Pearson-White S, Crittenden R
Department of Microbiology, Box 441, University of Virginia Medical Center, Charlottesville, VA 22908, USA.
Nucleic Acids Res. 1997 Jul 15;25(14):2930-7. doi: 10.1093/nar/25.14.2930.
The mouse Sno gene, a Ski proto-oncogene homolog, expresses two isoforms, SnoN and SnoN2 (also called sno -dE3), which differ from each other in a location downstream from the site of alternative splicing previously described in the human SNO gene. SnoN2 is missing a 138 nt coding segment present in mouse SnoN and human SNON . We have cloned and sequenced the human ortholog of mouse SnoN2 , the existence of which was predicted from conservation of the alternative splice donor site that produces the SnoN2 isoform. Mouse SnoN2 and SnoN are expressed throughout embryonic development, in neonatal muscle and in many adult tissues. SnoN2 is the major species in most tissues, but SnoN and SnoN2 are expressed at approximately equal levels in brain. In human tissues, SNON2 is the less abundantly expressed isoform. Expression of mouse SnoN and SnoN2 mRNAs is induced with immediate early kinetics upon serum stimulation of quiescent fibroblasts, even in the presence of the protein synthesis inhibitor cycloheximide, while Ski is not. Interestingly, although both isoforms of Sno are induced, SnoN2 induction is much higher than SnoN . These data are consistent with a role for Sno in the response to proliferation stimuli.
小鼠Sno基因是Ski原癌基因的同源物,表达两种异构体,即SnoN和SnoN2(也称为sno -dE3),它们在先前人类SNO基因中描述的可变剪接位点下游的位置上彼此不同。SnoN2缺失了小鼠SnoN和人类SNON中存在的一个138 nt的编码片段。我们已经克隆并测序了小鼠SnoN2的人类同源物,其存在是根据产生SnoN2异构体的可变剪接供体位点的保守性预测的。小鼠SnoN2和SnoN在整个胚胎发育过程、新生肌肉以及许多成年组织中均有表达。SnoN2是大多数组织中的主要类型,但SnoN和SnoN2在大脑中的表达水平大致相等。在人类组织中,SNON2是表达较少的异构体。在血清刺激静止的成纤维细胞时,即使存在蛋白质合成抑制剂环己酰亚胺,小鼠SnoN和SnoN2 mRNA的表达也会以早期快速动力学方式被诱导,而Ski则不会。有趣的是,尽管Sno的两种异构体均被诱导,但SnoN2的诱导程度远高于SnoN。这些数据与Sno在对增殖刺激的反应中所起的作用一致。