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Related Concept Videos

Mitochondria01:37

Mitochondria

Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
Mitochondria01:37

Mitochondria

Mitochondria are eukaryotic cellular organelles that are known to produce energy through a process called oxidative phosphorylation. Besides their primary function, mitochondria are involved in various cellular processes, including cell growth, differentiation, signaling, metabolism, and senescence. Age-related changes cause a decline in mitochondrial quality and integrity due to increased mitochondrial mutations and oxidative damage. Thus, aging can severely impact mitochondrial functions,...
Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

Among all the organelles in an animal cell, only mitochondria have their own independent genomes. Animal mitochondrial DNA is a double-stranded, closed-circular molecule with around 20,000 base pairs. Mitochondrial DNA is unique in that one of its two strands, the heavy, or H, -strand is guanine rich, whereas the complementary strand is cytosine rich and called the light, or L, -strand. Compared to nuclear DNA, mitochondrial DNA has a very low percentage of non-coding regions and is marked by...
Export of Mitochondrial and Chloroplast Genes02:19

Export of Mitochondrial and Chloroplast Genes

A eukaryotic cell can have up to three different types of genetic systems: nuclear, mitochondrial, and chloroplast. During evolution, organelles have exported many genes to the nucleus; this transfer is still ongoing in some plant species. Approximately 18% of the Arabidopsis thaliana nuclear genome is thought to be derived from the chloroplast’s cyanobacterial ancestor, and around 75% of the yeast genome derived from the mitochondria’s bacterial ancestor. This export has occurred irrespective...
Mitochondrial Precursor Proteins01:39

Mitochondrial Precursor Proteins

Mitochondrial precursors are partially unfolded or loosely folded polypeptide chains. Newly synthesized precursors are inhibited from spontaneously folding into their native conformation by the cytosolic chaperones, heat shock proteins 70 (Hsp70), and mitochondrial import stimulation factors (MSFs). Precursors bound to MSFs are guided to the TOM70-TOM37 receptors, while precursors bound to Hsp70  chaperones are targetted to TOM20-TOM22 receptor complexes.
Most of the mitochondrial precursors...
Translocation of Proteins into the Mitochondria01:19

Translocation of Proteins into the Mitochondria

Mitochondrial precursors are translocated to the internal subcompartments via independent mechanisms involving distinct protein machineries called translocases.
Sorting of outer membrane proteins:
Mitochondrial outer membrane proteins are of two types: the transmembrane, beta-barrel porins, and the membrane-anchored, alpha-helical proteins. Beta-barrel porin precursors are translocated by the TOM complex and inserted into the outer mitochondrial membrane by the SAM complex. In contrast,...

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Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry
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Mitochondriogenesis genes and extreme longevity.

Catalina Santiago1, Nuria Garatachea, Thomas Yvert

  • 1Universidad Europea de Madrid, Madrid, Spain.

Rejuvenation Research
|November 29, 2012
PubMed
Summary
This summary is machine-generated.

Genetic variants in the PPARD-PPARGC1A-NRF-TFAM pathway generally do not influence extreme longevity. However, a potential marginal association was observed for a specific polymorphism, rs1937, in centenarians.

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Area of Science:

  • Genetics
  • Molecular Biology
  • Gerontology

Background:

  • The proliferator-activated receptor delta (PPARD)-peroxisome proliferator-activated receptor γ coactivator 1α (PPARGC1A, PGC1-α)-nuclear respiratory factor (NRF)-mitochondrial transcription Factor A (TFAM) pathway is crucial for mitochondriogenesis.
  • This pathway influences various health and disease phenotypes.
  • Its association with extreme longevity remains unexplored.

Purpose of the Study:

  • To investigate the association between common polymorphisms in the PPARD-PPARGC1A-NRF-TFAM pathway and extreme longevity.
  • To determine if genetic variations in this mitochondriogenesis pathway contribute to exceptional lifespan.

Main Methods:

  • A case-control study design was employed.
  • The study included 107 centenarians (cases) and 284 young adults (controls).
  • Five common polymorphisms (rs2267668, rs8192678, rs6949152, rs12594956, rs1937) within the pathway genes were analyzed for allele and genotype frequencies.

Main Results:

  • No significant differences in allele or genotype frequencies were found between centenarians and controls for most studied polymorphisms.
  • A statistically significant difference (p=0.003) was observed for the CC genotype in rs1937, present in 2.8% of centenarians but absent in controls.
  • This finding suggests a potential, albeit marginal, association for rs1937 with extreme longevity.

Conclusions:

  • The common genetic variants within the PPARD-PPARGC1A-NRF-TFAM pathway are generally not associated with extreme longevity.
  • A possible marginal association exists for the rs1937 polymorphism, warranting further investigation.
  • This study contributes to understanding the genetic underpinnings of exceptional lifespan.