Isolation and characterization of AINT: a novel ARNT interacting protein expressed during murine embryonic development

Mech Dev. 2000 Oct;97(1-2):13-26. doi: 10.1016/s0925-4773(00)00415-9.

Abstract

Basic helix-loop-helix-PER-ARNT-SIM (bHLH-PAS) proteins form dimeric transcription factors to mediate diverse biological functions including xenobiotic metabolism, hypoxic response, circadian rhythm and central nervous system midline development. The Ah receptor nuclear translocator protein (ARNT) plays a central role as a common heterodimerization partner. Herein, we describe a novel, embryonically expressed, ARNT interacting protein (AINT) that may be a member of a larger coiled-coil PAS interacting protein family. The AINT C-terminus mediates interaction with the PAS domain of ARNT in yeast and interacts in vitro with ARNT and ARNT2 specifically. AINT localizes to the cytoplasm and overexpression leads to non-nuclear localization of ARNT. A dynamic pattern of AINT mRNA expression during embryogenesis and cerebellum ontogeny supports a role for AINT in development.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Aryl Hydrocarbon Receptor Nuclear Translocator
  • Binding Sites
  • Carrier Proteins / genetics
  • Carrier Proteins / isolation & purification
  • Carrier Proteins / metabolism*
  • Cerebellum / embryology
  • Cloning, Molecular
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Embryonic and Fetal Development
  • Fetal Proteins / genetics
  • Fetal Proteins / isolation & purification
  • Fetal Proteins / metabolism*
  • Gene Expression
  • Helix-Loop-Helix Motifs
  • Humans
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Mice
  • Microtubule-Associated Proteins
  • Molecular Sequence Data
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • RNA, Messenger
  • Receptors, Aryl Hydrocarbon*
  • Saccharomyces cerevisiae
  • Sequence Homology, Amino Acid
  • Signal Transduction
  • Subcellular Fractions
  • Transcription Factors / genetics
  • Transcription Factors / metabolism*
  • Two-Hybrid System Techniques

Substances

  • ARNT protein, human
  • Arnt protein, mouse
  • Carrier Proteins
  • DNA-Binding Proteins
  • Fetal Proteins
  • HIF1A protein, human
  • Hif1a protein, mouse
  • Hypoxia-Inducible Factor 1
  • Hypoxia-Inducible Factor 1, alpha Subunit
  • Microtubule-Associated Proteins
  • Nuclear Proteins
  • RNA, Messenger
  • Receptors, Aryl Hydrocarbon
  • TACC3 protein, mouse
  • Transcription Factors
  • Aryl Hydrocarbon Receptor Nuclear Translocator