4.6 Article

Age-Related Changes of Gene Expression Profiles in Drosophila

Journal

GENES
Volume 12, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/genes12121982

Keywords

aging processes; microarray; Drosophila; muscle structure; cytochrome

Funding

  1. National Science Foundation [MCB-1616740]
  2. Department of Defense [PC160049]

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An individual's gene expression profile changes throughout life, with differences in gene expression between young and old organisms driven by physiological needs and functions. Muscle development genes are mostly downregulated in older flies, while genes related to apoptosis and resistance to toxic chemicals are upregulated. Results also suggest potential functions of unknown genes in affecting lifespan.
An individual's gene expression profile changes throughout their life. This change in gene expression is shaped by differences in physiological needs and functions between the younger and older organism. Despite intensive studies, the aging process is not fully understood, and several genes involved in this process may remain to be identified. Here we report a transcriptomic analysis of Drosophila melanogaster using microarrays. We compared the expression profiles of two-day-old female adult flies with those of 45-day-old flies. We identified 1184 genes with pronounced differences in expression level between young and old age groups. Most genes involved in muscle development/maintenance that display different levels of expression with age were downregulated in older flies. Many of these genes contributed to sarcomere formation and function. Several of these genes were functionally related to direct and indirect flight muscles; some of them were exclusively expressed in these muscles. Conversely, several genes involved in apoptosis processes were upregulated in aging flies. In addition, several genes involved in resistance to toxic chemicals were upregulated in aging flies, which is consistent with a global upregulation of the defense response system in aging flies. Finally, we randomly selected 12 genes among 232 genes with unknown function and generated transgenic flies expressing recombinant proteins fused with GFP protein to determine their subcellular expression. We also found that the knockdown of some of those 12 genes can affect the lifespan of flies.

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