Shibahara S, Taguchi H, Muller R M, Shibata K, Cohen T, Tomita Y, Tagami H
Department of Applied Physiology and Molecular Biology, Tohoku University School of Medicine, Miyagi, Japan.
J Biol Chem. 1991 Aug 25;266(24):15895-901.
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.
位于小鼠棕色(b)位点的色素细胞特异性基因已被克隆和鉴定。尽管其确切功能仍有待阐明,但它的基因产物是黑色黑色素形成所必需的,而非棕色黑色素。因此,在本报告中我们暂时将其命名为b位点蛋白。b位点蛋白基因长约18千碱基对,由8个外显子和7个内含子组成。对其启动子区域的功能分析表明,核苷酸残基-38/154足以在黑色素瘤全细胞提取物中指导色素细胞特异性转录。另一方面,我们在HeLa全细胞提取物中未能检测到其转录本。与另一个色素细胞特异性基因酪氨酸酶基因的启动子区域进行序列比较,发现b位点蛋白基因的两个元件(-33/-24和18/28)在酪氨酸酶基因的等效位置也保守,表明这两个元件可能参与其色素细胞特异性转录。此外,我们从小鼠B16黑色素瘤细胞的cDNA文库中克隆了一个编码b位点蛋白异构体的cDNA,pMT3。对pMT3的序列分析显示缺失103个碱基对,这对应于b位点蛋白基因外显子8的5'端,表明pMT3代表通过可变剪接产生的一种mRNA种类。由于这种缺失改变了阅读框并消除了b位点蛋白的跨膜结构域,pMT3型mRNA可能编码一种可溶性异构体。这种由553个氨基酸组成的异构体仅在其羧基末端不同,比b位点蛋白大16个氨基酸。通过瞬时表达分析,我们证实这种异构体能够与抗b位点蛋白单克隆抗体TMH-1反应,表明b位点蛋白异构体可能在色素沉着中具有某种功能。