Coiled-coil motif as a structural basis for the interaction of HTLV type 1 Tax with cellular cofactors

AIDS Res Hum Retroviruses. 2000 Nov 1;16(16):1689-94. doi: 10.1089/08892220050193155.

Abstract

Human T lymphotropic virus type 1 (HTLV-1) Tax is a multifunctional protein centrally involved in transcriptional regulation, cell cycle control, and viral transformation. The regulatory functions of Tax are thought to be mediated through protein-protein interaction with cellular cofactors. Previously we have identified several novel binding partners for Tax, including human mitotic checkpoint protein MAD1 (TXBP181), G-protein pathway suppressor GPS2 (TXBP31), and IkappaB kinase regulatory subunit IKK-gamma. Here we described two additional Tax partners, TXBP151 and TXBP121. A closer examination of the sequences of eight independent cellular Tax-binding proteins identified by us and others revealed that all of them share a single characteristic, a highly structured coiled-coil domain. We also noted that Tax and the Tax-binding coiled-coil proteins can homodimerize. Additionally, the same domain in Tax is responsible for interaction with different coiled-coil proteins. Taken together, our findings point to a particular coiled-coil structure as one of the Tax-recognition motifs. The interaction of Tax with a particular subgroup of cellular coiled-coil proteins represents one mechanism by which Tax dysregulates cell growth and proliferation.

MeSH terms

  • Amino Acid Motifs
  • Amino Acid Sequence
  • Carrier Proteins / chemistry
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Cell Cycle Proteins
  • Dimerization
  • Gene Products, tax / chemistry*
  • Gene Products, tax / genetics
  • Gene Products, tax / metabolism*
  • Human T-lymphotropic virus 1 / metabolism
  • Humans
  • I-kappa B Kinase
  • Intracellular Signaling Peptides and Proteins*
  • Mutation
  • Neoplasm Proteins*
  • Nuclear Proteins
  • Phosphoproteins / chemistry
  • Phosphoproteins / genetics
  • Phosphoproteins / metabolism
  • Plasmids / genetics
  • Protein Serine-Threonine Kinases / chemistry
  • Protein Serine-Threonine Kinases / metabolism
  • Repressor Proteins / chemistry
  • Repressor Proteins / genetics
  • Repressor Proteins / metabolism
  • Structure-Activity Relationship
  • Two-Hybrid System Techniques

Substances

  • Carrier Proteins
  • Cell Cycle Proteins
  • GPS2 protein, human
  • Gene Products, tax
  • Intracellular Signaling Peptides and Proteins
  • MAD1L1 protein, human
  • Neoplasm Proteins
  • Nuclear Proteins
  • Phosphoproteins
  • Repressor Proteins
  • TAX1BP1 protein, human
  • Protein Serine-Threonine Kinases
  • CHUK protein, human
  • I-kappa B Kinase
  • IKBKB protein, human
  • IKBKE protein, human