HAND transcription factors cooperatively specify the aorta and pulmonary trunk.

Vincentz, Joshua W; Firulli, Beth A; Toolan, Kevin P; Osterwalder, Marco; Pennacchio, Len A; Firulli, Anthony B (2021). HAND transcription factors cooperatively specify the aorta and pulmonary trunk. Developmental biology, 476, pp. 1-10. Elsevier 10.1016/j.ydbio.2021.03.011

[img] Text
1-s2.0-S0012160621000737-main.pdf - Published Version
Restricted to registered users only
Available under License Publisher holds Copyright.

Download (4MB) | Request a copy

Congenital heart defects (CHDs) affecting the cardiac outflow tract (OFT) constitute a significant cause of morbidity and mortality. The OFT develops from migratory cell populations which include the cardiac neural crest cells (cNCCs) and secondary heart field (SHF) derived myocardium and endocardium. The related transcription factors HAND1 and HAND2 have been implicated in human CHDs involving the OFT. Although Hand1 is expressed within the OFT, Hand1 NCC-specific conditional knockout mice (H1CKOs) are viable. Here we show that these H1CKOs present a low penetrance of OFT phenotypes, whereas SHF-specific Hand1 ablation does not reveal any cardiac phenotypes. Further, HAND1 and HAND2 appear functionally redundant within the cNCCs, as a reduction/ablation of Hand2 on an NCC-specific H1CKO background causes pronounced OFT defects. Double conditional Hand1 and Hand2 NCC knockouts exhibit persistent truncus arteriosus (PTA) with 100% penetrance. NCC lineage-tracing and Sema3c in situ mRNA expression reveal that Sema3c-expressing cells are mis-localized, resulting in a malformed septal bridge within the OFTs of H1CKO;H2CKO embryos. Interestingly, Hand1 and Hand2 also genetically interact within the SHF, as SHF H1CKOs on a heterozygous Hand2 background exhibit Ventricular Septal Defects (VSDs) with incomplete penetrance. Previously, we identified a BMP, HAND2, and GATA-dependent Hand1 OFT enhancer sufficient to drive reporter gene expression within the nascent OFT and aorta. Using these transcription inputs as a probe, we identify a novel Hand2 OFT enhancer, suggesting that a conserved BMP-GATA dependent mechanism transcriptionally regulates both HAND factors. These findings support the hypothesis that HAND factors interpret BMP signaling within the cNCCs to cooperatively coordinate OFT morphogenesis.

Item Type:

Journal Article (Original Article)

Division/Institute:

04 Faculty of Medicine > Pre-clinic Human Medicine > BioMedical Research (DBMR)

UniBE Contributor:

Osterwalder, Marco

Subjects:

600 Technology > 610 Medicine & health

ISSN:

0012-1606

Publisher:

Elsevier

Language:

English

Submitter:

Marla Rittiner

Date Deposited:

24 Jan 2022 09:22

Last Modified:

05 Dec 2022 16:00

Publisher DOI:

10.1016/j.ydbio.2021.03.011

PubMed ID:

33757801

Uncontrolled Keywords:

Cardiac neural crest Cardiac outflow track Congenital heart defects HAND1 HAND2 Second heart field Transcription bHLH transcription factors

BORIS DOI:

10.48350/163435

URI:

https://boris.unibe.ch/id/eprint/163435

Actions (login required)

Edit item Edit item
Provide Feedback