Bartsch D, Casadio A, Karl K A, Serodio P, Kandel E R
Center for Neurobiology and Behavior, College of Physicians and Surgeons of Columbia University and New York State Psychiatric Institute, New York 10032, USA.
Cell. 1998 Oct 16;95(2):211-23. doi: 10.1016/s0092-8674(00)81752-3.
Although CREB seems to be important for memory formation, it is not known which of the isoforms of CREB, CREM, or ATF1 are expressed in the neurons that undergo long-term synaptic changes and what roles they have in memory formation. We have found a single Aplysia CREB1 gene homologous to both mammalian CREB and CREM and have characterized in the sensory neurons that mediate gill-withdrawal reflex the expression and function of the three proteins that it encodes: CREB1a, CREB1b, and CREB1c. CREB1a is a transcriptional activator that is both necessary and, upon phosphorylation, sufficient for long-term facilitation. CREB1b is a repressor of long-term facilitation. Cytoplasmic CREB1c modulates both the short- and long-term facilitation. Thus, in the sensory neurons, CREB1 encodes a critical regulatory unit converting short- to long-term synaptic changes.
尽管CREB似乎对记忆形成很重要,但尚不清楚CREB、CREM或ATF1的哪些亚型在经历长期突触变化的神经元中表达,以及它们在记忆形成中发挥什么作用。我们发现了一个与哺乳动物CREB和CREM同源的单一海兔CREB1基因,并在介导鳃收缩反射的感觉神经元中对其编码的三种蛋白质CREB1a、CREB1b和CREB1c的表达和功能进行了表征。CREB1a是一种转录激活因子,对长期易化作用既是必需的,磷酸化后也是充分的。CREB1b是长期易化作用的抑制因子。细胞质中的CREB1c调节短期和长期易化作用。因此,在感觉神经元中,CREB1编码一个关键的调节单元,将短期突触变化转化为长期突触变化。