HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated

<p>Abstract</p> <p>Background</p> <p>Antisense transcription in retroviruses has been suggested for both HIV-1 and HTLV-I, although the existence and coding potential of these transcripts remain controversial. Thorough characterization is required to demonstrate the exi...

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Main Authors: Marriott Susan J, Wattel Éric, Thête Julien, Paré Marie-Ève, Hivin Patrick, Arpin-André Charlotte, Audet Brigitte, Landry Sébastien, Cavanagh Marie-Hélène, Mesnard Jean-Michel, Barbeau Benoit
Format: Article
Language:English
Published: BMC 2006-03-01
Series:Retrovirology
Online Access:http://www.retrovirology.com/content/3/1/15
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author Marriott Susan J
Wattel Éric
Thête Julien
Paré Marie-Ève
Hivin Patrick
Arpin-André Charlotte
Audet Brigitte
Landry Sébastien
Cavanagh Marie-Hélène
Mesnard Jean-Michel
Barbeau Benoit
author_facet Marriott Susan J
Wattel Éric
Thête Julien
Paré Marie-Ève
Hivin Patrick
Arpin-André Charlotte
Audet Brigitte
Landry Sébastien
Cavanagh Marie-Hélène
Mesnard Jean-Michel
Barbeau Benoit
author_sort Marriott Susan J
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Antisense transcription in retroviruses has been suggested for both HIV-1 and HTLV-I, although the existence and coding potential of these transcripts remain controversial. Thorough characterization is required to demonstrate the existence of these transcripts and gain insight into their role in retrovirus biology.</p> <p>Results</p> <p>This report provides the first complete characterization of an antisense retroviral transcript that encodes the previously described HTLV-I HBZ protein. In this study, we show that HBZ-encoding transcripts initiate in the 3' long terminal repeat (LTR) at several positions and consist of two alternatively spliced variants (SP1 and SP2). Expression of the most abundant HBZ spliced variant (SP1) could be detected in different HTLV-I-infected cell lines and importantly in cellular clones isolated from HTLV-I-infected patients. Polyadenylation of HBZ RNA occurred at a distance of 1450 nucleotides downstream of the HBZ stop codon in close proximity of a typical polyA signal. We have also determined that translation mostly initiates from the first exon located in the 3' LTR and that the HBZ isoform produced from the SP1 spliced variant demonstrated inhibition of Tax and c-Jun-dependent transcriptional activation.</p> <p>Conclusion</p> <p>These results conclusively demonstrate the existence of antisense transcription in retroviruses, which likely plays a role in HTLV-I-associated pathogenesis through HBZ protein synthesis.</p>
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spelling doaj.art-6d5ed85416c7480dbe7d459130d62e3d2022-12-22T01:06:35ZengBMCRetrovirology1742-46902006-03-01311510.1186/1742-4690-3-15HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylatedMarriott Susan JWattel ÉricThête JulienParé Marie-ÈveHivin PatrickArpin-André CharlotteAudet BrigitteLandry SébastienCavanagh Marie-HélèneMesnard Jean-MichelBarbeau Benoit<p>Abstract</p> <p>Background</p> <p>Antisense transcription in retroviruses has been suggested for both HIV-1 and HTLV-I, although the existence and coding potential of these transcripts remain controversial. Thorough characterization is required to demonstrate the existence of these transcripts and gain insight into their role in retrovirus biology.</p> <p>Results</p> <p>This report provides the first complete characterization of an antisense retroviral transcript that encodes the previously described HTLV-I HBZ protein. In this study, we show that HBZ-encoding transcripts initiate in the 3' long terminal repeat (LTR) at several positions and consist of two alternatively spliced variants (SP1 and SP2). Expression of the most abundant HBZ spliced variant (SP1) could be detected in different HTLV-I-infected cell lines and importantly in cellular clones isolated from HTLV-I-infected patients. Polyadenylation of HBZ RNA occurred at a distance of 1450 nucleotides downstream of the HBZ stop codon in close proximity of a typical polyA signal. We have also determined that translation mostly initiates from the first exon located in the 3' LTR and that the HBZ isoform produced from the SP1 spliced variant demonstrated inhibition of Tax and c-Jun-dependent transcriptional activation.</p> <p>Conclusion</p> <p>These results conclusively demonstrate the existence of antisense transcription in retroviruses, which likely plays a role in HTLV-I-associated pathogenesis through HBZ protein synthesis.</p>http://www.retrovirology.com/content/3/1/15
spellingShingle Marriott Susan J
Wattel Éric
Thête Julien
Paré Marie-Ève
Hivin Patrick
Arpin-André Charlotte
Audet Brigitte
Landry Sébastien
Cavanagh Marie-Hélène
Mesnard Jean-Michel
Barbeau Benoit
HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
Retrovirology
title HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
title_full HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
title_fullStr HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
title_full_unstemmed HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
title_short HTLV-I antisense transcripts initiating in the 3'LTR are alternatively spliced and polyadenylated
title_sort htlv i antisense transcripts initiating in the 3 ltr are alternatively spliced and polyadenylated
url http://www.retrovirology.com/content/3/1/15
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