Dynamic changes in gene expression through aging in Drosophila melanogaster heads

被引:0
作者
Hanson, Katherine M.
Macdonald, Stuart J. [1 ]
机构
[1] Univ Kansas, Dept Mol Biosci, 1200 Sunnyside Ave, Lawrence, KS 66045 USA
关键词
gene expression; lifespan; aging; gene ontology enrichment; FlyBase; GENOME-WIDE ASSOCIATION; AGE-RELATED-CHANGES; LIFE-SPAN; HUMAN LONGEVITY; OXIDATIVE STRESS; TRANSCRIPTIONAL PROFILE; METABOLISM; MUTATIONS; SURVIVAL; SUBUNIT;
D O I
10.1093/g3journal/jkaf039
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Work in many systems has shown large-scale changes in gene expression during aging. However, many studies employ just 2 arbitrarily chosen timepoints to measure expression and can only observe an increase or a decrease in expression between "young" and "old" animals, failing to capture any dynamic, nonlinear changes that occur throughout the aging process. We used RNA sequencing to measure expression in male head tissue at 15 timepoints through the lifespan of an inbred Drosophila melanogaster strain. We detected >6,000 significant, age-related genes, nearly all of which have been seen in previous Drosophila aging expression studies and that include several known to harbor lifespan-altering mutations. We grouped our gene set into 28 clusters via their temporal expression change, observing a diversity of trajectories; some clusters show a linear change over time, while others show more complex, nonlinear patterns. Notably, reanalysis of our dataset comparing the earliest and latest timepoints-mimicking a 2-timepoint design-revealed fewer differentially expressed genes (around 4,500). Additionally, those genes exhibiting complex expression trajectories in our multitimepoint analysis were most impacted in this reanalysis; their identification, and the inferred change in gene expression with age, was often dependent on the timepoints chosen. Informed by our trajectory-based clusters, we executed a series of gene enrichment analyses, identifying enriched functions/pathways in all clusters, including the commonly seen increase in stress- and immune-related gene expression with age. Finally, we developed a pair of accessible Shiny apps to enable exploration of our differential expression and gene enrichment results.
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页数:15
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共 113 条
[1]   Interplay of dFOXO and Two ETS-Family Transcription Factors Determines Lifespan in Drosophila melanogaster [J].
Alic, Nazif ;
Giannakou, Maria E. ;
Papatheodorou, Irene ;
Hoddinott, Matthew P. ;
Andrews, T. Daniel ;
Bolukbasi, Ekin ;
Partridge, Linda .
PLOS GENETICS, 2014, 10 (09)
[2]   Data on RNA-seq analysis of Drosophila melanogaster during ageing [J].
Bajgiran, Morteza ;
Azlan, Azali ;
Shamsuddin, Shaharum ;
Azzam, Ghows ;
Halim, Mardani Abdul .
DATA IN BRIEF, 2021, 38
[3]   Age-Related Changes of Gene Expression Profiles in Drosophila [J].
Bordet, Guillaume ;
Lodhi, Niraj ;
Kossenkov, Andrew ;
Tulin, Alexei .
GENES, 2021, 12 (12)
[4]   GWAS of Longevity in CHARGE Consortium Confirms APOE and FOXO3 Candidacy [J].
Broer, Linda ;
Buchman, Aron S. ;
Deelen, Joris ;
Evans, Daniel S. ;
Faul, Jessica D. ;
Lunetta, Kathryn L. ;
Sebastiani, Paola ;
Smith, Jennifer A. ;
Smith, Albert V. ;
Tanaka, Toshiko ;
Yu, Lei ;
Arnold, Alice M. ;
Aspelund, Thor ;
Benjamin, Emelia J. ;
De Jager, Philip L. ;
Eirkisdottir, Gudny ;
Evans, Denis A. ;
Garcia, Melissa E. ;
Hofman, Albert ;
Kaplan, Robert C. ;
Kardia, Sharon L. R. ;
Kiel, Douglas P. ;
Oostra, Ben A. ;
Orwoll, Eric S. ;
Parimi, Neeta ;
Psaty, Bruce M. ;
Rivadeneira, Fernando ;
Rotter, Jerome I. ;
Seshadri, Sudha ;
Singleton, Andrew ;
Tiemeier, Henning ;
Uitterlinden, Andre G. ;
Zhao, Wei ;
Bandinelli, Stefania ;
Bennett, David A. ;
Ferrucci, Luigi ;
Gudnason, Vilmundur ;
Harris, Tamara B. ;
Karasik, David ;
Launer, Lenore J. ;
Perls, Thomas T. ;
Slagboom, P. Eline ;
Tranah, Gregory J. ;
Weir, David R. ;
Newman, Anne B. ;
van Duijn, Cornelia M. ;
Murabito, Joanne M. .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2015, 70 (01) :110-118
[5]   Induction of Accelerated Aging in a Mouse Model [J].
Cai, Nanshuo ;
Wu, Yifan ;
Huang, Yan .
CELLS, 2022, 11 (09)
[6]   Genome-Wide Gene Expression in relation to Age in Large Laboratory Cohorts of Drosophila melanogaster [J].
Carlson, Kimberly A. ;
Gardner, Kylee ;
Pashaj, Anjeza ;
Carlson, Darby J. ;
Yu, Fang ;
Eudy, James D. ;
Zhang, Chi ;
Harshman, Lawrence G. .
GENETICS RESEARCH INTERNATIONAL, 2015, 2015
[7]   The Genomic Basis of Postponed Senescence in Drosophila melanogaster [J].
Carnes, Megan Ulmer ;
Campbell, Terry ;
Huang, Wen ;
Butler, Daniel G. ;
Carbone, Mary Anna ;
Duncan, Laura H. ;
Harbajan, Sasha V. ;
King, Edward M. ;
Peterson, Kara R. ;
Weitzel, Alexander ;
Zhou, Shanshan ;
Mackay, Trudy F. C. .
PLOS ONE, 2015, 10 (09)
[8]   Mitochondrial encephalomyopathy in Drosophila [J].
Celotto, AM ;
Frank, AC ;
McGrath, SW ;
Fergestad, T ;
Van Voorhies, WA ;
Buttle, KF ;
Mannella, CA ;
Palladino, MJ .
JOURNAL OF NEUROSCIENCE, 2006, 26 (03) :810-820
[9]   Hidden genetic variation shapes the structure of functional elements in Drosophila [J].
Chakraborty, Mahul ;
VanKuren, Nicholas W. ;
Zhao, Roy ;
Zhang, Xinwen ;
Kalsow, Shannon ;
Emerson, J. J. .
NATURE GENETICS, 2018, 50 (01) :20-+
[10]   Caloric Restriction and Rapamycin Differentially Alter Energy Metabolism in Yeast [J].
Choi, Kyung-Mi ;
Hong, Seok-Jin ;
van Deursen, Jan M. ;
Kim, Sooah ;
Kim, Kyoung Heon ;
Lee, Cheol-Koo .
JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2018, 73 (01) :29-38