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 PMID:23658642  

AKAP13 Rho-GEF and PKD-binding domain deficient mice develop normally but have an abnormal response to β-adrenergic-induced cardiac hypertrophy.

Matthew J Spindler | Brian T Burmeister | Yu Huang | Edward C Hsiao | Nathan Salomonis | Mark J Scott | Deepak Srivastava | Graeme K Carnegie | Bruce R Conklin
PloS one | 2013

A-kinase anchoring proteins (AKAPs) are scaffolding molecules that coordinate and integrate G-protein signaling events to regulate development, physiology, and disease. One family member, AKAP13, encodes for multiple protein isoforms that contain binding sites for protein kinase A (PKA) and D (PKD) and an active Rho-guanine nucleotide exchange factor (Rho-GEF) domain. In mice, AKAP13 is required for development as null embryos die by embryonic day 10.5 with cardiovascular phenotypes. Additionally, the AKAP13 Rho-GEF and PKD-binding domains mediate cardiomyocyte hypertrophy in cell culture. However, the requirements for the Rho-GEF and PKD-binding domains during development and cardiac hypertrophy are unknown.

Pubmed ID: 23658642

Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL089707
  • Agency: NIAMS NIH HHS, United States
    Id: 7 K08 AR056299-02
  • Agency: NCRR NIH HHS, United States
    Id: RR18928
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL072742
  • Agency: NCATS NIH HHS, United States
    Id: UL1 TR000050
  • Agency: NHLBI NIH HHS, United States
    Id: P01HL089707
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL60664
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL060664
  • Agency: NCRR NIH HHS, United States
    Id: C06 RR018928
  • Agency: NHLBI NIH HHS, United States
    Id: U01 HL100406
  • Agency: NIAMS NIH HHS, United States
    Id: K08 AR056299
  • Agency: NHLBI NIH HHS, United States
    Id: UO1 HL100406
  • Agency: NHLBI NIH HHS, United States
    Id: 5T32HL072742-09

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International Gene Trap Consortium (tool)

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