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Functional role of Sec20, a BH3 and Secretory (Sec) domain protein, in neurons and its relevance to a motor neuron disease in Drosophila

Award Number: R01NS131315
ORGANIZATION: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE
OPDIV: NIH
AWARD CLASS: DISCRETIONARY
AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)
PERIOD OF PERFORMANCE START DATE: 04/15/2023
PERIOD OF PERFORMANCE END DATE: 03/31/2028

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Functional role of Sec20, a BH3 and Secretory (Sec) domain protein, in neurons and its relevance to a motor neuron disease in Drosophila - This proposal examines the functional role of Sec20, a BH3 and Secretory (Sec) domain protein, in neurons and its relevance to a motor neuron disease using Drosophila. It also examines the interaction between sec20 and GGGGCC (G4C2) repeats of the gene C9orf72 (Chromosome9 open reading frame), a well- known mutation that causes Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal dementia (FTD) in humans. ALS-FTD are two progressive, adult-onset neurodegenerative diseases, often occurring together. The particular focus of this proposal is neuronal loss and mitochondrial and autophagy defects in the brain. Dysfunctional mitochondria and autophagic failures have emerged as important factors in neurodegenerative diseases. They may actively mediate these diseases or exacerbate them. sec20 is the ortholog of vertebrate Bnip1 gene, which is a member of the Bcl2 interacting protein family. Bnip1 has been tentatively identified as a risk factor for ALS and FTD in humans. We found that loss of function for sec20 in the CNS in Drosophila caused severe motor neuron disease and death. There was neuronal loss, mitochondrial dysfunction and autophagic failures in these flies. The disease and these molecular features had similarities to the motor deficits disease caused by the expression of G4C2 repeats. The phenotypes caused by the G4C2 repeats were upstream of sec20 in flies as well as in humans. Thus, our specific aims are: 1) Determine the molecular basis for the loss of motor neurons in sec20 mutant flies, 2) Determine if defective mitophagy and autophagy in sec20 mutants contribute to the disease, and 3) Delineate the interaction between sec20 and the c9orf72-G4C2-R in the CNS. In Drosophila, we go from phenotypes to genes and then molecular underpinnings. There is always a bottom line with this system. Our aims investigate the basics of the phenotypes caused by these genes/mutations. These studies will help understand the function of Sec20 in the CNS and how it relates to G4C2 repeats in the biology and in the diseases of the brain.


Issue Date FY	Funding FY	Legal Entity Name	Legal Entity Address	Legal Entity City	Legal Entity State	Legal Entity Zip Code	Legal Entity COUNTY	Legal Entity COUNTRY	Assistance Listing	Award Code	Budget Year	Action Date	Action Type	Action Amount

Issue Date FY: 2026 ( Subtotal = $469,350 )
2026	2026	UNIVERSITY OF ALABAMA AT BIRMINGHAM	701 S 20TH STREET	BIRMINGHAM	AL	35294	JEFFERSON	USA	Extramural Research Programs in the Neurosciences and Neurological Disorders	000	3	4/3/2026	EXTENSION WITH OR WITHOUT FUNDS	$469,350
														Subtotal = $469,350

Grand Total All Awards = $469,350

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Functional role of Sec20, a BH3 and Secretory (Sec) domain protein, in neurons and its relevance to a motor neuron disease in Drosophila

Award Number: R01NS131315

ORGANIZATION: NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE

OPDIV: NIH

AWARD CLASS: DISCRETIONARY

AWARD ACTIVITY TYPE: SCIENTIFIC/HEALTH RESEARCH (INCLUDES SURVEYS)

PERIOD OF PERFORMANCE START DATE: 04/15/2023

PERIOD OF PERFORMANCE END DATE: 03/31/2028

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