T gene isoform expression pattern is significantly different between chordomas and notochords

Biochem Biophys Res Commun. 2015 Nov 13;467(2):261-7. doi: 10.1016/j.bbrc.2015.09.178. Epub 2015 Oct 3.

Abstract

The T gene plays a key role in chordoma pathology. To investigate the role of T gene isoforms in chordoma, 22 skull base chordomas, three chordoma cell lines and 9 infant notochords, which were used as normal controls, were collected. We first conducted droplet digital PCR to quantify the absolute expression levels of the long and short isoforms of the T gene (T-long and T-short, respectively) and revealed that T-long was dominantly expressed in all chordomas and chordoma cell lines, but not in the notochords. The T-long/T-short ratio was significantly different between the chordomas and the notochords. Next, we validated the isoform expression pattern at protein expression level using Western blot in 9 chordomas. Furthermore, the T gene single nucleotide polymorphism site rs2305089, which is the only marker reported to be associated with chordomas, was sequenced in all of the chordoma samples. Association between rs2305089 and T-long/T-short ratio was not significant, indicating it was not involved in T gene alternative splicing. In conclusion, two T gene isoforms were investigated in skull base chordomas and chordoma cell lines, and the longer isoform was dominantly expressed. The distinct expression patterns of these T gene isoforms may contribute to the pathogenesis of skull base chordomas. However, further studies on the function of these isoforms are needed.

Keywords: Brachyury; Chordoma; Isoform; T gene.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Alternative Splicing
  • Cell Line, Tumor
  • Child
  • Chordoma / diagnosis
  • Chordoma / genetics*
  • Chordoma / metabolism
  • Chordoma / pathology
  • Fetal Proteins / genetics*
  • Fetal Proteins / metabolism
  • Fetus
  • Gene Expression
  • Humans
  • Male
  • Middle Aged
  • Notochord / metabolism*
  • Polymorphism, Single Nucleotide
  • Protein Isoforms / genetics
  • Protein Isoforms / metabolism
  • Skull Base Neoplasms / diagnosis
  • Skull Base Neoplasms / genetics*
  • Skull Base Neoplasms / metabolism
  • Skull Base Neoplasms / pathology
  • T-Box Domain Proteins / genetics*
  • T-Box Domain Proteins / metabolism

Substances

  • Fetal Proteins
  • Protein Isoforms
  • T-Box Domain Proteins
  • Brachyury protein