TM2D genes regulate Notch signaling and neuronal function in Drosophila

Author:

Salazar Jose L.ORCID,Yang Sheng-AnORCID,Lin Yong Qi,Li-Kroeger DavidORCID,Marcogliese Paul C.ORCID,Deal Samantha L.ORCID,Neely G. GregoryORCID,Yamamoto ShinyaORCID

Abstract

TM2 domain containing (TM2D) proteins are conserved in metazoans and encoded by three separate genes in each model organism species that has been sequenced. Rare variants in TM2D3 are associated with Alzheimer’s disease (AD) and its fly ortholog almondex is required for embryonic Notch signaling. However, the functions of this gene family remain elusive. We knocked-out all three TM2D genes (almondex, CG11103/amaretto, CG10795/biscotti) in Drosophila and found that they share the same maternal-effect neurogenic defect. Triple null animals are not phenotypically worse than single nulls, suggesting these genes function together. Overexpression of the most conserved region of the TM2D proteins acts as a potent inhibitor of Notch signaling at the γ-secretase cleavage step. Lastly, Almondex is detected in the brain and its loss causes shortened lifespan accompanied by progressive motor and electrophysiological defects. The functional links between all three TM2D genes are likely to be evolutionarily conserved, suggesting that this entire gene family may be involved in AD.

Funder

National Institute on Aging

Alzheimer's Association

Nancy Chang, Ph.D. Award for Research Excellence

National Institute of General Medical Sciences

CIHR

Intellectual and Developmental Disabilities Research Center

Publisher

Public Library of Science (PLoS)

Subject

Cancer Research,Genetics (clinical),Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

Reference105 articles.

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