Common and unique transcriptional responses to dietary restriction and loss of insulin receptor substrate 1 (IRS1) in mice

• DOI: 10.18632/aging.101446
• Publication Date: 2018-05-20T20:02:20Z
• Authors: Melissa M. Page; Eugene F. Schuster; Manikhandan Mudaliar; Pawel Herzyk; Dominic J. Withers; Colin Selman
• Keywords: 570; Geriatrics & Gerontology; Transcription, Genetic; Knockout; Longevity; 610; METHIONINE RESTRICTION; LONG-LIVED MICE; transcriptomics; Mice; 03 medical and health sciences; Genetic; TERM CALORIC RESTRICTION; MODEL ORGANISMS; Animals; LIFE-SPAN EXTENSION; GENE-EXPRESSION; Caloric Restriction; Mice, Knockout; 0303 health sciences; Science & Technology; insulin receptor substrate 1; INHIBIT TRANSLATION; dietary restriction; Cell Biology; insulin/IGF-1 signalling; C-ELEGANS; Insulin Receptor Substrate Proteins; SKELETAL-MUSCLE; CAENORHABDITIS-ELEGANS; Transcription; Life Sciences & Biomedicine; lifespan; Developmental Biology; Research Paper

Dietary restriction (DR) is the most widely studied non-genetic intervention capable of extending lifespan across multiple taxa. Modulation of genes, primarily within the insulin/insulin-like growth factor signalling (IIS) and the mechanistic target of rapamycin (mTOR) signalling pathways also act to extend lifespan in model organisms. For example, mice lacking insulin receptor substrate-1 (IRS1) are long-lived and protected against several age-associated pathologies. However, it remains unclear how these particular interventions act mechanistically to produce their beneficial effects. Here, we investigated transcriptional responses in wild-type and IRS1 null mice fed an ad libitum diet (WTAL and KOAL) or fed a 30% DR diet (WTDR or KODR). Using an RNAseq approach we noted a high correlation coefficient of differentially expressed genes existed within the same tissue across WTDR and KOAL mice and many metabolic features were shared between these mice. Overall, we report that significant overlap exists in the tissue-specific transcriptional response between long-lived DR mice and IRS1 null mice. However, there was evidence of disconnect between transcriptional signatures and certain phenotypic measures between KOAL and KODR, in that additive effects on body mass were observed but at the transcriptional level DR induced a unique set of genes in these already long-lived mice.