Jove
Visualize
Contact Us

Related Concept Videos

Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

10.1K
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...
10.1K
Mitochondria01:37

Mitochondria

21.4K
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,...
21.4K
Replication in Eukaryotes01:29

Replication in Eukaryotes

19.2K
In eukaryotic cells, DNA replication is highly conserved and tightly regulated. Multiple linear chromosomes must be duplicated with high fidelity before cell division, so there are many proteins that fulfill specialized roles in the replication process. Replication occurs in three phases: initiation, elongation, and termination, and ends with two complete sets of chromosomes in the nucleus.
Many Proteins Orchestrate Replication at the Origin
Eukaryotic replication follows many of the same...
19.2K
Replicative Cell Senescence02:15

Replicative Cell Senescence

4.6K
Replicative cell senescence is a property of cells that allows them to divide a finite number of times throughout the organism's lifespan while preventing excessive proliferation. Replicative senescence is associated with the gradual loss of the telomere — short, repetitive DNA sequences found at the end of the chromosomes. Telomeres are bound by a group of proteins to form a protective cap on the ends of chromosomes. Embryonic stem cells express telomerase — an enzyme that adds...
4.6K
ATP Synthase: Mechanism01:48

ATP Synthase: Mechanism

18.9K
In animals, the mitochondrial F1F0 ATP synthase is the key protein that synthesizes ATP molecules through a complex catalytic mechanism. While the nuclear genome encodes the majority of ATP synthase subunits, the mitochondrial genome encodes some of the enzyme's most critical components. The formation of this multi-subunit enzyme is a complex multi-step process regulated at the level of transcription, translation, and assembly. Defects in one or more of these steps can result in decreased...
18.9K
Meiosis I03:09

Meiosis I

46.7K
Meiosis is the division of a diploid cell into haploid cells forming sperm and eggs in animals through differentiation. Meiosis I is the first stage of meiosis, where the genetic recombination of homologous chromosomes and the reduction of the ploidy level by half occurs.
Prophase I is the most extended and complex step of meiosis I characterized by synapsis, chromosome pairing, and recombination of the homologous chromosomes. This process is facilitated by a proteinaceous structure called the...
46.7K

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Clinical Manifestations and Genetic Findings in Three Patients with Chediak-Higashi Syndrome: Highlighting the Splice Site Variants.

Iranian journal of allergy, asthma, and immunology·2026
Same author

Stress granules and tau pathology in Alzheimer's disease: A scoping review of bidirectional interactions, liquid-liquid phase separation, and proteostatic consequences.

Brain research bulletin·2026
Same author

Personalizing sinus surgery: a systematic review and meta-analysis of clinical and genetic predictors of outcome in chronic rhinosinusitis.

Journal of the Korean Association of Oral and Maxillofacial Surgeons·2026
Same author

A Cohort Study of 38 Classic Wiskott-Aldrich Syndrome Cases with Six Novel Mutations.

Journal of clinical immunology·2026
Same author

Efficacy and Safety of Pegfilgrastim in Patients With Severe Congenital Neutropenia.

EJHaem·2025
Same author

miR-361-5p contributes to the pathogenesis of Alzheimer's disease.

Scientific reports·2025
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Apr 7, 2026

Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction
09:15

Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction

Published on: July 12, 2022

5.7K

Age-related decrease in mtDNA content as a consequence of mtDNA 4977 bp deletion.

Leila Zabihi Diba1, Seyed Mojtaba Mohaddes Ardebili1, Jalal Gharesouran1

  • 1a Department of Biochemistry and Clinical Laboratory , Division of Medical Genetics, Faculty of Medicine, Tabriz University of Medical Sciences , Tabriz , Iran and.

Mitochondrial DNA. Part A, DNA Mapping, Sequencing, and Analysis
|July 9, 2015
PubMed
Summary

The common 4977 bp deletion in mitochondrial DNA accumulates with age. This study found significant differences in mitochondrial content between aged and young individuals, with deletions ranging from 2% to 17% in older adults.

Keywords:
Agingcommon deletionmitochondriamtDNA deletionΔmtDNA 4977 bp

More Related Videos

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase COX/SDH Double-labeling Histochemistry
06:53

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase COX/SDH Double-labeling Histochemistry

Published on: November 23, 2011

37.9K
Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing
07:24

Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing

Published on: February 10, 2023

2.1K

Related Experiment Videos

Last Updated: Apr 7, 2026

Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction
09:15

Measuring Single-Cell Mitochondrial DNA Copy Number and Heteroplasmy Using Digital Droplet Polymerase Chain Reaction

Published on: July 12, 2022

5.7K
Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase COX/SDH Double-labeling Histochemistry
06:53

Visualization of Mitochondrial Respiratory Function using Cytochrome C Oxidase / Succinate Dehydrogenase COX/SDH Double-labeling Histochemistry

Published on: November 23, 2011

37.9K
Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing
07:24

Genotyping Single Nucleotide Polymorphisms in the Mitochondrial Genome by Pyrosequencing

Published on: February 10, 2023

2.1K

Area of Science:

  • Gerontology
  • Molecular Biology
  • Genetics

Background:

  • The 4977 bp deletion is a frequent somatic mutation in human mitochondrial DNA (mtDNA) associated with aging.
  • Previous research on the age-dependent increase of this deletion in blood has yielded conflicting results.

Purpose of the Study:

  • To investigate the prevalence and levels of the common 4977 bp deletion in the mtDNA of elderly individuals.
  • To compare mitochondrial DNA content and deletion levels between aged and younger populations.

Main Methods:

  • Analysis of whole blood samples from 100 individuals aged 60-90 years.
  • Quantification of the common deletion and overall mtDNA deletion levels.

Main Results:

  • The common 4977 bp deletion was detected in 46% of the elderly individuals studied.
  • A statistically significant difference in mitochondrial content was observed between aged and young individuals (p=0.01).
  • Detected deletion levels varied from 2% to 17% of total mtDNA, with a mean of 10% ± 0.02%.

Conclusions:

  • The common deletion appears to decrease mtDNA content in elderly individuals.
  • The 4977 bp deletion is less consistently detectable in blood, a rapidly replicating tissue, compared to tissues with lower mitotic activity.