García J I, Zalba G, Detera-Wadleigh S D, de Miguel C
Departamento de Bioquímica, Universidad de Navarra, Pamplona, Spain.
Mamm Genome. 1996 Nov;7(11):810-4. doi: 10.1007/s003359900242.
Using a combination of screening, RACE, and RT-PCR, we have isolated a new rat brain cDNA, we refer to as rMNK2, that showed strong homology to known MAP-kinases. The deduced amino acid sequence of rMNK2 indicated that it is the rat homolog of human p63(mapk), showing 94.5% identity. rMNK2 showed 77% homology with rat ERK3 and its human homolog p97(mapk), and 43% homology with both rat genes rMNK1(ERK1) and ERK2, within the kinase domain. This suggest that rMNK2 and ERK3 belong to a separate subfamily within the rat MAP-kinase multigene family. The most interesting difference lies in subdomain VIII, where this new subfamily contain a SEG/SPR motif instead of the TEY/APE found in the ERK subfamily, the TPY/APE found in the JNK/SAPK subfamily or the TGY/APE found in the p38/RK subfamily. The human homologs of ERK3 and rMNK2 (p97(mapk) and p63(mapk)) also show this significant change. Expression of rMNK2 has been detected in brain and to a lesser extent in lung by reverse transcription/PCR (RT-PCR). In situ hybridization of rat brain slices demonstrated a restricted expression of rMNK2 in the choroid plexus and hippocampus. This is interesting because the human homolog p63(mapk) maps to 18q12-21, a region that might be implicated in manic-depressive illness.
通过结合筛选、RACE和RT-PCR技术,我们分离出了一种新的大鼠脑cDNA,我们将其命名为rMNK2,它与已知的丝裂原活化蛋白激酶(MAP激酶)具有高度同源性。rMNK2推导的氨基酸序列表明它是人类p63(mapk)的大鼠同源物,同一性为94.5%。在激酶结构域内,rMNK2与大鼠ERK3及其人类同源物p97(mapk)的同源性为77%,与大鼠基因rMNK1(ERK1)和ERK2的同源性均为43%。这表明rMNK2和ERK3属于大鼠MAP激酶多基因家族中的一个独立亚家族。最有趣的差异在于亚结构域VIII,这个新亚家族在该区域包含一个SEG/SPR基序,而不是ERK亚家族中的TEY/APE基序、JNK/SAPK亚家族中的TPY/APE基序或p38/RK亚家族中的TGY/APE基序。ERK3和rMNK2的人类同源物(p97(mapk)和p63(mapk))也显示出这种显著变化。通过逆转录/PCR(RT-PCR)检测到rMNK2在脑中表达,在肺中表达较少。大鼠脑切片的原位杂交显示rMNK2在脉络丛和海马中表达受限。这很有趣,因为人类同源物p63(mapk)定位于18q12 - 21,该区域可能与躁郁症有关。