Erck C, MacLeod R A F, Wehland J
Department of Cell Biology, German Research Center of Biotechnology, Braunschweig, Germany.
Cytogenet Genome Res. 2003;101(1):47-53. doi: 10.1159/000073418.
Tubulin tyrosine ligase (TTL) is a cytosolic enzyme involved in the posttranslational modification of tubulin. In the assembled form microtubules are detyrosinated over time at the C-terminus of alpha-tubulin. After microtubular disassembly TTL restores tyrosine residues back to the detyrosinated tubulin leading to a cycle of detyrosination/tyrosination. Here we report the isolation of the human and mouse TTL cDNA. In comparison with other known TTL sequences, namely bovine, rat and porcine, we found that only porcine TTL deviates in length by having an insertion of two glutamate residues. In mouse and human TTL the genomic coding sequence is composed of seven exons with normal intron/exon boundaries. Using fluorescence in situ hybridization (FISH), we mapped the murine TTL gene to mouse chromosome 2 (MMU2). Human TTL has been located to chromosome 2q13 (HSA2q13). In addition, we found frequently truncated PCR products of hTTL transcripts with aberrant splicing in tumors.
微管蛋白酪氨酸连接酶(TTL)是一种参与微管蛋白翻译后修饰的胞质酶。在组装形式下,微管随着时间的推移在α-微管蛋白的C末端发生去酪氨酸化。微管解聚后,TTL将酪氨酸残基恢复到去酪氨酸化的微管蛋白上,导致去酪氨酸化/酪氨酸化循环。在此,我们报告了人和小鼠TTL cDNA的分离。与其他已知的TTL序列,即牛、大鼠和猪的序列相比,我们发现只有猪的TTL长度存在偏差,有两个谷氨酸残基的插入。在小鼠和人TTL中,基因组编码序列由七个外显子组成,具有正常的内含子/外显子边界。使用荧光原位杂交(FISH),我们将小鼠TTL基因定位到小鼠2号染色体(MMU2)。人TTL已定位到2号染色体q13区(HSA2q13)。此外,我们在肿瘤中经常发现hTTL转录本的截断PCR产物,伴有异常剪接。