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Transposable element landscape changes are buffered by RNA silencing in aging Drosophila
by
Srivastav, Satyam P
, Rahman, Reazur
, Chinen, Madoka
, Lei, Elissa P
, Ma, Qicheng
, Rosbash, Michael
, Lau, Nelson C
, Yang, Nachen
, Dayama, Gargi
in
Aging
/ DNA sequencing
/ Drosophila
/ Genomics
/ Insects
/ Life span
/ RNA-mediated interference
/ Transposons
/ Whole genome sequencing
2021
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Transposable element landscape changes are buffered by RNA silencing in aging Drosophila
by
Srivastav, Satyam P
, Rahman, Reazur
, Chinen, Madoka
, Lei, Elissa P
, Ma, Qicheng
, Rosbash, Michael
, Lau, Nelson C
, Yang, Nachen
, Dayama, Gargi
in
Aging
/ DNA sequencing
/ Drosophila
/ Genomics
/ Insects
/ Life span
/ RNA-mediated interference
/ Transposons
/ Whole genome sequencing
2021
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
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Transposable element landscape changes are buffered by RNA silencing in aging Drosophila
by
Srivastav, Satyam P
, Rahman, Reazur
, Chinen, Madoka
, Lei, Elissa P
, Ma, Qicheng
, Rosbash, Michael
, Lau, Nelson C
, Yang, Nachen
, Dayama, Gargi
in
Aging
/ DNA sequencing
/ Drosophila
/ Genomics
/ Insects
/ Life span
/ RNA-mediated interference
/ Transposons
/ Whole genome sequencing
2021
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Transposable element landscape changes are buffered by RNA silencing in aging Drosophila
Paper
Transposable element landscape changes are buffered by RNA silencing in aging Drosophila
2021
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Overview
ABSTRACT Genetic mechanisms that repress transposable elements (TEs) in young animals decline during aging, as reflected by increased TE expression in aged animals. Does increased TE expression during aging lead to more genomic TE copies in older animals? To answer this question, we quantified TE Landscapes (TLs) via whole genome sequencing of young and aged Drosophila strains of wild-type and mutant backgrounds. We quantified TLs in whole flies and dissected brains and validated the feasibility of our approach in detecting new TE insertions in aging Drosophila genomes when natural defenses like RNA interference (RNAi) pathways are compromised. By also incorporating droplet digital PCR to validate genomic TE loads, we confirm TL changes can occur in a single lifespan of Drosophila when TEs are not suppressed. We also describe improved sequencing methods to quantify extra-chromosomal DNA circles (eccDNAs) in Drosophila as an additional source of TE copies that accumulate during aging. Lastly, to combat the natural progression of aging-associated TE expression, we show that knocking down PAF1, a conserved transcription elongation factor that antagonizes RNAi pathways, may bolster suppression of TEs during aging and extend lifespan. Our study suggests that RNAi mechanisms generally mitigate genomic TL expansion despite the increase in TE transcripts during aging.
Publisher
Cold Spring Harbor Laboratory Press,Cold Spring Harbor Laboratory
Subject
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