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Cap analysis of gene expression reveals alternative promoter usage in a rat model of hypertension

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F67985823%3A_____%2F22%3A00555843" target="_blank" >RIV/67985823:_____/22:00555843 - isvavai.cz</a>

  • Result on the web

    <a href="https://doi.org/10.26508/lsa.202101234" target="_blank" >https://doi.org/10.26508/lsa.202101234</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.26508/lsa.202101234" target="_blank" >10.26508/lsa.202101234</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Cap analysis of gene expression reveals alternative promoter usage in a rat model of hypertension

  • Original language description

    The role of alternative promoter usage in tissue-specific gene expression has been well established, however, its role in complex diseases is poorly understood. We performed cap analysis of gene expression (CAGE) sequencing from the left ventricle of a rat model of hypertension, the spontaneously hypertensive rat (SHR), and a normotensive strain, Brown Norway to understand the role of alternative promoter usage in complex disease. We identified 26,560 CAGE-defined transcription start sites in the rat left ventricle, including 1,970 novel cardiac transcription start sites. We identified 28 genes with alternative promoter usage between SHR and Brown Norway, which could lead to protein isoforms differing at the amino terminus between two strains and 475 promoter switching events altering the length of the 5′ UTR. We found that the shift in Insr promoter usage was significantly associated with insulin levels and blood pressure within a panel of HXB/BXH recombinant inbred rat strains, suggesting that hyperinsulinemia due to insulin resistance might lead to hypertension in SHR. Our study provides a preliminary evidence of alternative promoter usage in complex diseases.

  • 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

    2022

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Life Science Alliance

  • ISSN

    2575-1077

  • e-ISSN

    2575-1077

  • Volume of the periodical

    5

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    13

  • Pages from-to

    e202101234

  • UT code for WoS article

    000742638600001

  • EID of the result in the Scopus database

    2-s2.0-85123269301