Cargando…

A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter

INTRODUCTION: While most transcripts arising from the human T Cell Receptor locus reflect fully rearranged genes, several germline transcripts have been identified. We describe a new germline transcript arising from the human TCRB locus. METHODS: cDNA sequencing, promoter, and gene expression analys...

Descripción completa

Detalles Bibliográficos
Autores principales: Lethé, Bernard, Snauwaert, Sylvia, Bricard, Orian, Schröder, David, Gomard, Tiphanie, Hames, Gérald, Muller, Catherine, Lurquin, Christophe, Gauthy, Emilie, Essaghir, Ahmed, Vandekerckhove, Bart, Coulie, Pierre G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569374/
https://www.ncbi.nlm.nih.gov/pubmed/28508570
http://dx.doi.org/10.1002/iid3.172
_version_ 1783258977200504832
author Lethé, Bernard
Snauwaert, Sylvia
Bricard, Orian
Schröder, David
Gomard, Tiphanie
Hames, Gérald
Muller, Catherine
Lurquin, Christophe
Gauthy, Emilie
Essaghir, Ahmed
Vandekerckhove, Bart
Coulie, Pierre G.
author_facet Lethé, Bernard
Snauwaert, Sylvia
Bricard, Orian
Schröder, David
Gomard, Tiphanie
Hames, Gérald
Muller, Catherine
Lurquin, Christophe
Gauthy, Emilie
Essaghir, Ahmed
Vandekerckhove, Bart
Coulie, Pierre G.
author_sort Lethé, Bernard
collection PubMed
description INTRODUCTION: While most transcripts arising from the human T Cell Receptor locus reflect fully rearranged genes, several germline transcripts have been identified. We describe a new germline transcript arising from the human TCRB locus. METHODS: cDNA sequencing, promoter, and gene expression analyses were used to characterize the new transcript. RESULTS: The new germline transcript encoded by the human TCRB locus consists of a new exon of 103 bp, which we named TRBX1 (X1), spliced with the first exon of gene segments Cß1 or Cß2. X1 is located upstream of gene segment Dß1 and is therefore deleted from a V‐DJ rearranged TCRB locus. The X1‐Cß transcripts do not appear to code for a protein. We define their transcription start and minimal promoter. These transcripts are found in populations of mature T lymphocytes from blood or tissues and in T cell clones with a monoallelic TCRB rearrangement. In immature thymocytes, they are already detectable in CD1a(−)CD34(+)CD4(−)CD8(−) cells, therefore before completion of the TCRB rearrangements. CONCLUSIONS: The X1 promoter appears to be the ortholog of the mouse pre‐Dß1 promoter (PDß1). Like PDß1, its activation is regulated by Eß in T cells and might facilitate the TCRB rearrangement process by contributing to the accessibility of the Dß1 locus.
format Online
Article
Text
id pubmed-5569374
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-55693742017-08-29 A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter Lethé, Bernard Snauwaert, Sylvia Bricard, Orian Schröder, David Gomard, Tiphanie Hames, Gérald Muller, Catherine Lurquin, Christophe Gauthy, Emilie Essaghir, Ahmed Vandekerckhove, Bart Coulie, Pierre G. Immun Inflamm Dis Original Research INTRODUCTION: While most transcripts arising from the human T Cell Receptor locus reflect fully rearranged genes, several germline transcripts have been identified. We describe a new germline transcript arising from the human TCRB locus. METHODS: cDNA sequencing, promoter, and gene expression analyses were used to characterize the new transcript. RESULTS: The new germline transcript encoded by the human TCRB locus consists of a new exon of 103 bp, which we named TRBX1 (X1), spliced with the first exon of gene segments Cß1 or Cß2. X1 is located upstream of gene segment Dß1 and is therefore deleted from a V‐DJ rearranged TCRB locus. The X1‐Cß transcripts do not appear to code for a protein. We define their transcription start and minimal promoter. These transcripts are found in populations of mature T lymphocytes from blood or tissues and in T cell clones with a monoallelic TCRB rearrangement. In immature thymocytes, they are already detectable in CD1a(−)CD34(+)CD4(−)CD8(−) cells, therefore before completion of the TCRB rearrangements. CONCLUSIONS: The X1 promoter appears to be the ortholog of the mouse pre‐Dß1 promoter (PDß1). Like PDß1, its activation is regulated by Eß in T cells and might facilitate the TCRB rearrangement process by contributing to the accessibility of the Dß1 locus. John Wiley and Sons Inc. 2017-05-15 /pmc/articles/PMC5569374/ /pubmed/28508570 http://dx.doi.org/10.1002/iid3.172 Text en © 2017 The Authors. Immunity, Inflammation and Disease Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Lethé, Bernard
Snauwaert, Sylvia
Bricard, Orian
Schröder, David
Gomard, Tiphanie
Hames, Gérald
Muller, Catherine
Lurquin, Christophe
Gauthy, Emilie
Essaghir, Ahmed
Vandekerckhove, Bart
Coulie, Pierre G.
A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title_full A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title_fullStr A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title_full_unstemmed A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title_short A new transcript in the TCRB locus unveils the human ortholog of the mouse pre‐Dß1 promoter
title_sort new transcript in the tcrb locus unveils the human ortholog of the mouse pre‐dß1 promoter
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5569374/
https://www.ncbi.nlm.nih.gov/pubmed/28508570
http://dx.doi.org/10.1002/iid3.172
work_keys_str_mv AT lethebernard anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT snauwaertsylvia anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT bricardorian anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT schroderdavid anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT gomardtiphanie anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT hamesgerald anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT mullercatherine anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT lurquinchristophe anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT gauthyemilie anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT essaghirahmed anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT vandekerckhovebart anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT couliepierreg anewtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT lethebernard newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT snauwaertsylvia newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT bricardorian newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT schroderdavid newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT gomardtiphanie newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT hamesgerald newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT mullercatherine newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT lurquinchristophe newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT gauthyemilie newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT essaghirahmed newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT vandekerckhovebart newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter
AT couliepierreg newtranscriptinthetcrblocusunveilsthehumanorthologofthemousepredß1promoter