Gossels J M, Lewis S E, Perrone-Bizzozero N I, Benowitz L I
Mailman Research Center, McLean Hospital, Belmont, Massachusetts.
J Neurosci Res. 1992 Sep;33(1):112-21. doi: 10.1002/jnr.490330114.
Regeneration of the goldfish optic nerve involves massive changes in the structure and pattern of macro-molecular synthesis in the retinal ganglion cells. To explore the mechanisms that underlie these events, we investigated the changes in chromatin proteins during the course of regeneration. Three major retinal chromatin proteins, two with apparent molecular weights of 58 kDa (C1 and C2) and one at 51 kDa (C3), all having isoelectric points around 5.5, showed a fourfold increase in their synthesis and/or accumulation by 14 days of regeneration. Synthesis of C1 and C3 decreased by day 32, the time at which the axons have grown back to the optic tectum and have formed many of their synapses; synthesis of C2 remained high through day 32. All three proteins bound to DNA-cellulose and required high salt concentrations (0.2-0.5 M KCl) to be eluted. C1 and C2 had similar proteolytic digestion patterns and reacted with monoclonal antibodies that recognize the goldfish intermediate filament proteins of the ON complex. The proteins identified here could be involved in structural alterations in the chromatin, or might serve as transcription factors to regulate gene expression during nerve regeneration.
金鱼视神经的再生涉及视网膜神经节细胞中大分子合成的结构和模式的巨大变化。为了探究这些事件背后的机制,我们研究了再生过程中染色质蛋白的变化。三种主要的视网膜染色质蛋白,两种表观分子量为58 kDa(C1和C2),一种为51 kDa(C3),它们的等电点均在5.5左右,到再生14天时,其合成和/或积累增加了四倍。到第32天,轴突已长回到视顶盖并形成了许多突触,此时C1和C3的合成减少;C2的合成在第32天一直保持高水平。所有这三种蛋白都与DNA纤维素结合,需要高盐浓度(0.2 - 0.5 M KCl)才能洗脱。C1和C2具有相似的蛋白水解消化模式,并与识别ON复合体金鱼中间丝蛋白的单克隆抗体发生反应。这里鉴定出的蛋白可能参与染色质的结构改变,或者可能作为转录因子在神经再生过程中调节基因表达。