Long terminal repeat
Long terminal repeats (LTRs) are identical sequences of DNA that repeat hundreds or thousands of times found at either end of retrotransposons or proviral DNA formed by reverse transcription of retroviral RNA. They are used by viruses to insert their genetic material into the host genomes.
Transcription
The LTRs are partially transcribed into an RNA intermediate, followed by reverse transcription into complementary DNA (cDNA) and ultimately dsDNA (double-stranded DNA) with full LTRs. The LTRs then mediate integration of the retroviral DNA via an LTR specific integrase into another region of the host chromosome. The first LTR sequences were derived by A.P. Czernilofsky and J. Shine in 1977 and 1980.[1][2]
Retroviruses such as Human Immunodeficiency Virus (HIV) use this basic mechanism.
Dating retroviral insertions using LTRs
As 5' and 3' LTRs are identical upon insertion, the difference between paired LTRs can be used to estimate the age of ancient retroviral insertions. This method of dating is used by paleovirologists, though it fails to take into account confounding factors such as gene-conversion and homologous recombination.
HIV-1
The HIV-1 LTR is 634 bp[3] in length and, like other retroviral LTRs, is segmented into the U3, R, and U5 regions. U3 and U5 has been further subdivided according to transcription factor sites and their impact on LTR activity and viral gene expression. The multi-step process of reverse transcription results in the placement of two identical LTRs, each consisting of a U3, R, and U5 region, at either end of the proviral DNA. The ends of the LTRs subsequently participate in integration of the provirus into the host genome. Once the provirus has been integrated, the LTR on the 5′ end serves as the promoter for the entire retroviral genome, while the LTR at the 3′ end provides for nascent viral RNA polyadenylation and, in HIV-1, HIV-2, and SIV, encodes the accessory protein, Nef.[4]
All of the required signals for gene expression are found in the LTRs: Enhancer, promoter (can have both transcriptional enhancers or regulatory elements), transcription initiation (such as capping), transcription terminator and polyadenylation signal.[5]
In HIV-1, the 5'UTR region has been characterized according to functional and structural differences into several sub-regions:
- TAR, or trans-activation response element, plays a critical role in transcriptional activation via its interaction with viral proteins. It forms a highly stable stem–loop structure consisting of 26 base pairs with a bulge in its secondary structure that interfaces with the viral transcription activator protein Tat.[6]
- Poly A plays roles both in dimerization and genome packaging since it is necessary for cleavage and polyadenylation. It has been reported that sequences upstream (U3 region) and downstream (U5 region) are needed in order to make the cleavage process efficient.[7]
- PBS, or primer binding site, is 18 nucleotides long and has a specific sequence that binds to the tRNALys primer required for initiation of reverse transcription.[8]
- Psi (Ψ), or the Psi packaging element, is a unique motif involved in regulating the packaging of the viral genome into the capsid. It is composed of four stem-loop (SL) structures with a major splicing donor site embedded in the second SL.[9]
- DIS, or dimer initiation site, is a highly conserved RNA–RNA interacting sequence constituting the SL1 stem–loop in the Psi packaging element of many retroviruses. DIS is characterized by a conserved stem and palindromic loop that forms a kissing-loop complex between HIV-1 RNA genomes to dimerize them for encapsidation.[10]
The transcript begins, at the beginning of R, is capped, and proceeds through U5 and the rest of the provirus, usually terminating by the addition of a poly A tract just after the R sequence in the 3' LTR.
