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Splicing analysis of STAT3 tandem donor suggests non-canonical binding registers for U1 and U6 snRNAs

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F65269705%3A_____%2F24%3A00079593" target="_blank" >RIV/65269705:_____/24:00079593 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216224:14110/24:00136122 RIV/00209775:_____/24:N0000016

  • Result on the web

    <a href="https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkae147/7617147?login=true" target="_blank" >https://academic.oup.com/nar/advance-article/doi/10.1093/nar/gkae147/7617147?login=true</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1093/nar/gkae147" target="_blank" >10.1093/nar/gkae147</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Splicing analysis of STAT3 tandem donor suggests non-canonical binding registers for U1 and U6 snRNAs

  • Original language description

    Tandem donor splice sites (5 &apos; ss) are unique regions with at least two GU dinucleotides serving as splicing cleavage sites. The Delta 3 tandem 5 &apos; ss are a specific subclass of 5 &apos; ss separated by 3 nucleotides which can affect protein function by inserting/deleting a single amino acid. One 5 &apos; ss is typically preferred, yet factors governing particular 5 &apos; ss choice are not fully understood. A highly conserved exon 21 of the STAT3 gene was chosen as a model to study Delta 3 tandem 5 &apos; ss splicing mechanisms. Based on multiple lines of experimental evidence, endogenous U1 snRNA most likely binds only to the upstream 5 &apos; ss. However, the downstream 5 &apos; ss is used preferentially, and the splice site choice is not dependent on the exact U1 snRNA binding position. Downstream 5 &apos; ss usage was sensitive to exact nucleotide composition and dependent on the presence of downstream regulatory region. The downstream 5 &apos; ss usage could be best explained by two novel interactions with endogenous U6 snRNA. U6 snRNA enables the downstream 5 &apos; ss usage in STAT3 exon 21 by two mechanisms: (i) binding in a novel non-canonical register and (ii) establishing extended Watson-Crick base pairing with the downstream regulatory region. This study suggests that U6:5 &apos; ss interaction is more flexible than previously thought. Graphical Abstract

  • 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

    <a href="/en/project/LM2018132" target="_blank" >LM2018132: The National Center for Medical Genomic</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2024

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Nucleic Acids Research

  • ISSN

    0305-1048

  • e-ISSN

    1362-4962

  • Volume of the periodical

    52

  • Issue of the periodical within the volume

    10

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    16

  • Pages from-to

    5959-5974

  • UT code for WoS article

    001176086700001

  • EID of the result in the Scopus database

    2-s2.0-85195778811