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Deshwar, A. R.

Publications and source records attributed to Deshwar, A. R..

2 recordsLinked to original sources

Role of the obligate STRIPAK complex component Mob4 in zebrafish vascular development and stability

The STRiatin Interacting Phosphatases and Kinases (STRIPAK) complex is a conserved multiprotein module with functions in cell proliferation, cell growth, and cancer. Primarily examined through proteomic and in vitro studies, there is a relative lack of insight into the in vivo function of the STRIPAK complex during development. Motivated by the prominent interaction of STRIPAK and the CCM3 adapter protein, which is associated with the vascular disease cerebral cavernous malformation (CCM), we sought to examine the role of the conserved STRIPAK component Mob4 in early zebrafish vascular development. We use proximity-dependent biotinylation (BioID) coupled with mass spectrometry to show that Mob4 is a component of the STRIPAK complex in zebrafish. Loss of mob4 leads to pronounced cardiovascular and neuronal defects, including a leaky cerebral vasculature, hypersprouting of venous endothelial cells and poor neuronal branching. Conditional transgenic models further demonstrate a continuous and broad requirement for Mob4 in development. Taken together, these results suggest a key role for STRIPAK function in vascular development and stability, replicating hallmarks of CCM.

developmental biology↗

Hey2 restricts cardiac progenitor addition to the developing heart

A key event in vertebrate heart development is the timely addition of second heart field (SHF) progenitor cells to the poles of the heart tube. This accretion process must occur to the proper extent to prevent a spectrum of congenital heart defects (CHDs). However, the factors that regulate this critical process are poorly understood. Here we demonstrate that Hey2, a bHLH transcriptional repressor, restricts SHF progenitor accretion to the zebrafish heart. hey2 expression demarcated a distinct domain within the cardiac progenitor population. In the absence of Hey2 function an increase in myocardial cell number and SHF progenitors was observed. We found that Hey2 limited proliferation of SHF-derived cardiomyocytes in a cell-autonomous manner, prior to heart tube formation, and further restricted the developmental window over which SHF progenitors were deployed to the heart. Taken together, our data suggests a role for Hey2 in controlling the proliferative capacity and cardiac contribution of late-differentiating cardiac progenitors.

developmental biology↗