Hisatomi Hisashi, Ohyashiki Kazuma, Ohyashiki Junko H, Nagao Kumi, Kanamaru Taichi, Hirata Hiroyuki, Hibi Nozomu, Tsukada Yutaka
Center for Molecular Biology and Cytogenetics, SRL Inc., 5-6-50 Shin-machi Hino, Tokyo, Japan.
Neoplasia. 2003 May-Jun;5(3):193-7. doi: 10.1016/S1476-5586(03)80051-9.
The human telomerase reverse transcriptase (hTERT) is an essential component of the holoenzyme complex that adds telomeric repeats to the ends of chromosomes. The hTERT transcript has been shown to have two deletion type alternative splicing sites. One deletion site induces the alpha-deletion variant, lacking 36 bp from exon 6, and the other induces the beta-deletion variant, lacking 182 bp from exons 7 and 8. Here, we identified a novel deletion variant of the hTERT transcript in hepatocellular carcinoma cell lines. The deleted transcript was characterized by an in-frame deletion of 189 bp, spanning nucleotides 2710 to 2898, corresponding to the complete loss of exon 11 (gamma-deletion). The region lacking in the gamma-deletion lies within RT motifs D and E, suggesting that it is missing conserved residues from the catalytic core of the protein. Both gamma- and alpha-deletion variants were occasionally detected, but the beta-deletion variant was frequently observed. Our results may provide important information for more detailed studies on the regulation of telomerase activity.
人端粒酶逆转录酶(hTERT)是全酶复合物的一个重要组成部分,该复合物可将端粒重复序列添加到染色体末端。hTERT转录本已被证明有两个缺失型可变剪接位点。一个缺失位点诱导α-缺失变体,缺失外显子6的36bp,另一个诱导β-缺失变体,缺失外显子7和8的182bp。在此,我们在肝癌细胞系中鉴定出一种新型的hTERT转录本缺失变体。缺失的转录本特征为189bp的框内缺失,跨越核苷酸2710至2898,对应于外显子11的完全缺失(γ-缺失)。γ-缺失所缺少的区域位于逆转录酶基序D和E内,这表明它缺失了该蛋白质催化核心的保守残基。γ-和α-缺失变体偶尔会被检测到,但β-缺失变体经常被观察到。我们的结果可能为更详细地研究端粒酶活性调控提供重要信息。