Polymorphic structure of the tumor necrosis factor (TNF) locus: an NcoI polymorphism in the first intron of the human TNF-beta gene correlates with a variant amino acid in position 26 and a reduced level of TNF-beta production

J Exp Med. 1991 Jan 1;173(1):209-19. doi: 10.1084/jem.173.1.209.

Abstract

Since a dysregulated synthesis of tumor necrosis factor alpha (TNF-alpha) may be involved in the pathogenesis of autoimmune diseases, it was of interest to precisely locate the recently reported NcoI restriction fragment length polymorphism (RFLP) of the TNF-alpha region. However, by mapping of 56.8 kb of overlapping cosmid clones and direct sequencing, we could localize the polymorphic NcoI restriction site within the first intron of the TNF-beta gene and not in the TNF-alpha gene. To study whether regulatory mechanisms are affected by this polymorphism, we analyzed the TNF-alpha/TNF-beta production of phytohemagglutinin-stimulated peripheral blood mononuclear cells of individuals homozygous for the TNF-beta NcoI RFLP by ELISA and concomitant Northern blot analysis. On days 2-4 after stimulation with mitogen, the TNFB*1 allele corresponding to a 5.3-kb NcoI fragment presented with a significantly higher TNF-beta response. A mRNA analysis demonstrated that higher protein levels of TNF-beta correlate also with increased amounts of TNF-beta transcripts. No allelic association was found in respect to TNF-alpha production. To further investigate a possible allelic influence on transcription, we determined the DNA sequence of 2 kb of the 5' portion of our cloned TNFB*2 allele and compared it with the available TNF-beta sequences. By computer-aided recognition motif search of DNA binding factors, we report putative binding sites conserved between mouse and man in the 5' flanking region as well as in intron 1 of the TNF-beta gene, found also in other cytokine promoter sequences. In addition, by polymerase chain reaction amplification and sequencing of 740 bp of the 5' part of TNF-beta of individuals typed homozygously for the NcoI RFLP, we could show that amino acid position 26 is conserved as asparagine in the TNFB*1 and as threonine in the TNFB*2 sequence. A previously reported, EcoRI RFLP in the 3' untranslated region of TNF-beta does not segregate with either of the two alleles. Thus, four TNFB alleles can be defined at the DNA level.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • Deoxyribonuclease EcoRI
  • Deoxyribonucleases, Type II Site-Specific
  • Gene Expression Regulation / genetics
  • Humans
  • Introns / genetics
  • Lymphocyte Activation / drug effects
  • Lymphocytes / drug effects
  • Lymphocytes / metabolism
  • Lymphotoxin-alpha / biosynthesis
  • Lymphotoxin-alpha / genetics*
  • Molecular Sequence Data
  • Phytohemagglutinins / pharmacology
  • Polymorphism, Restriction Fragment Length
  • Promoter Regions, Genetic / genetics
  • Restriction Mapping
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Lymphotoxin-alpha
  • Phytohemagglutinins
  • Tumor Necrosis Factor-alpha
  • Deoxyribonuclease EcoRI
  • endodeoxyribonuclease NcoI
  • Deoxyribonucleases, Type II Site-Specific

Associated data

  • GENBANK/X55424
  • GENBANK/X55425
  • GENBANK/X55426
  • GENBANK/X55427
  • GENBANK/X58209
  • GENBANK/X58210
  • GENBANK/X59351
  • GENBANK/X59352
  • GENBANK/X60276
  • GENBANK/X60277