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Alternative splicing of T-box transcription factor genes

  • Paige DeBenedittis
    ,
  • Kai Jiao(corresponding author)
*Corresponding author for this work
  • University of Alabama at Birmingham
Scholary Output:
Contribution to journal
Short survey
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

T-box (TBX) transcription factors are an ancient gene family with critical roles in embryogenesis. Currently, TBX3, TBX5, and TBX20 are TBX genes defined to have multiple protein isoforms created by alternative splicing and characterized by expression and functional studies. These proteins are important for development as mutations lead to severe developmental disorders in humans and mice. Cumulative studies suggest that alternative splicing of these genes can regulate TBX activities during multiple biological processes including cardiogenesis, limb development, and cancer mechanisms. This mini-review focuses on how alternative splicing adds complexity to transcriptional regulation of target genes controlled by TBX transcription factors.

Publication Information

Output type

Scholary Output:
Contribution to journal
Short survey
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 513-517 (5 pages)

Journal (Volume, Issue Number)

Biochemical and Biophysical Research Communications (Volume 412, Issue 4)

Publication milestones

  • Published - 09/09/2011

Publication status

Published - 09/09/2011

ISSN

0006-291X

Publication IDs

  • Scopus: 80052627592
  • PubMed: 21856288

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Funding Details

We regret that we could not reference all studies in this area due to space limitations. The work in KJ’s lab is supported by a UAB Faculty Development Grant and a NHLBI R01 Grant ( HL095783-01A1 ) awarded to KJ.
FundersFunding number
NHLBI
R01HL095783
UAB
-