Literature DB >> 1908461

Structural organization of the pigment cell-specific gene located at the brown locus in mouse. Its promoter activity and alternatively spliced transcript.

S Shibahara1, H Taguchi, R M Muller, K Shibata, T Cohen, Y Tomita, H Tagami.   

Abstract

The pigment cell-specific gene, located at the brown (b) locus in mouse, has been cloned and characterized. Its gene product is required for the formation of black melanin rather than brown, although its exact function remains to be elucidated. We thus tentatively named it b-locus protein in this report. The b-locus protein gene is about 18 kilobase pairs long and organized into 8 exons and 7 introns. Functional analysis of its promoter region suggests that the nucleotide residues -38/154 is sufficient to direct the pigment cell-specific transcription in melanoma whole cell extracts. On the other hand, we were unable to detect its transcripts in HeLa whole cell extracts. Sequence comparison with the promoter region of the tyrosinase gene, another pigment cell-specific gene, reveals that two elements of the b-locus protein gene (-33/-24 and 18/28) are also conserved in the tyrosinase gene at equivalent positions, suggesting that these two elements may be involved in their pigment cell-specific transcription. Furthermore, we have cloned a cDNA, pMT3, coding for an isoform of b-locus protein from a cDNA library of mouse B16 melanoma cells. Sequence analysis of pMT3 reveals a deletion of 103 base pairs, which corresponds to the 5'-end of the exon 8 of the b-locus protein gene, indicating that pMT3 represents a mRNA species generated by alternative splicing. Since this deletion changes the reading frame and eliminates the transmembrane domain of b-locus protein, the pMT3-type mRNA may code for a soluble isoform. Such an isoform, consisting of 553 amino acids, differs only in its carboxyl terminus and is larger than b-locus protein by 16 amino acids. Using transient expression assays, we confirmed that such an isoform is able to react with anti-b-locus protein monoclonal antibody, TMH-1, suggesting that a b-locus protein isoform may have some function in pigmentation.

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Year:  1991        PMID: 1908461

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  11 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1991-12-11       Impact factor: 16.971

2.  Unraveling the melanocyte.

Authors:  V J Hearing
Journal:  Am J Hum Genet       Date:  1993-01       Impact factor: 11.025

3.  Complete sequence and polymorphism study of the human TYRP1 gene encoding tyrosinase-related protein 1.

Authors:  N F Box; J R Wyeth; C J Mayne; L E O'Gorman; N G Martin; R A Sturm
Journal:  Mamm Genome       Date:  1998-01       Impact factor: 2.957

4.  The semidominant Mi(b) mutation identifies a role for the HLH domain in DNA binding in addition to its role in protein dimerization.

Authors:  E Steingrímsson; A Nii; D E Fisher; A R Ferré-D'Amaré; R J McCormick; L B Russell; S K Burley; J M Ward; N A Jenkins; N G Copeland
Journal:  EMBO J       Date:  1996-11-15       Impact factor: 11.598

5.  Microphthalmia-associated transcription factor as a regulator for melanocyte-specific transcription of the human tyrosinase gene.

Authors:  K Yasumoto; K Yokoyama; K Shibata; Y Tomita; S Shibahara
Journal:  Mol Cell Biol       Date:  1994-12       Impact factor: 4.272

6.  Melanocyte-specific gene expression: role of repression and identification of a melanocyte-specific factor, MSF.

Authors:  U Yavuzer; C R Goding
Journal:  Mol Cell Biol       Date:  1994-05       Impact factor: 4.272

7.  Positive and negative elements regulate a melanocyte-specific promoter.

Authors:  P Lowings; U Yavuzer; C R Goding
Journal:  Mol Cell Biol       Date:  1992-08       Impact factor: 4.272

8.  A murine monoclonal antibody, MoAb HMSA-5, against a melanosomal component highly expressed in early stages, and common to normal and neoplastic melanocytes.

Authors:  J E Der; W T Dixon; K Jimbow; T Horikoshi
Journal:  Br J Cancer       Date:  1993-01       Impact factor: 7.640

9.  In silico screening and molecular dynamics simulation of disease-associated nsSNP in TYRP1 gene and its structural consequences in OCA3.

Authors:  Balu Kamaraj; Rituraj Purohit
Journal:  Biomed Res Int       Date:  2013-06-19       Impact factor: 3.411

Review 10.  Mutational analysis of oculocutaneous albinism: a compact review.

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Journal:  Biomed Res Int       Date:  2014-06-29       Impact factor: 3.411

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