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Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity
The luteinizing hormone beta subunit (LH-beta) gene plays a critical role in reproduction. In order to characterize and analyze the promoter region of LH-beta in sheep, a genomic library was constructed in phage lambda gt 10 and screened. A novel region of 1,224 bp upstream from the targeted LH-beta...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer International Publishing
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554545/ https://www.ncbi.nlm.nih.gov/pubmed/26355566 http://dx.doi.org/10.1186/s40064-015-1182-5 |
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author | Aherrahrou, Redouane Aherrahrou, Zouhair Erdmann, Jeanette Moumni, Mohieddine |
author_facet | Aherrahrou, Redouane Aherrahrou, Zouhair Erdmann, Jeanette Moumni, Mohieddine |
author_sort | Aherrahrou, Redouane |
collection | PubMed |
description | The luteinizing hormone beta subunit (LH-beta) gene plays a critical role in reproduction. In order to characterize and analyze the promoter region of LH-beta in sheep, a genomic library was constructed in phage lambda gt 10 and screened. A novel region of 1,224 bp upstream from the targeted LH-beta gene was identified. Blasting this sequence showed a perfect homology for the first 721 bp sequence with an upstream ovine LH-beta sequence in the database. However, the remaining 5′-503 bp showed no sequence matching. DNA from Moroccan breeds was isolated and the whole region was amplified and confirmed by sequencing. To further confirm the promoter activity of this region, an in vitro analysis using a luciferase assay was carried out. An increase in the promoter activity of the whole region was demonstrated compared to the empty vector. More interestingly, the unpublished region significantly enhanced the promoter activity compared to the known region alone. To predict putative transcription factor binding-sites (TFBSs), an in silico analysis was performed using the TFSEARCH program. The region features many TFBSs and contains two palindrome sequences of 17- and 18-bp. Taken together, a novel region was identified and confirmed in sheep which contained a promoter activity rich with binding sites for a putative regulatory element as shown in silico. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-015-1182-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4554545 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-45545452015-09-09 Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity Aherrahrou, Redouane Aherrahrou, Zouhair Erdmann, Jeanette Moumni, Mohieddine Springerplus Research The luteinizing hormone beta subunit (LH-beta) gene plays a critical role in reproduction. In order to characterize and analyze the promoter region of LH-beta in sheep, a genomic library was constructed in phage lambda gt 10 and screened. A novel region of 1,224 bp upstream from the targeted LH-beta gene was identified. Blasting this sequence showed a perfect homology for the first 721 bp sequence with an upstream ovine LH-beta sequence in the database. However, the remaining 5′-503 bp showed no sequence matching. DNA from Moroccan breeds was isolated and the whole region was amplified and confirmed by sequencing. To further confirm the promoter activity of this region, an in vitro analysis using a luciferase assay was carried out. An increase in the promoter activity of the whole region was demonstrated compared to the empty vector. More interestingly, the unpublished region significantly enhanced the promoter activity compared to the known region alone. To predict putative transcription factor binding-sites (TFBSs), an in silico analysis was performed using the TFSEARCH program. The region features many TFBSs and contains two palindrome sequences of 17- and 18-bp. Taken together, a novel region was identified and confirmed in sheep which contained a promoter activity rich with binding sites for a putative regulatory element as shown in silico. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40064-015-1182-5) contains supplementary material, which is available to authorized users. Springer International Publishing 2015-09-01 /pmc/articles/PMC4554545/ /pubmed/26355566 http://dx.doi.org/10.1186/s40064-015-1182-5 Text en © Aherrahrou et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Research Aherrahrou, Redouane Aherrahrou, Zouhair Erdmann, Jeanette Moumni, Mohieddine Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title_full | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title_fullStr | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title_full_unstemmed | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title_short | Identification of a novel ovine LH-beta promoter region, which dramatically enhances its promoter activity |
title_sort | identification of a novel ovine lh-beta promoter region, which dramatically enhances its promoter activity |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4554545/ https://www.ncbi.nlm.nih.gov/pubmed/26355566 http://dx.doi.org/10.1186/s40064-015-1182-5 |
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