kb. Despite the overall sequence diversity among individual HCV isolates, the 3'-end 98 nucleotides (nt) of the HCV RNA, which constitute part of the 3'-untranslated region (3'-UTR), are highly conserved. This conserved region may contain the cis-acting signals for RNA replication involving possibly both viral and cellular proteins. We carried out RNase digestion studies, which revealed that this 98-nt region contains three stem-loops but may also assume alternative structures. We further performed UV cross-linking experiments to detect cellular proteins that bound to this region. A 58-kDa cellular protein (p58) was detected. Its binding site was mapped to the stem-loops 2 and 3, which are the most conserved region of the 3'-UTR. Site-directed mutagenesis studies revealed that both stem structures and specific nucleotide sequence within the two loops are important for p58 binding. Mutations that disrupted stem structures abolished protein binding, while the compensatory mutations restored its binding. This region also contains partial sequence similarity to the reported consensus binding sequence for polypyrimidine tract-binding protein (PTB) (a 57-kDa protein). The UV-cross-linked protein could be immunoprecipitated with the anti-PTB antibody, and the recombinant PTB bound to the HCV 3'-UTR with the same binding specificity as p58, establishing that this protein is PTB. However, the reported PTB-binding sequence was not sufficient, but rather the entire stem-loops 2 and 3 were required, for PTB binding; thus, its binding specificity is significantly different from the reported PTB-binding sequence requirement. This protein was detected in both the nuclei and cytoplasm of most mammalian cell lines tested and human primary hepatocytes. PTB may participate in the regulation of HCV RNA synthesis or translation.

Citing Articles

Conformational dynamics of the hepatitis C virus 3'X RNA.

Sperstad P, Holmstrom E RNA. 2024; 30(9):1151-1163.

PMID: 38834242 PMC: 11331413. DOI: 10.1261/rna.079983.124.


Investigating the Human Host-ssRNA Virus Interaction Landscape Using the SMEAGOL Toolbox.

Lal A, Galvao Ferrarini M, Gruber A Viruses. 2022; 14(7).

PMID: 35891416 PMC: 9317827. DOI: 10.3390/v14071436.


Epidemiology, risk factors, and pathogenesis associated with a superbug: A comprehensive literature review on hepatitis C virus infection.

Tariq M, Shoukat A, Akbar S, Hameed S, Naqvi M, Azher A SAGE Open Med. 2022; 10:20503121221105957.

PMID: 35795865 PMC: 9252020. DOI: 10.1177/20503121221105957.


The low-resolution structural models of hepatitis C virus RNA subdomain 5BSL3.2 and its distal complex with domain 3'X point to conserved regulatory mechanisms within the Flaviviridae family.

Castillo-Martinez J, Fan L, Szewczyk M, Wang Y, Gallego J Nucleic Acids Res. 2022; 50(4):2287-2301.

PMID: 35137150 PMC: 8887478. DOI: 10.1093/nar/gkac061.


The Role of the RNA-RNA Interactome in the Hepatitis C Virus Life Cycle.

Romero-Lopez C, Berzal-Herranz A Int J Mol Sci. 2020; 21(4).

PMID: 32098260 PMC: 7073135. DOI: 10.3390/ijms21041479.


References
1.
SANGER F, Nicklen S, Coulson A . DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977; 74(12):5463-7. PMC: 431765. DOI: 10.1073/pnas.74.12.5463. View

2.
Zuker M, Stiegler P . Optimal computer folding of large RNA sequences using thermodynamics and auxiliary information. Nucleic Acids Res. 1981; 9(1):133-48. PMC: 326673. DOI: 10.1093/nar/9.1.133. View

3.
Dignam J, Lebovitz R, Roeder R . Accurate transcription initiation by RNA polymerase II in a soluble extract from isolated mammalian nuclei. Nucleic Acids Res. 1983; 11(5):1475-89. PMC: 325809. DOI: 10.1093/nar/11.5.1475. View

4.
Rice C, Lenches E, Eddy S, Shin S, Sheets R, Strauss J . Nucleotide sequence of yellow fever virus: implications for flavivirus gene expression and evolution. Science. 1985; 229(4715):726-33. DOI: 10.1126/science.4023707. View

5.
Choo Q, Kuo G, Weiner A, Overby L, Bradley D, Houghton M . Isolation of a cDNA clone derived from a blood-borne non-A, non-B viral hepatitis genome. Science. 1989; 244(4902):359-62. DOI: 10.1126/science.2523562. View