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参与甲状腺癌的人类TFG基因的特征分析与染色体定位

Characterization and chromosomal mapping of the human TFG gene involved in thyroid carcinoma.

作者信息

Mencinger M, Panagopoulos I, Andreasson P, Lassen C, Mitelman F, Aman P

机构信息

Department of Clinical Genetics, University Hospital of Lund, Sweden.

出版信息

Genomics. 1997 May 1;41(3):327-31. doi: 10.1006/geno.1997.4625.

Abstract

Homology searches in the Expressed Sequence Tag Database were performed using SPYGQ-rich regions as query sequences to find genes encoding protein regions similar to the N-terminal parts of the sarcoma-associated EWS and FUS proteins. Clone 22911 (T74973), encoding a SPYGQ-rich region in its 5' end, and several other clones that overlapped 22911 were selected. The combined data made it possible to assemble a full-length cDNA sequence. This cDNA sequence is 1677 bp, containing an initiation codon ATG, an open reading frame of 400 amino acids, a poly(A) signal, and a poly(A) tail. We found 100% identity between the 5' part of the consensus sequence and the 598-bp-long sequence named TFG. The TFG sequence is fused to the 3' end of NTRK1, generating the TRK-T3 fusion transcript found in papillary thyroid carcinoma. The cDNA therefore represents the full-length transcript of the TFG gene. TFG was localized to 3q11-q12 by fluorescence in situ hybridization. The 3' and the 5' ends of the TFG cDNA probe hybridized to a 2.2-kb band on Northern blot filters in all tissues examined.

摘要

在表达序列标签数据库中进行同源性搜索时,使用富含SPYGQ的区域作为查询序列,以寻找编码与肉瘤相关EWS和FUS蛋白N端部分相似的蛋白质区域的基因。选择了在其5'端编码富含SPYGQ区域的克隆22911(T74973)以及其他几个与22911重叠的克隆。合并后的数据使得组装全长cDNA序列成为可能。该cDNA序列为1677 bp,包含起始密码子ATG、一个400个氨基酸的开放阅读框、一个聚腺苷酸信号和一个聚腺苷酸尾。我们发现共有序列的5'部分与名为TFG的598 bp长序列之间具有100%的同一性。TFG序列与NTRK1的3'端融合,产生在甲状腺乳头状癌中发现的TRK-T3融合转录本。因此,该cDNA代表TFG基因的全长转录本。通过荧光原位杂交将TFG定位于3q11-q12。在所有检测的组织中,TFG cDNA探针的3'端和5'端与Northern杂交滤膜上的一条2.2 kb条带杂交。

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