Hidaka K, Morisaki T, Byun S H, Hashido K, Toyama K, Mukai T
Department of Bioscience, National Cardiovascular Center Research Institute, Osaka, Japan.
Biochem Biophys Res Commun. 1995 Aug 15;213(2):555-60. doi: 10.1006/bbrc.1995.2167.
The MEF2 gene family encodes a MADS-box transcription factor which regulates expression of many muscle-specific genes. We examined the expression of the MEF2 genes in mouse embryonal carcinoma P19 cells before and after in vitro muscle differentiation induced by dimethyl sulfoxide (DMSO). At least three different MADS/MEF2 domains (MEF2A, 2B and 2D) were isolated from P19 cells with the MOPAC technique (mixed oligonucleotides primed amplification of cDNA). Although two of the MADS/MEF2 domain sequences were identical to those of human MEF2A and MEF2D, another domain sequence was similar but not identical to that of human MEF2B. While the transcription of MEF2A and MEF2D was up-regulated during differentiation of P19 cells, the MEF2B homologue was abundantly transcribed in undifferentiated P19, F9 and ES cells and down-regulated in adult heart, skeletal muscle or brain, suggesting that the murine MEF2B homologue might have a function distinct from other members of the MEF2 gene family in embryogenesis and development.
MEF2基因家族编码一种MADS盒转录因子,该因子调控许多肌肉特异性基因的表达。我们检测了在二甲基亚砜(DMSO)诱导的体外肌肉分化前后,小鼠胚胎癌P19细胞中MEF2基因的表达情况。利用MOPAC技术(混合寡核苷酸引发的cDNA扩增)从P19细胞中分离出至少三种不同的MADS/MEF2结构域(MEF2A、2B和2D)。虽然其中两个MADS/MEF2结构域序列与人MEF2A和MEF2D的序列相同,但另一个结构域序列与人MEF2B的序列相似但不同。在P19细胞分化过程中,MEF2A和MEF2D的转录上调,而MEF2B同源物在未分化的P19、F9和ES细胞中大量转录,在成年心脏、骨骼肌或大脑中下调,这表明小鼠MEF2B同源物在胚胎发生和发育过程中可能具有与MEF2基因家族其他成员不同的功能。