Willecke K, Hennemann H, Dahl E, Jungbluth S, Heynkes R
Institut für Genetik (Abt. Molekulargenetik) Universität, Bonn/Bundersrepublik Deutschland.
Eur J Cell Biol. 1991 Oct;56(1):1-7.
The multigene family of connexins is larger than previously anticipated. Ten different connexin homologous sequences have been characterized in the mouse genome, five of which are probably the mouse analogues of the known rat connexins26, -31, -32, -43, and -46. Since the additional 5 sequences have been isolated as cDNAs or hybridize specifically to distinct mRNA species, they most likely represent functional connexin genes. Since seven of the genomic connexin sequences have been shown to contain no intron in the coding sequence, this may apply to all mammalian connexin genes. Some of the structural features based on amino acid sequences deduced from cDNA or genomic sequences and the RNA expression pattern of the new connexins are compared with previously described connexins. The structural diversity of the connexin genes suggests that they fulfill different functions coordinated with, and perhaps required for, different programs of cellular differentiation.
连接蛋白的多基因家族比之前预期的要大。在小鼠基因组中已鉴定出10种不同的连接蛋白同源序列,其中5种可能是已知大鼠连接蛋白26、-31、-32、-43和-46的小鼠类似物。由于另外5个序列已作为cDNA分离出来,或与不同的mRNA种类特异性杂交,它们很可能代表功能性连接蛋白基因。由于已证明7个基因组连接蛋白序列在编码序列中不含内含子,这可能适用于所有哺乳动物连接蛋白基因。将根据cDNA或基因组序列推导的氨基酸序列以及新连接蛋白的RNA表达模式得出的一些结构特征,与之前描述的连接蛋白进行了比较。连接蛋白基因的结构多样性表明,它们履行着与不同细胞分化程序相协调、或许也是这些程序所必需的不同功能。