The Arthropoda-specific Tramtrack group BTB protein domains use previously unknown interface to form hexamers

Artem N. Bonchuk, Konstantin I. Balagurov, Rozbeh Baradaran, Konstantin M. Boyko, Nikolai N. Sluchanko, Anastasia M. Khrustaleva, Anna D. Burtseva, Olga V. Arkova, Karina K. Khalisova, Vladimir O. Popov, Andreas Naschberger, Pavel G. Georgiev

Research output: Contribution to journalArticlepeer-review

Abstract

BTB (bric-a-brack, Tramtrack, and broad complex) is a diverse group of protein-protein interaction domains found within metazoan proteins. Transcription factors contain a dimerizing BTB subtype with a characteristic N-terminal extension. The Tramtrack group (TTK) is a distinct type of BTB domain, which can multimerize. Single-particle cryo-EM microscopy revealed that the TTK-type BTB domains assemble into a hexameric structure consisting of three canonical BTB dimers connected through a previously uncharacterized interface. We demonstrated that the TTK-type BTB domains are found only in Arthropods and have undergone lineage-specific expansion in modern insects. The Drosophila genome encodes 24 transcription factors with TTK-type BTB domains, whereas only four have non-TTK-type BTB domains. Yeast two-hybrid analysis revealed that the TTK-type BTB domains have an unusually broad potential for heteromeric associations presumably through a dimer-dimer interaction interface. Thus, the TTK-type BTB domains are a structurally and functionally distinct group of protein domains specific to Arthropodan transcription factors.

Original languageEnglish (US)
JournaleLife
Volume13
DOIs
StatePublished - Sep 2 2024

Keywords

  • Cryo-EM
  • D. melanogaster
  • molecular biophysics
  • SAXS
  • structural biology
  • transcription factors

ASJC Scopus subject areas

  • General Neuroscience
  • General Biochemistry, Genetics and Molecular Biology
  • General Immunology and Microbiology

Fingerprint

Dive into the research topics of 'The Arthropoda-specific Tramtrack group BTB protein domains use previously unknown interface to form hexamers'. Together they form a unique fingerprint.

Cite this