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Title: IPLA2-VIA is required for healthy aging of neurons, muscle, and the female germline in Drosophila melanogaster.
Authors: Steinhauer, Josefa
Banerjee, Surya Jyoti
Schonbrun, Adina
Eizadshenass, Sogol
Benji, Shimshon
Cantor, Yaakov Tzvi
Eliach, Liam
Lubin, Matthew
Narrowe, Zev
Purow, Jeremy
Shulman, Benjamin
Wiener, Leib
Keywords: Neurodegenerative disease (ND)
calcium-independent phospholipase A2 (iPLA2)
Issue Date: 10-Jul-2021
Publisher: PLOS: Public Library of Science
Citation: Banerjee, S. J., Schonbrun, A., Eizadshenass, S., Benji, S., Cantor, Y. T., Eliach, L., Lubin, M., Narrowe, Z., Purow, J., Shulman, B., Wiener, L., & Steinhauer, J. (2021). IPLA2-VIA is required for healthy aging of neurons, muscle, and the female germline in Drosophila melanogaster. PloS One, 16(9), e0256738.
Series/Report no.: PloS One;16(9)
Abstract: Neurodegenerative disease (ND) is a growing health burden worldwide, but its causes and treatments remain elusive. Although most cases of ND are sporadic, rare familial cases have been attributed to single genes, which can be investigated in animal models. We have generated a new mutation in the calcium-independent phospholipase A2 (iPLA2) VIA gene CG6718, the Drosophila melanogaster ortholog of human PLA2G6/PARK14, mutations in which cause a suite of NDs collectively called PLA2G6-associated neurodegeneration (PLAN). Our mutants display age-related loss of climbing ability, a symptom of neurodegeneration in flies. Although phospholipase activity commonly is presumed to underlie iPLA2- VIA function, locomotor decline in our mutants is rescued by a transgene carrying a serineto- alanine mutation in the catalytic residue, suggesting that important functional aspects are independent of phospholipase activity. Additionally, we find that iPLA2-VIA knockdown in either muscle or neurons phenocopies locomotor decline with age, demonstrating its necessity in both neuronal and non-neuronal tissues. Furthermore, RNA in situ hybridization shows high endogenous iPLA2-VIA mRNA expression in adult germ cells, and transgenic HA-tagged iPLA2-VIA colocalizes with mitochondria there. Mutant males are fertile with normal spermatogenesis, while fertility is reduced in mutant females. Mutant female germ cells display age-related mitochondrial aggregation, loss of mitochondrial potential, and elevated cell death. These results suggest that iPLA2-VIA is critical for mitochondrial integrity in the Drosophila female germline, which may provide a novel context to investigate its functions with parallels to PLAN.
Description: Scholarly article / Open access
ISSN: ISSN: 1932-6203
Appears in Collections:Yeshiva College: Faculty Publications

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