Biopolym. Cell. 2013; 29(6):454-462.
Structure and Function of Biopolymers
Phylogenetic study on structural elements of HIV-1
poly(A) region. 1. PolyA and DSE hairpins
- Institute of Molecular Biology and Genetics, NAS of Ukraine
150, Akademika Zabolotnoho Str., Kyiv, Ukraine, 03680
Abstract
Genome of human immunodeficiency virus type 1 (HIV-1) is highly heterogeneous. The aim of this work was a phylogenetic study on structural elements of the HIV-1 poly(A) region, in particular polyA and DSE hairpins which compose a core poly(A) site. Methods. The secondary structure of the HIV-1 core poly(A) site has been predicted by the UNAFold program. Results. The structure of the polyA and DSE hairpins has been analysed in 1679 HIV-1 genomes of group M and 18 genomes of simian immunodeficiency virus SIVcpzPtt. We found 244 and 171 different sequences for the HIV-1 polyA and DSE hairpins, respectively. However 70 % of the HIV-1 isolates studied contain one of 7 variants of the polyA hairpin which occur with a frequency 5 % (main variants) and 79 % of the isolates contain one of 7 main variants of the DSE hairpin. We also revealed subtype and country specific mutations in these hairpins. We found that the SIV polyA hairpin most closely resembles that found in HIV-1 genomes of B/C subtypes. Conclusions. The results of our large-scale phylogenetic study support some structural models of the HIV-1 5' UTR, in particular the tertiary interaction between the polyA hairpin and the matrix region in HIV-1 gRNA. Possibly, the DSE hairpin appeared in the course of viral evolution of the HIV-1 group M. An exposure of the U/GU-rich element in the apical loop of DSE hairpin could significantly increase the efficiency of pre-mRNA polyadenylation in this HIV-1 group.
Keywords: HIV-1, SIVcpzPtt, poly(A) region, secondary structure, polyA hairpin, DSE hairpin
Full text: (PDF, in English)
Supplementary data
References
[1]
Zarudnaya M. I. mRNA polyadenylation. 1. 3'-end formation of vertebrates' mRNAs Biopolym. Cell 2001 17, N 2 P. 93–108.
[2]
Chan S., Choi E. A., Shi Y. Pre-mRNA 3'-end processing complex assembly and function Wiley Interdiscip. Rev. RNA 2011 2, N 3:321–335.
[3]
Zarudnaya M. I., Potyahaylo A. L., Kolomiets I. M., Hovorun D. M. Auxiliary elements of mammalian pre-mRNAs polyadenylation signals Biopolym. Cell 2002 18, N 6:500–517.
[4]
Valsamakis A., Zeichner S., Carswell S., Alwine J. C. The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation Proc. Natl Acad. Sci. USA 1991 88, N 6:2108–2112.
[5]
Berkhout B., Klaver B., Das A. T. A conserved hairpin structure predicted for the poly(A) signal of human and simian immunodeficiency viruses Virology 1995 207, N 1:276–281.
[6]
Klasens B. I., Thiesen M., Virtanen A., Berkhout B. The ability of the HIV-1 AAUAAA signal to bind polyadenylation factors is controlled by local RNA structure Nucleic Acids Res 1999 27, N 2:446–454.
[7]
Zarudnaya MI, Potyahaylo AL, Otenko VV, Kolomiets IN, Hovorun DM. The secondary structure of core poly(A) signal of human immunodeficiency virus pre-mRNA. Dopovidi Nats Akad Nauk Ukrainy. 2011;(4):170-6.
[8]
Paillart J. C., Skripkin E., Ehresmann B., Ehresmann C., Marquet R. In vitro evidence for a long range pseudoknot in the 5'untranslated and matrix coding regions of HIV-1 genomic RNA J. Biol. Chem 2002 277, N 8:5995–6004.
[9]
Abbink T. E., Berkhout B. A novel long distance base-pairing interaction in human immunodeficiency virus type 1 RNA occludes the Gag start codon J. Biol. Chem 2003 278, N 13 P. 11601–11611.
[10]
Ooms M., Cupac D., Abbink T. E., Huthoff H., Berkhout B. The availability of the primer activation signal (PAS) affects the efficiency of HIV-1 reverse transcription initiation Nucleic Acids Res 2007 35, N 5:1649–1659.
[11]
Markham N. R., Zuker M. UNAFold: software for nucleic acid folding and hybridization Methods Mol. Biol 2008 453 P. 3–31.
[12]
Yuan Y., Kerwood D. J., Paoletti A. C., Shubsda M. F., Borer P. N. Stem of SL1 RNA in HIV-1: structure and nucleocapsid protein binding for a 1 x 3 internal loop Biochemistry 2003 42, N 18:5259–5269.
[13]
Henriet S., Richer D., Bernacchi S., Decroly E., Vigne R., Ehresmann B., Ehresmann C., Paillart J. C., Marquet R. Cooperative and specific binding of Vif to the 5' region of HIV-1 genomic RNA J. Mol. Biol 2005 354, N 1:55–72.
[14]
Das A. T., Klaver B., Berkhout B. A hairpin structure in the R region of the human immunodeficiency virus type 1 RNA genome is instrumental in polyadenylation site selection J. Virol 1999 73, N 1:81–91.
[16]
Sharp P. M., Hahn B. H. Origins of HIV and the AIDS pandemic Cold Spring Harb. Perspect. Med 2011 1, N 1 a006841.
[17]
Zarudnaya M. I., Kolomiets I. M., Potyahaylo A. L., Hovorun D. M. Downstream elements of mammalian pre-mRNA polyadenylation signals: primary, secondary and higher-order structures Nucleic Acids Res 2003 31, N 5:1375–1386.
[18]
Chou Z.-F., Chen F., Wilusz J. Sequence and position requirements for uridylate-rich downstream elements of polyadenylation signals Nucleic Acids Res 1994 22, N 13:2525– 2531.