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Multivalency regulates activity in an intrinsically disordered transcription factor

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14740%2F18%3A00106665" target="_blank" >RIV/00216224:14740/18:00106665 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.7554/eLife.36258" target="_blank" >http://dx.doi.org/10.7554/eLife.36258</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.7554/eLife.36258" target="_blank" >10.7554/eLife.36258</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Multivalency regulates activity in an intrinsically disordered transcription factor

  • Original language description

    The transcription factor ASCIZ (ATMIN, ZNF822) has an unusually high number of recognition motifs for the product of its main target gene, the hub protein LC8 (DYNLL1). Using a combination of biophysical methods, structural analysis by NMR and electron microscopy, and cellular transcription assays, we developed a model that proposes a concerted role of intrinsic disorder and multiple LC8 binding events in regulating LC8 transcription. We demonstrate that the long intrinsically disordered C -terminal domain of ASCIZ binds LC8 to form a dynamic ensemble of complexes with a gradient of transcriptional activity that is inversely proportional to LC8 occupancy. The preference for low occupancy complexes at saturating LC8 concentrations with both human and Drosophila ASCIZ indicates that negative cooperativity is an important feature of ASCIZ-LC8 interactions. The prevalence of intrinsic disorder and multivalency among transcription factors suggests that formation of heterogeneous, dynamic complexes is a widespread mechanism for tuning transcriptional regulation.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2018

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    elife

  • ISSN

    2050-084X

  • e-ISSN

  • Volume of the periodical

    7

  • Issue of the periodical within the volume

    MAY

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    28

  • Pages from-to

    1-28

  • UT code for WoS article

    000432725100001

  • EID of the result in the Scopus database

    2-s2.0-85051995414