Sévigny G, Lemieux N, Steyaert A, Bibor-Hardy V
Institut du cancer de Montréal, Centre de recherche Louis-Charles Simard, Québec, Canada.
Genomics. 1996 Jan 1;31(1):107-10. doi: 10.1006/geno.1996.0015.
TRiC is a cytoplasmic chaperonin involved in actin and tubulin folding. It is formed by six to nine different but related proteins of 52 to 65 kDa arranged in two hetero-oligomeric rings. We have cloned the gene coding for the mouse TRiC-P5 subunit (also called CCT gamma) using a XbaI-DraIII fragment of the mTRiC5 cDNA. The mouse genome contains one TRiC5 gene and one TRiC5 pseudogene located on chromosomes 3F and 5B, respectively. The 2-kb transcript of TRiC5 is encoded by 14 exons distributed within 25 kb of genomic DNA. The largest exon is 312 bp and the smallest exon is 51 bp. We have used primer extension to demonstrate multiple transcription start points for the TRiC5 gene. This is consistent with the lack of any obvious TATA box upstream of the transcription start points.
TRiC是一种参与肌动蛋白和微管蛋白折叠的胞质伴侣蛋白。它由6至9种不同但相关的蛋白质组成,这些蛋白质分子量在52至65 kDa之间,排列成两个异源寡聚环。我们利用mTRiC5 cDNA的XbaI - DraIII片段克隆了编码小鼠TRiC - P5亚基(也称为CCTγ)的基因。小鼠基因组包含一个TRiC5基因和一个TRiC5假基因,分别位于3F和5B染色体上。TRiC5的2 kb转录本由分布在25 kb基因组DNA内的14个外显子编码。最大的外显子为312 bp,最小的外显子为51 bp。我们使用引物延伸法证明了TRiC5基因有多个转录起始点。这与转录起始点上游缺乏任何明显的TATA盒是一致的。