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一种与人类B1(CD20)抗原同源的、编码新的小鼠B淋巴细胞分化抗原的互补DNA的克隆,以及该基因在染色体19上的定位。

Cloning of a complementary DNA encoding a new mouse B lymphocyte differentiation antigen, homologous to the human B1 (CD20) antigen, and localization of the gene to chromosome 19.

作者信息

Tedder T F, Klejman G, Disteche C M, Adler D A, Schlossman S F, Saito H

机构信息

Division of Tumor Immunology, Dana-Farber Cancer Institute, Boston, MA 02115.

出版信息

J Immunol. 1988 Dec 15;141(12):4388-94.

PMID:2461992
Abstract

The human B1 (CD20) molecule is a differentiation Ag found only on the surface of B lymphocytes. This structurally unique phosphoprotein plays a role in the regulation of human B cell proliferation and differentiation. In order to determine whether this structure is also expressed by murine B cells, cDNA clones that encode the mouse equivalent of the B1 molecule were isolated. The longest murine cDNA clone isolated, pmB1-1, contained a 1.4-kb insert with an 873 base pair open reading frame that encodes a protein of 32 kDa. The predicted mouse B1 protein contains three hydrophobic domains that may span the membrane four times and shares a 73% amino acid sequence homology with the human B1 protein. The pmB1-1 cDNA probe was used to examine mB1 mRNA expression. Northern blot analysis indicated that pmB1-1 hybridized with two mRNA species of 2.3 and 3.0 kb that were expressed only in murine spleen lymphocytes, in B lineage cell lines representing mature B cells, and were weakly expressed in one of two plasmacytoma cell lines. pmB1-1 failed to hybridize with RNA isolated from murine T cell lines, thymus, and nonlymphoid tissues. Southern blot analysis indicated that mB1 was encoded by a single copy gene. In situ hybridization localized the mB1 gene to chromosome 19 band B, a region that also contains the genes that encode the Ly-1, Ly-10, and Ly-12 Ag. These results suggest that only B cells express this heretofore undescribed murine cell-surface protein that is structurally homologous with the membrane-embedded human B1 Ag.

摘要

人类B1(CD20)分子是一种仅在B淋巴细胞表面发现的分化抗原。这种结构独特的磷蛋白在人类B细胞增殖和分化的调节中发挥作用。为了确定这种结构是否也在鼠B细胞中表达,分离了编码小鼠等效B1分子的cDNA克隆。分离出的最长的鼠cDNA克隆pmB1-1包含一个1.4kb的插入片段,带有一个873个碱基对的开放阅读框,编码一个32kDa的蛋白质。预测的小鼠B1蛋白包含三个疏水结构域,可能跨膜四次,与人B1蛋白的氨基酸序列同源性为73%。使用pmB1-1 cDNA探针检测mB1 mRNA的表达。Northern印迹分析表明,pmB1-1与2.3kb和3.0kb的两种mRNA杂交,这两种mRNA仅在鼠脾淋巴细胞、代表成熟B细胞的B系细胞系中表达,并且在两个浆细胞瘤细胞系之一中弱表达。pmB1-1未能与从鼠T细胞系、胸腺和非淋巴组织分离的RNA杂交。Southern印迹分析表明,mB1由单拷贝基因编码。原位杂交将mB1基因定位到19号染色体B带,该区域还包含编码Ly-1、Ly-10和Ly-12抗原的基因。这些结果表明,只有B细胞表达这种迄今为止未描述的鼠细胞表面蛋白,该蛋白在结构上与膜嵌入的人类B1抗原同源。

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