Knockout of the longevity gene Klotho perturbs aging and Alzheimer’s disease-linked brain microRNAs and tRNA fragments

Serafima Dubnov(Hebrew University of Jerusalem), Estelle R. Bennett(Hebrew University of Jerusalem), Nadav Yayon(European Bioinformatics Institute), Or Yakov(Hebrew University of Jerusalem), David A. Bennett(Rush University Medical Center), Sudha Seshadri(The University of Texas at San Antonio Health Science Center), Elliott J. Mufson(Barrow Neurological Institute), Yonat Tzur(Hebrew University of Jerusalem), David Greenberg(Hebrew University of Jerusalem), Makoto Kuro‐o(Jichi Medical University), Iddo Paldor(Hebrew University of Jerusalem), Carmela R. Abraham(Boston University), Hermona Soreq(Hebrew University of Jerusalem)
Communications Biology
June 11, 2024
Cited by 21Open Access
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Abstract

Overexpression of the longevity gene Klotho prolongs lifespan, while its knockout shortens lifespan and impairs cognition via perturbation of myelination and synapse formation. However, comprehensive analysis of Klotho knockout effects on mammalian brain transcriptomics is lacking. Here, we report that Klotho knockout alters the levels of aging- and cognition related mRNAs, long non-coding RNAs, microRNAs and tRNA fragments. These include altered neuronal and glial regulators in murine models of aging and Alzheimer's disease and in human Alzheimer's disease post-mortem brains. We further demonstrate interaction of the knockout-elevated tRNA fragments with the spliceosome, possibly affecting RNA processing. Last, we present cell type-specific short RNA-seq datasets from FACS-sorted neurons and microglia of live human brain tissue demonstrating in-depth cell-type association of Klotho knockout-perturbed microRNAs. Together, our findings reveal multiple RNA transcripts in both neurons and glia from murine and human brain that are perturbed in Klotho deficiency and are aging- and neurodegeneration-related.


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