Cargando…
Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts
BACKGROUND: Ghrelin is a multifunctional peptide hormone expressed in a range of normal tissues and pathologies. It has been reported that the human ghrelin gene consists of five exons which span 5 kb of genomic DNA on chromosome 3 and includes a 20 bp non-coding first exon (20 bp exon 0). The avail...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2007
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014779/ https://www.ncbi.nlm.nih.gov/pubmed/17727735 http://dx.doi.org/10.1186/1471-2164-8-298 |
_version_ | 1782136566355853312 |
---|---|
author | Seim, Inge Collet, Chris Herington, Adrian C Chopin, Lisa K |
author_facet | Seim, Inge Collet, Chris Herington, Adrian C Chopin, Lisa K |
author_sort | Seim, Inge |
collection | PubMed |
description | BACKGROUND: Ghrelin is a multifunctional peptide hormone expressed in a range of normal tissues and pathologies. It has been reported that the human ghrelin gene consists of five exons which span 5 kb of genomic DNA on chromosome 3 and includes a 20 bp non-coding first exon (20 bp exon 0). The availability of bioinformatic tools enabling comparative analysis and the finalisation of the human genome prompted us to re-examine the genomic structure of the ghrelin locus. RESULTS: We have demonstrated the presence of an additional novel exon (exon -1) and 5' extensions to exon 0 and 1 using comparative in silico analysis and have demonstrated their existence experimentally using RT-PCR and 5' RACE. A revised exon-intron structure demonstrates that the human ghrelin gene spans 7.2 kb and consists of six rather than five exons. Several ghrelin gene-derived splice forms were detected in a range of human tissues and cell lines. We have demonstrated ghrelin gene-derived mRNA transcripts that do not code for ghrelin, but instead may encode the C-terminal region of full-length preproghrelin (C-ghrelin, which contains the coding region for obestatin) and a transcript encoding obestatin-only. Splice variants that differed in their 5' untranslated regions were also found, suggesting a role of these regions in the post-transcriptional regulation of preproghrelin translation. Finally, several natural antisense transcripts, termed ghrelinOS (ghrelin opposite strand) transcripts, were demonstrated via orientation-specific RT-PCR, 5' RACE and in silico analysis of ESTs and cloned amplicons. CONCLUSION: The sense and antisense alternative transcripts demonstrated in this study may function as non-coding regulatory RNA, or code for novel protein isoforms. This is the first demonstration of putative obestatin and C-ghrelin specific transcripts and these findings suggest that these ghrelin gene-derived peptides may also be produced independently of preproghrelin. This study reveals several novel aspects of the ghrelin gene and suggests that the ghrelin locus is far more complex than previously recognised. |
format | Text |
id | pubmed-2014779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-20147792007-10-11 Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts Seim, Inge Collet, Chris Herington, Adrian C Chopin, Lisa K BMC Genomics Research Article BACKGROUND: Ghrelin is a multifunctional peptide hormone expressed in a range of normal tissues and pathologies. It has been reported that the human ghrelin gene consists of five exons which span 5 kb of genomic DNA on chromosome 3 and includes a 20 bp non-coding first exon (20 bp exon 0). The availability of bioinformatic tools enabling comparative analysis and the finalisation of the human genome prompted us to re-examine the genomic structure of the ghrelin locus. RESULTS: We have demonstrated the presence of an additional novel exon (exon -1) and 5' extensions to exon 0 and 1 using comparative in silico analysis and have demonstrated their existence experimentally using RT-PCR and 5' RACE. A revised exon-intron structure demonstrates that the human ghrelin gene spans 7.2 kb and consists of six rather than five exons. Several ghrelin gene-derived splice forms were detected in a range of human tissues and cell lines. We have demonstrated ghrelin gene-derived mRNA transcripts that do not code for ghrelin, but instead may encode the C-terminal region of full-length preproghrelin (C-ghrelin, which contains the coding region for obestatin) and a transcript encoding obestatin-only. Splice variants that differed in their 5' untranslated regions were also found, suggesting a role of these regions in the post-transcriptional regulation of preproghrelin translation. Finally, several natural antisense transcripts, termed ghrelinOS (ghrelin opposite strand) transcripts, were demonstrated via orientation-specific RT-PCR, 5' RACE and in silico analysis of ESTs and cloned amplicons. CONCLUSION: The sense and antisense alternative transcripts demonstrated in this study may function as non-coding regulatory RNA, or code for novel protein isoforms. This is the first demonstration of putative obestatin and C-ghrelin specific transcripts and these findings suggest that these ghrelin gene-derived peptides may also be produced independently of preproghrelin. This study reveals several novel aspects of the ghrelin gene and suggests that the ghrelin locus is far more complex than previously recognised. BioMed Central 2007-08-30 /pmc/articles/PMC2014779/ /pubmed/17727735 http://dx.doi.org/10.1186/1471-2164-8-298 Text en Copyright © 2007 Seim et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Seim, Inge Collet, Chris Herington, Adrian C Chopin, Lisa K Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title | Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title_full | Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title_fullStr | Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title_full_unstemmed | Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title_short | Revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
title_sort | revised genomic structure of the human ghrelin gene and identification of novel exons, alternative splice variants and natural antisense transcripts |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2014779/ https://www.ncbi.nlm.nih.gov/pubmed/17727735 http://dx.doi.org/10.1186/1471-2164-8-298 |
work_keys_str_mv | AT seiminge revisedgenomicstructureofthehumanghrelingeneandidentificationofnovelexonsalternativesplicevariantsandnaturalantisensetranscripts AT colletchris revisedgenomicstructureofthehumanghrelingeneandidentificationofnovelexonsalternativesplicevariantsandnaturalantisensetranscripts AT heringtonadrianc revisedgenomicstructureofthehumanghrelingeneandidentificationofnovelexonsalternativesplicevariantsandnaturalantisensetranscripts AT chopinlisak revisedgenomicstructureofthehumanghrelingeneandidentificationofnovelexonsalternativesplicevariantsandnaturalantisensetranscripts |