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Investigating the role of formin FHOD3 during myofibrillogenesis in embryonic chick cardiomyocytes
Journal Title
Keywords
formin
actin
sarcomere
FHOD
FHOD3
cytoskeleton
development
cardiomycoyte
chicken
chick
embryo
sequence
cardiac
heart
chicken embryo
cardiomyocytes
localization
regulation
isoform
myofibril
myocyte
hypertrophic cardiomyopathy
cardiomyopathy
HCM
hypertrophic
embryonic
cell culture
transfection
protein extract
sequencing
actin
sarcomere
FHOD
FHOD3
cytoskeleton
development
cardiomycoyte
chicken
chick
embryo
sequence
cardiac
heart
chicken embryo
cardiomyocytes
localization
regulation
isoform
myofibril
myocyte
hypertrophic cardiomyopathy
cardiomyopathy
HCM
hypertrophic
embryonic
cell culture
transfection
protein extract
sequencing
Readers/Advisors
Pruyne, David W.
Journal Title
Term and Year
Summer 2024
Publication Date
2024-08-05
Book Title
Publication Volume
Publication Issue
Publication Begin
Publication End
Number of pages
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Research Projects
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Abstract
Formins are major actin polymerizing proteins which act via the FH2 domain to promote actin nucleation and polymerization, as well as the FH1 domain to accelerate FH2 mediated actin elongation. FHOD3 is a formin that has been shown to be expressed predominantly in the heart and is critical for myofibril maturation during development in mice. FHOD3 has been shown to localize where actin filaments overlap myosin filaments within the sarcomeres of mice, rat, and human induced pluripotent stem-cell derived cardiomyocytes, flanking both sides of the M-line in the sarcomere. However, the role of FHOD3 in the myofibrillogenesis and the timing of FHOD3's activity in myofibrils has yet to be determined. Using RT-PCR, I successfully identified expression of at least two different isoforms of FHOD3 within heart tissue, matching to predicted isoforms X5 and X6. I also identified two chemically conserved regions within the FHOD3 amino acid sequence that are related to the cardiac FHOD3 isoform's localization to myofibrils. Using immunofluorescence microscopy and western blotting I found that FHOD3 is present within embryonic chick cardiomyocytes and that the localization of FHOD3 matches prior reports. FHOD3 was determined to be transiently expressed at significantly higher rates on Days 3 and 4 of culture in cardiomyocyte myofibrils. 90% of measured sarcomeres containing FHOD3 had a Z-line to Z-line length ranging from 1.4-1.9 µm, suggesting not only a length-dependent role of FHOD3, but a myofibril maturity dependent localization of FHOD3. These observations illustrate that FHOD3 likely does not have a function in the initiation of myofibrillogenesis but may instead have a role in the maturation and elongation of sarcomeres. The transient nature observed also suggests that FHOD3 may be localized within the sarcomere only as needed. Knockdowns of FHOD3 performed with shRNAs showed no indication of knockdown causing myofibrillar disruption. Knockdowns of FHOD3 using DsiRNAs were statistically inconclusive for knockdown occurring but did have an upwards nonsignificant trend in the percentage of myofibril disruption in cardiomyocytes.