Oliveira Ana M M, Abel Ted, Brindle Paul K, Wood Marcelo A
Department of Biology, University of Pennsylvania, Philadelphia, PA, USA.
Behav Neurosci. 2006 Jun;120(3):724-9. doi: 10.1037/0735-7044.120.3.724.
Cyclic adenosine monophosphate response element binding protein (CREB) binding protein (CBP) and E1A binding protein (p300) are highly homologous transcriptional coactivators with histone acetyltransferase activity. Although CBP and p300 have unique functions in vivo during embryogenesis and hematopoiesis, their functions within the nervous system remain poorly understood. The authors demonstrate that these coactivators have differential roles in motor skill learning. Mice with a mutation in the CREB-binding (KIX) domain of CBP exhibited motor learning deficits. However, mice with the analogous mutation in the KIX domain of p300 showed normal motor learning. Further, CREB knock-out mice exhibited a motor learning deficit similar to that of CBP-KIX mutant mice. These results suggest that the CREB-CBP interaction is more limiting or critical than the CREB-p300 interaction for motor skill learning. Thus, CBP and p300 are genetically distinct at the behavioral level.
环磷腺苷反应元件结合蛋白(CREB)结合蛋白(CBP)和E1A结合蛋白(p300)是具有组蛋白乙酰转移酶活性的高度同源的转录共激活因子。尽管CBP和p300在胚胎发育和造血过程中在体内具有独特功能,但它们在神经系统中的功能仍知之甚少。作者证明这些共激活因子在运动技能学习中具有不同作用。CBP的CREB结合(KIX)结构域发生突变的小鼠表现出运动学习缺陷。然而,p300的KIX结构域发生类似突变的小鼠运动学习正常。此外,CREB基因敲除小鼠表现出与CBP-KIX突变小鼠类似的运动学习缺陷。这些结果表明,对于运动技能学习,CREB-CBP相互作用比CREB-p300相互作用更具限制性或更为关键。因此,在行为水平上,CBP和p300在基因上是不同的。