Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene

<p>Abstract</p> <p>Background</p> <p>The understanding of cutaneous pigmentation biology is relevant from the biologic and clinical point of view. The binding of α-melanocortin and its specific receptor, on the plasma membrane of melanin synthesising cells, plays a cruc...

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Main Authors: Natali Pier, Picardo Mauro, Pascucci Barbara, Miccadei Stefania, Civitareale Donato
Format: Article
Language:English
Published: BMC 2008-11-01
Series:Journal of Experimental & Clinical Cancer Research
Online Access:http://www.jeccr.com/content/27/1/71
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author Natali Pier
Picardo Mauro
Pascucci Barbara
Miccadei Stefania
Civitareale Donato
author_facet Natali Pier
Picardo Mauro
Pascucci Barbara
Miccadei Stefania
Civitareale Donato
author_sort Natali Pier
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>The understanding of cutaneous pigmentation biology is relevant from the biologic and clinical point of view. The binding of α-melanocortin and its specific receptor, on the plasma membrane of melanin synthesising cells, plays a crucial role in melanins biosynthesis. Furthermore, loss of <it>MC1R </it>function is associated with an increased incidence of melanoma and non-melanoma skin cancer. The expression of the α-melanocortin receptor gene is highly controlled but, at the present, region responsible for tissue-specific activity of the gene promoter has not been identified.</p> <p>Methods</p> <p>We have cloned the genomic sequences upstream the human MC1R coding gene. A DNA fragment of 5 kilobases upstream the human MC1R encoding sequence was placed in front of a reporter gene and several deletion mutants of such fragment have been prepared. These constructs have been tested for the ability to drive the melanocyte-specific gene expression of the reporter gene using transfection experiments in melanocyte and non-melanocyte cell lines. From these experiments we identified a DNA fragment with the ability to drive the gene transcription in a tissue-specific way and we used this small DNA fragment in DNA-protein interaction assays.</p> <p>Results</p> <p>We show that the 150 base pairs upstream the MC1R gene initiation codon are able to drive the melanocyte-specific gene transcription. Furthermore, we provide experimental evidences suggesting that on such minimal melanocyte-specific gene promoter can assemble tissue-specific complexes.</p> <p>Conclusion</p> <p>The present results strongly imply that the transcriptional regulation of the melanocyte-specific MC1R gene requires an internal promoter located in the 150 base pairs upstream the initiation codon.</p>
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spelling doaj.art-a121615d3d884dca985464ded6be30392022-12-22T01:08:20ZengBMCJournal of Experimental & Clinical Cancer Research1756-99662008-11-012717110.1186/1756-9966-27-71Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 geneNatali PierPicardo MauroPascucci BarbaraMiccadei StefaniaCivitareale Donato<p>Abstract</p> <p>Background</p> <p>The understanding of cutaneous pigmentation biology is relevant from the biologic and clinical point of view. The binding of α-melanocortin and its specific receptor, on the plasma membrane of melanin synthesising cells, plays a crucial role in melanins biosynthesis. Furthermore, loss of <it>MC1R </it>function is associated with an increased incidence of melanoma and non-melanoma skin cancer. The expression of the α-melanocortin receptor gene is highly controlled but, at the present, region responsible for tissue-specific activity of the gene promoter has not been identified.</p> <p>Methods</p> <p>We have cloned the genomic sequences upstream the human MC1R coding gene. A DNA fragment of 5 kilobases upstream the human MC1R encoding sequence was placed in front of a reporter gene and several deletion mutants of such fragment have been prepared. These constructs have been tested for the ability to drive the melanocyte-specific gene expression of the reporter gene using transfection experiments in melanocyte and non-melanocyte cell lines. From these experiments we identified a DNA fragment with the ability to drive the gene transcription in a tissue-specific way and we used this small DNA fragment in DNA-protein interaction assays.</p> <p>Results</p> <p>We show that the 150 base pairs upstream the MC1R gene initiation codon are able to drive the melanocyte-specific gene transcription. Furthermore, we provide experimental evidences suggesting that on such minimal melanocyte-specific gene promoter can assemble tissue-specific complexes.</p> <p>Conclusion</p> <p>The present results strongly imply that the transcriptional regulation of the melanocyte-specific MC1R gene requires an internal promoter located in the 150 base pairs upstream the initiation codon.</p>http://www.jeccr.com/content/27/1/71
spellingShingle Natali Pier
Picardo Mauro
Pascucci Barbara
Miccadei Stefania
Civitareale Donato
Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
Journal of Experimental & Clinical Cancer Research
title Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
title_full Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
title_fullStr Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
title_full_unstemmed Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
title_short Identification of the minimal melanocyte-specific promoter in the melanocortin receptor 1 gene
title_sort identification of the minimal melanocyte specific promoter in the melanocortin receptor 1 gene
url http://www.jeccr.com/content/27/1/71
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AT miccadeistefania identificationoftheminimalmelanocytespecificpromoterinthemelanocortinreceptor1gene
AT civitarealedonato identificationoftheminimalmelanocytespecificpromoterinthemelanocortinreceptor1gene