Jove
Visualize
Contact Us
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 Concept Videos

Animal Mitochondrial Genetics02:59

Animal Mitochondrial Genetics

7.4K
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...
7.4K
Mismatch Repair01:20

Mismatch Repair

4.8K
Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
The Mutator Protein Family Plays a Key Role in DNA Mismatch Repair
The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
4.8K
RNA Editing02:23

RNA Editing

8.9K
RNA editing is a post-transcriptional modification where a precursor mRNA (pre-mRNA) nucleotide sequence is changed by base insertion, deletion, or modification. The extent of RNA editing varies from a few hundred bases, in mitochondrial DNA of trypanosomes, to a just single base, in nuclear genes of mammals. Even a single base change in the pre-mRNA can convert a codon for one amino acid into the codon for another amino acid or a stop codon. This type of re-coding can significantly affect the...
8.9K

You might also read

Related Articles

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

Sort by
Same author

Identification of breakpoint regions and single nucleotide variations of RHD hybrid alleles by long-read sequencing.

Vox sanguinis·2026
Same author

Alternative organelle targeting of OPA1 mediates fatty acid release from lipid droplets.

bioRxiv : the preprint server for biology·2026
Same author

High-resolution single-cell mapping of clonal hematopoiesis and structural variation in aplastic anemia.

Nature genetics·2026
Same author

A Conserved Enhancer Locus in Extrachromosomal DNA and Homogeneously Staining Regions Activates MYC Transcription in Group 3 Medulloblastoma.

Cancer research·2026
Same author

MitoEdit: A pipeline for optimizing mtDNA base editing and predicting bystander effects.

Computational and structural biotechnology journal·2026
Same author

Developmental reprogramming underlies chemotherapy resistance in favorable-histology Wilms tumor.

Cell reports·2026
Same journal

A human-specific genetic modifier reconfigures large-scale cortical network dynamics underlying behavioral performance.

bioRxiv : the preprint server for biology·2026
Same journal

<i>Staphylococcus aureus</i> uses a eukaryotic-like uridyltransferase to make UDP-GlcNAc for cell wall synthesis.

bioRxiv : the preprint server for biology·2026
Same journal

Dynamic redistribution of eIF4F controls cap-dependent translation initiation.

bioRxiv : the preprint server for biology·2026
Same journal

When does additional information improve accuracy of RNA secondary structure prediction?

bioRxiv : the preprint server for biology·2026
Same journal

Normative brain-state trajectories reveal deviation from healthy aging in Alzheimer's disease.

bioRxiv : the preprint server for biology·2026
Same journal

Noradrenergic infraslow rhythm during sleep is the critical link between heart-rate dynamics and memory consolidation.

bioRxiv : the preprint server for biology·2026
See all related articles

Related Experiment Video

Updated: May 29, 2025

Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors
09:22

Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors

Published on: February 28, 2021

5.4K

MitoEdit: a pipeline for optimizing mtDNA base editing and predicting bystander effects.

Devansh Shah, Kelly McCastlain, Ti-Cheng Chang

    Biorxiv : the Preprint Server for Biology
    |February 3, 2025
    PubMed
    Summary
    This summary is machine-generated.

    MitoEdit is a new tool that predicts unintended edits in mitochondrial DNA (mtDNA) base editing, streamlining research on mtDNA mutations and associated diseases.

    More Related Videos

    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

    1.4K
    A Nonsequencing Approach for the Rapid Detection of RNA Editing
    08:50

    A Nonsequencing Approach for the Rapid Detection of RNA Editing

    Published on: April 21, 2022

    2.5K

    Related Experiment Videos

    Last Updated: May 29, 2025

    Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors
    09:22

    Functional Assessment of BRCA1 variants using CRISPR-Mediated Base Editors

    Published on: February 28, 2021

    5.4K
    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

    1.4K
    A Nonsequencing Approach for the Rapid Detection of RNA Editing
    08:50

    A Nonsequencing Approach for the Rapid Detection of RNA Editing

    Published on: April 21, 2022

    2.5K

    Area of Science:

    • Genomics
    • Molecular Biology
    • Bioinformatics

    Background:

    • Mitochondrial DNA (mtDNA) mutations are linked to inherited respiratory disorders.
    • The role of somatic mtDNA mutations in chronic diseases and cancer requires further investigation.
    • Current mtDNA base editing tools face challenges with predicting unintended 'bystander' edits.

    Purpose of the Study:

    • To develop a computational tool for predicting bystander edits in mtDNA base editing.
    • To optimize the identification of target windows for mtDNA mutation studies.
    • To reduce experimental trial-and-error in mtDNA base editing construct development.

    Main Methods:

    • Developed MitoEdit, a novel computational tool for mtDNA base editing.
    • MitoEdit analyzes DNA sequences to predict potential bystander edits and their functional impact.
    • The tool incorporates empirical base editor patterns and TALE-binding sequences.

    Main Results:

    • MitoEdit accurately predicts the majority of bystander edits in silico.
    • The tool identifies optimal target windows and reduces the need for empirical testing.
    • MitoEdit automates the prediction of base edits in mitochondrial DNA.

    Conclusions:

    • MitoEdit represents the first automated tool for predicting base edits in mitochondrial DNA.
    • This tool can accelerate research into mtDNA mutations and their role in disease.
    • MitoEdit is freely available to the scientific community.