Cargando…

FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia

RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from 19q13) that mapped upstream of the SLC7A10 locus. Reverse transcription-polymerase chain reaction together with Sanger seque...

Descripción completa

Detalles Bibliográficos
Autores principales: Panagopoulos, Ioannis, Gorunova, Ludmila, Torkildsen, Synne, Tierens, Anne, Heim, Sverre, Micci, Francesca
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403202/
https://www.ncbi.nlm.nih.gov/pubmed/28454383
http://dx.doi.org/10.3892/ol.2017.5705
_version_ 1783231387014266880
author Panagopoulos, Ioannis
Gorunova, Ludmila
Torkildsen, Synne
Tierens, Anne
Heim, Sverre
Micci, Francesca
author_facet Panagopoulos, Ioannis
Gorunova, Ludmila
Torkildsen, Synne
Tierens, Anne
Heim, Sverre
Micci, Francesca
author_sort Panagopoulos, Ioannis
collection PubMed
description RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from 19q13) that mapped upstream of the SLC7A10 locus. Reverse transcription-polymerase chain reaction together with Sanger sequencing verified the presence of this fusion transcript. The FAM53B fusion transcript is not expected to produce any chimeric protein. However, it may code for a truncated FAM53B protein consisting of the first 302 amino acids of FAM53B together with amino acids from the 19q13 sequence. Functionally, the truncated FAM53B would be similar to the protein encoded by the FAM53B sequence with accession no. BC031654.1 (FAM53B protein accession no. AAH31654.1). Furthermore, the truncated protein contains the entire conserved domain of the FAM53 protein family. The chromosome aberration t(10;19)(q26;q13) detected in this study was previously reported in a single case of ALL, in which it was also the sole karyotypic change. Both patients entered complete hematological and cytogenetic remission following treatment.
format Online
Article
Text
id pubmed-5403202
institution National Center for Biotechnology Information
language English
publishDate 2017
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-54032022017-04-27 FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia Panagopoulos, Ioannis Gorunova, Ludmila Torkildsen, Synne Tierens, Anne Heim, Sverre Micci, Francesca Oncol Lett Articles RNA-sequencing of the patient's bone marrow detected fusion transcripts in which the coding sequence of the FAM53B gene (from 10q26) was fused to a genomic sequence (from 19q13) that mapped upstream of the SLC7A10 locus. Reverse transcription-polymerase chain reaction together with Sanger sequencing verified the presence of this fusion transcript. The FAM53B fusion transcript is not expected to produce any chimeric protein. However, it may code for a truncated FAM53B protein consisting of the first 302 amino acids of FAM53B together with amino acids from the 19q13 sequence. Functionally, the truncated FAM53B would be similar to the protein encoded by the FAM53B sequence with accession no. BC031654.1 (FAM53B protein accession no. AAH31654.1). Furthermore, the truncated protein contains the entire conserved domain of the FAM53 protein family. The chromosome aberration t(10;19)(q26;q13) detected in this study was previously reported in a single case of ALL, in which it was also the sole karyotypic change. Both patients entered complete hematological and cytogenetic remission following treatment. D.A. Spandidos 2017-04 2017-02-08 /pmc/articles/PMC5403202/ /pubmed/28454383 http://dx.doi.org/10.3892/ol.2017.5705 Text en Copyright: © Panagopoulos et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Panagopoulos, Ioannis
Gorunova, Ludmila
Torkildsen, Synne
Tierens, Anne
Heim, Sverre
Micci, Francesca
FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title_full FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title_fullStr FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title_full_unstemmed FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title_short FAM53B truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
title_sort fam53b truncation caused by t(10;19)(q26;q13) chromosome translocation in acute lymphoblastic leukemia
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5403202/
https://www.ncbi.nlm.nih.gov/pubmed/28454383
http://dx.doi.org/10.3892/ol.2017.5705
work_keys_str_mv AT panagopoulosioannis fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia
AT gorunovaludmila fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia
AT torkildsensynne fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia
AT tierensanne fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia
AT heimsverre fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia
AT miccifrancesca fam53btruncationcausedbyt1019q26q13chromosometranslocationinacutelymphoblasticleukemia