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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,...
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...
Mitochondrial Membranes01:45

Mitochondrial Membranes

A single mitochondrion is a bean-shaped organelle enclosed by a double-membrane system. The outer membrane of mitochondria is smooth and contains many porins - the integral membrane transporters. Porins enable free diffusion of ions and small uncharged molecules through the outer mitochondrial membrane but limit the transport of molecules larger than 5000 Daltons. Further, the outer mitochondrial membrane forms a unique structure called membrane contact sites with other subcellular organelles,...
Electron Transport Chain: Complex I and II01:46

Electron Transport Chain: Complex I and II

The mitochondrial electron transport chain (ETC) is the main energy generation system in the eukaryotic cells. However, mitochondria also produce cytotoxic reactive oxygen species (ROS) due to the large electron flow during oxidative phosphorylation. While Complex I is one of the primary sources of superoxide radicals, ROS production by Complex II is uncommon and may only be observed in cancer cells with mutated complexes.
ROS generation is regulated and maintained at moderate levels necessary...
The Effect of Aging on Tissues01:19

The Effect of Aging on Tissues

Several body functions deteriorate with age. The external signs of aging are easily identifiable. For example, the skin becomes dry, less elastic, and thins out, forming wrinkles. The skin of the face begins to appear looser due to a decrease in the levels of elastic and collagen fibers in the connective tissue. Additionally, melanin production in the hair follicle decreases with age, resulting in gray hair. Moreover, the senses of sight and hearing decline, so glasses and hearing aids may...
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:
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Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase (COX/SDH) Double-labeling Histochemistry
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Mitochondrial DNA alterations in aging.

Kamile Oztürk1, Abdullah Olgun, Ercan Saruhan

  • 1Department of Biochemistry and Clinical Biochemistry, Gülhane School of Medicine, 06018 Etlik, Ankara, Turkey. kamileztrk@yahoo.com.tr

Annals of the New York Academy of Sciences
|April 27, 2007
PubMed
Summary

Mitochondrial DNA (mtDNA) deletions did not increase with aging in a 2.4-kb region. Further sequencing is needed to detect age-dependent changes in mitochondrial DNA alterations.

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Area of Science:

  • Genetics
  • Molecular Biology
  • Aging Research

Background:

  • Mitochondrial DNA (mtDNA) alterations are associated with aging.
  • Investigating specific mtDNA regions can reveal age-related changes.

Purpose of the Study:

  • To investigate deletions/insertions in a 2.4-kb region of mtDNA, including the D-loop, in relation to aging.
  • To determine if major mtDNA deletions increase with age.

Main Methods:

  • Screened 96 individuals aged 20-94 years.
  • Purified genomic DNA from whole blood.
  • Amplified the 2.4-kb mtDNA region using PCR and visualized via agarose gel electrophoresis.
  • Sequenced one amplicon for confirmation.

Main Results:

  • Detected mtDNA deletions in only two younger individuals (ages 26 and 30) at this resolution.
  • No significant increase in major deletions/insertions was observed in the analyzed mtDNA region with aging.

Conclusions:

  • The analyzed 2.4-kb mtDNA region does not show an age-dependent increase in major deletions/insertions.
  • Complete sequencing of this mtDNA region is necessary to identify potential age-related changes.