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

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Base Sequence
  • Chromosome Mapping
  • Chromosomes, Human, Pair 3 / genetics
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Gene Expression
  • Humans
  • In Situ Hybridization, Fluorescence
  • Molecular Sequence Data
  • Proteins / genetics*
  • Thyroid Neoplasms / genetics*

Substances

  • DNA, Complementary
  • Proteins
  • TFG protein, human

Associated data

  • GENBANK/Y07968