The finding that both HIV LTRs can function as transcriptional promoters is not surprising since both elements are apparently identical in nucleotide sequence. Instead, the 3' LTR acts in transcription termination and polyadenylation. However, it has been suggested that the transcriptional activity of the 5' LTR is far greater than that of the 3' LTR, a situation that is very similar to that of other retroviruses.[5]
During transcription of the human immunodeficiency virus type 1 provirus, polyadenylation signals present in the 5' long terminal repeat (LTR) are disregarded while the identical polyadenylation signals present in the 3'LTR are utilized efficiently. It has been suggested that transcribed sequences present within the HIV-1 LTR U3 region act in cis to enhance polyadenylation within the 3' LTR.[11]
See also
External links
- Long Terminal Repeat at the US National Library of Medicine Medical Subject Headings (MeSH)
References
- ↑ Shine, J.; Czernilofsky, A. P.; Friedrich, R.; Bishop, J. M.; Goodman, H. M. (1977). "Nucleotide sequence at the 5' terminus of the avian sarcoma virus genome". Proceedings of the National Academy of Sciences. 74 (4): 1473–7. doi:10.1073/pnas.74.4.1473. PMC 430805
. PMID 67601. - ↑ Czernilofsky, A.P.; Delorbe, W.; Swanstrom, R.; Varmus, H.E.; Bishop, J.M.; Tischer, E.; Goodman, H.M. (1980). "The nucleotide sequence of an untranslated but conserved domain at the 3′ end of the avian sarcoma virus genome". Nucleic Acids Research. 8 (13): 2967–84. doi:10.1093/nar/8.13.2967. PMC 324138. PMID 6253899.
- ↑ Human Retroviruses and AIDS, 1998.
- ↑ Krebs, Fred C.; Hogan, Tricia H.; Quiterio, Shane; Gartner, Suzanne; Wigdahl, Brian (2001). "Lentiviral LTR-directed Expression, Sequence Variation, and Disease Pathogenesis" (PDF). In Kuiken, C; Foley, B; B; Marx, P; McCutchan, F; Mellors, JW; Wolinsky, S; Korber, B. HIV Sequence Compendium 2001. Los Alamos, NM: Theoretical Biology and Biophysics Group, Los Alamos National Laboratory. pp. 29–70.
- 1 2 Klaver, B; Berkhout, B (1994). "Comparison of 5' and 3' long terminal repeat promoter function in human immunodeficiency virus". Journal of Virology. 68 (6): 3830–40. PMC 236888. PMID 8189520.
- ↑ Wu, Yuntao (2004). "HIV-1 gene expression: Lessons from provirus and non-integrated DNA". Retrovirology. 1: 13. doi:10.1186/1742-4690-1-13. PMC 449739. PMID 15219234.
- ↑ Valsamakis, A; Schek, N; Alwine, JC (1992). "Elements upstream of the AAUAAA within the human immunodeficiency virus polyadenylation signal are required for efficient polyadenylation in vitro". Molecular and Cellular Biology. 12 (9): 3699–705. PMC 360226. PMID 1508176.
- ↑ Goldschmidt, V.; Rigourd, M; Ehresmann, C; Le Grice, SF; Ehresmann, B; Marquet, R (2002). "Direct and Indirect Contributions of RNA Secondary Structure Elements to the Initiation of HIV-1 Reverse Transcription". Journal of Biological Chemistry. 277 (45): 43233–42. doi:10.1074/jbc.M205295200. PMID 12194974.
- ↑ Johnson, Silas F.; Telesnitsky, Alice (2010). Madhani, Hiten D, ed. "Retroviral RNA Dimerization and Packaging: The What, How, when, Where, and Why". PLoS Pathogens. 6 (10): e1001007. doi:10.1371/journal.ppat.1001007. PMC 2951377. PMID 20949075.
- ↑ Heng, Xiao; Kharytonchyk, Siarhei; Garcia, Eric L.; Lu, Kun; Divakaruni, Sai Sachin; Lacotti, Courtney; Edme, Kedy; Telesnitsky, Alice; Summers, Michael F. (2012). "Identification of a Minimal Region of the HIV-1 5′-Leader Required for RNA Dimerization, NC Binding, and Packaging". Journal of Molecular Biology. 417 (3): 224–39. doi:10.1016/j.jmb.2012.01.033. PMC 3296369. PMID 22306406.
- ↑ Brown, PH; Tiley, LS; Cullen, BR (1991). "Efficient polyadenylation within the human immunodeficiency virus type 1 long terminal repeat requires flanking U3-specific sequences". Journal of Virology. 65 (6): 3340–3. PMC 240993. PMID 1851882.