The human TCF-1 gene encodes a nuclear DNA-binding protein uniquely expressed in normal and neoplastic T-lineage lymphocytes

Blood. 1995 Oct 15;86(8):3050-9.

Abstract

The TCF-1 gene encodes a putative transcription factor with affinity for a sequence motif occurring in a number of T-cell enhancers. TCF-1 mRNA was originally found to be expressed in a T cell-specific fashion within a set of human and mouse cell lines. In contrast, expression reportedly occurs in multiple nonlymphoid tissues during murine embryogenesis. We have now raised a monoclonal antibody to document expression and biochemistry of the human TCF-1 protein. As expected, the TCF-1 protein was detectable only in cell lines of T lineage. Its expression was always restricted to the nucleus. Immunohistochemistry on a panel of human tissues revealed that the TCF-1 protein was found exclusively in thymocytes and in CD3+ T cells in peripheral lymphoid tissues. Western blotting yielded a set of bands ranging from 25 kD to 55 kD, resulting from extensive alternative splicing. The TCF-1 protein was detectable in all samples of a set of 22 T-cell malignancies of various stages of maturation, but was absent from a large number of other hematologic neoplasms. These observations imply a T cell-specific function for TCF-1, a notion corroborated by recent observations on Tcf-1 knock-out mice. In addition, these results indicate that nuclear TCF-1 expression can serve as a pan-T-lineage marker in the diagnosis of lymphoid malignancies.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Biomarkers
  • Biomarkers, Tumor / analysis*
  • DNA-Binding Proteins / analysis
  • DNA-Binding Proteins / biosynthesis
  • DNA-Binding Proteins / genetics*
  • Genes
  • Hepatocyte Nuclear Factor 1-alpha
  • Humans
  • Injections, Subcutaneous
  • Leukemia, T-Cell / metabolism*
  • Lymphoid Enhancer-Binding Factor 1
  • Lymphoma, T-Cell / metabolism*
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • Neoplasm Proteins / analysis
  • Neoplasm Proteins / biosynthesis
  • Neoplasm Proteins / genetics*
  • RNA Splicing
  • Recombinant Fusion Proteins / immunology
  • Recombinant Fusion Proteins / metabolism
  • T Cell Transcription Factor 1
  • T-Lymphocytes / metabolism*
  • Transcription Factors / analysis
  • Transcription Factors / biosynthesis
  • Transcription Factors / genetics*

Substances

  • Biomarkers
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • Hepatocyte Nuclear Factor 1-alpha
  • Hnf1a protein, mouse
  • Lymphoid Enhancer-Binding Factor 1
  • Neoplasm Proteins
  • Recombinant Fusion Proteins
  • T Cell Transcription Factor 1
  • TCF7 protein, human
  • Transcription Factors