Ruppert S, Cole T J, Boshart M, Schmid E, Schütz G
German Cancer Research Center, Institute of Cell and Tumor Biology, Heidelberg.
EMBO J. 1992 Apr;11(4):1503-12. doi: 10.1002/j.1460-2075.1992.tb05195.x.
We have characterized cDNA clones representing mouse CREB (cyclic AMP responsive element binding protein) mRNA isoforms. These include CREB delta and CREB alpha, of which the rat and human homologues have been previously identified. Both encode proteins with CRE-binding activity and identical transactivation potential. The additional CREB mRNA isoforms potentially encode CREB related proteins. From the structural organization of the mouse CREB gene we conclude that the multiple transcripts are generated by alternative splicing. Furthermore we show that specific CREB mRNA isoforms are expressed at a high level in the adult testis. Expression of these isoforms is induced after commencement of spermatogenesis. In situ hybridization suggests that this expression occurs predominantly in the primary spermatocytes. Comparison of the CREB gene with the recently isolated CREM (cAMP responsive element modulator) cDNAs illustrates that the two genes have arisen by gene duplication and have diverged to encode transcriptional activators and repressors of the cAMP signal transduction pathway.
我们已对代表小鼠CREB(环磷酸腺苷反应元件结合蛋白)mRNA异构体的cDNA克隆进行了特征分析。这些异构体包括CREBδ和CREBα,其大鼠和人类同源物此前已被鉴定。两者均编码具有CRE结合活性和相同反式激活潜能的蛋白质。额外的CREB mRNA异构体可能编码与CREB相关的蛋白质。从小鼠CREB基因的结构组织我们得出结论,多个转录本是由可变剪接产生的。此外,我们表明特定的CREB mRNA异构体在成年睾丸中高水平表达。这些异构体的表达在精子发生开始后被诱导。原位杂交表明这种表达主要发生在初级精母细胞中。将CREB基因与最近分离的CREM(环磷酸腺苷反应元件调节剂)cDNA进行比较表明,这两个基因是通过基因复制产生的,并且已经分化以编码环磷酸腺苷信号转导途径的转录激活剂和抑制剂。