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Mitochondrial divergence between slow- and fast-aging garter snakes.
Tonia S Schwartz1, Zebulun W Arendsee2, Anne M Bronikowski1
1Iowa State University, Ecology, Evolution & Organismal Biology Department, Ames, IA 50011, USA.
Experimental Gerontology
|September 26, 2015
Summary
Aging rates in garter snakes are linked to distinct mitochondrial DNA (deoxyribonucleic acid) and gene expression patterns. These genetic differences in mitochondria may explain variations in aging and lifespan between ecotypes.
Area of Science:
- Evolutionary Biology
- Genomics
- Gerontology
Background:
- Mitochondrial function is a key factor in aging, with declining efficiency and increased free radical production implicated.
- Understanding mitochondrial genotype and phenotype evolution is crucial, especially in species with adaptable physiology.
- Garter snake ecotypes offer a unique model due to divergent aging rates and lifespans despite geographical proximity.
Purpose of the Study:
- To investigate mitochondrial genome-types and transcription in garter snake ecotypes with differing aging rates.
- To identify genetic and regulatory elements within the mitochondrial genome.
- To assess divergence in mitochondrial gene expression and protein-coding regions between slow-aging (SA) and fast-aging (FA) ecotypes.
Main Methods:
- Reconstruction of the garter snake mitochondrial genome sequence using RNA-sequencing (RNA-seq) data.
- Bioinformatic identification of regulatory elements, including a glucocorticoid response element (GRE).
- Analysis of mitochondrial gene expression divergence between ecotypes and under heat stress.
- Sequencing of mitochondrial protein-coding regions to identify genetic variations.
Main Results:
- Two mitochondrial control regions were identified, one containing a GRE.
- Higher gene expression of protein-coding genes was observed in FA snakes compared to SA snakes.
- SA and FA ecotypes exhibited unique mitochondrial haplotypes with amino acid substitutions in CYTB and ND5.
- A significant CYTB amino acid change (Isoleucine to Threonine) was highly segregated between ecotypes.
Conclusions:
- Divergent mitochondrial haplotypes in SA and FA garter snake ecotypes correlate with differences in mitochondrial function.
- These genetic divergences in mitochondria, particularly in CYTB and ND5, may underlie the observed variations in aging rates.
- Mitochondrial genetic makeup plays a significant role in the evolution of aging and lifespan.
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