Okamoto T, Darbouy M, Brouillet A, Lahuna O, Chobert M N, Laperche Y
INSERM U.99, Hôpital Henri Mondor, Creteil, France.
Biochemistry. 1994 Sep 27;33(38):11536-43. doi: 10.1021/bi00204a016.
In the small intestine and in HTC hepatoma cells, the gamma-glutamyl transpeptidase (GGT) single-copy gene is transcribed into a 2.5 kb and a 2.2 kb mRNA. Cloning of the GGT cDNA sequences from HTC cells demonstrates that the 2.5 kb mRNA (mRNA(IV-1)) differs from the other rat GGT transcripts by a 371-base unique leader sequence which maps in the gene as 2 separate exons upstream of the 3 promoters which have been previously characterized. We established that the transcription of these two mRNAs is initiated on a new promoter (promoter IV) and occurs in the small intestine, in the epididymis, and in some hepatoma cells. The primary transcript initiated on GGT promoter IV is then alternatively spliced into the 2.5 kb mRNA(IV-1) or the 2.2 kb mRNA(IV-2) which is shorter in its 5'-untranslated sequence. The rat GGT gene exhibits a complex transcriptional organization leading to the transcription of five mRNAs from four independent promoters in a tissue-specific manner. The expression of the GGT promoter IV in the HTC hepatoma cells as well as in the small intestine could reveal that the HTC-transformed cells originate from liver precursor cells which still have the capacity to evolve toward different lineages. Thus, the GGT promoter IV will be valuable to isolate factors involved in the differentiation and carcinogenic processes.
在小肠和HTC肝癌细胞中,γ-谷氨酰转肽酶(GGT)单拷贝基因转录生成2.5 kb和2.2 kb的mRNA。从HTC细胞克隆GGT cDNA序列表明,2.5 kb的mRNA(mRNA(IV-1))与其他大鼠GGT转录本的不同之处在于有一个371个碱基的独特前导序列,该序列在基因中定位为位于先前已鉴定的3个启动子上游的2个独立外显子。我们确定这两种mRNA的转录起始于一个新的启动子(启动子IV),并发生在小肠、附睾和一些肝癌细胞中。在GGT启动子IV上起始的初级转录本随后被选择性剪接成2.5 kb的mRNA(IV-1)或5'-非翻译序列较短的2.2 kb的mRNA(IV-2)。大鼠GGT基因表现出复杂的转录组织,导致从四个独立启动子以组织特异性方式转录生成五种mRNA。GGT启动子IV在HTC肝癌细胞以及小肠中的表达可能表明,HTC转化细胞起源于仍有能力向不同谱系分化的肝前体细胞。因此,GGT启动子IV对于分离参与分化和致癌过程的因子将具有重要价值。