Gangi-Peterson L, Peterson S N, Shapiro L H, Golding A, Caricchio R, Cohen D I, Margulies D H, Cohen P L
Curriculum in Genetics and Molecular Biology, St Jude Children's Research Hospital, Memphis, TN 38105, USA.
Mol Immunol. 1998 Jan;35(1):55-63. doi: 10.1016/s0161-5890(98)00008-x.
We have identified a novel activation related B-cell gene (bca) through differential hybridization screening of a murine B cell cDNA library. The deduced amino acid sequence predicted a protein of 482 amino acids with strong sequence similarity to the SH2 and SH3 domains present within the non-catalytic regions of several protein tyrosine kinases. Northern analysis of RNA from several murine B-cell lines revealed a transcript of 1.8 kb, which was not detected in T-cell and non-lymphoid cell lines. bca was transcribed at low levels in resting spleen cells from a variety of normal mouse strains and was strongly expressed in kidney RNA. bca expression was markedly increased in RNA prepared from mitogen activated B cells, and in freshly isolated spleen and lymph node cells of MRL/lpr and NZB autoimmune strains. The unique sequence of bca, which bears no obvious similarity to any specific class of proteins containing SH2 and SH3 domains, suggests that this gene encodes a novel protein potentially involved in B-cell signal transduction.
我们通过对小鼠B细胞cDNA文库进行差异杂交筛选,鉴定出了一个新的与激活相关的B细胞基因(bca)。推导的氨基酸序列预测该蛋白有482个氨基酸,与几种蛋白酪氨酸激酶非催化区域中的SH2和SH3结构域有很强的序列相似性。对几种小鼠B细胞系的RNA进行Northern分析,发现有一个1.8kb的转录本,在T细胞和非淋巴细胞系中未检测到。bca在多种正常小鼠品系的静息脾细胞中低水平转录,在肾RNA中强烈表达。bca在丝裂原激活的B细胞制备的RNA中,以及在MRL/lpr和NZB自身免疫品系的新鲜分离的脾细胞和淋巴结细胞中表达明显增加。bca的独特序列与任何含有SH2和SH3结构域的特定蛋白类别没有明显相似性,这表明该基因编码一种可能参与B细胞信号转导的新蛋白。