Zebrafish cohesin protein Sgo1 is required for cardiac function and eye development

Date of news: 24 March 2022

In collaboration with researchers from the Hubrecht Institute in Utrecht, Sanne Broekman and Erwin van Wijk generated a zebrafish model of Sgo1 that showed its importance during organ development and function.

Cohesinopathies is a term that refers to genetic diseases caused by mutations in the cohesin complex proteins. The cohesin complex is a multiprotein complex that facilitates different aspects of cell division, gene transcription, DNA damage repair, and chromosome architecture. Shugoshin proteins prevent the cohesin complex from premature dissociation from chromatids during cell division. Patients with a homozygous missense mutation in SGO1, which encodes for Shugoshin1, have problems with normal pacing of the heart and gut.

To study the role of shugoshin during embryo development the zebrafish sgo1 gene was mutated. Homozygous sgo1 mutant embryos display various phenotypes related to different organs, including a reduced heart rate accompanied by reduced cardiac function. In addition, sgo1 mutants are vision-impaired as a consequence of structurally defective and partially non-functional photoreceptor cells. Furthermore, the sgo1 mutants display reduced food intake and early lethality.

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