The complete mitochondrial genome of Piccinelli and Prosdocimi, 1968 (Crustacea: Anostraca).

Mitochondrial DNA B Resour

Institute of Fisheries Science, Tibet Academy of Agricultural and Animal Husbandry Sciences, Lhasa, P. R. China.

Published: March 2022

In the study, we report the complete mitochondrial genome of Piccinelli and Prosdocimi, 1968 for the first time. The mitochondrial genome of is 15,436 bp in length, with the typical structure of 13 protein-coding genes (PCGs), 22 transfer RNA genes (tRNAs) and 2 ribosomal RNA genes, and a non-coding control region (CR). Phylogenetic analysis showed that was at the basal position among the bisexual species, which revealed that is likely to be an ancestral clade. The present study could provide effective resources for population genetics study, as well as germplasm conservation in .

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8920358PMC
http://dx.doi.org/10.1080/23802359.2022.2036258DOI Listing

Publication Analysis

Top Keywords

mitochondrial genome
12
complete mitochondrial
8
genome piccinelli
8
piccinelli prosdocimi
8
prosdocimi 1968
8
rna genes
8
1968 crustacea
4
crustacea anostraca
4
anostraca study
4
study report
4

Similar Publications

Background: Tea-oil Camellia within the genus Camellia is renowned for its premium Camellia oil, often described as "Oriental olive oil". So far, only one partial mitochondrial genomes of Tea-oil Camellia have been published (no main Tea-oil Camellia cultivars), and comparative mitochondrial genomic studies of Camellia remain limited.

Results: In this study, we first reconstructed the entire mitochondrial genome of C.

View Article and Find Full Text PDF

Mitochondrial endonuclease G (EndoG) contributes to chromosomal degradation when it is released from mitochondria during apoptosis. It is presumed to also have a mitochondrial function because EndoG deficiency causes mitochondrial dysfunction. However, the mechanism by which EndoG regulates mitochondrial function is not known.

View Article and Find Full Text PDF

Background: The transfer of mitochondrial DNA into the nuclear genomes of eukaryotes (Numts) has been linked to lifespan in non-human species and recently demonstrated to occur in rare instances from one human generation to the next.

Method: Here we investigated numtogenesis dynamics in humans in two ways. First, we quantified Numts in 1,187 post-mortem brain and blood samples from different individuals.

View Article and Find Full Text PDF

Background: Mitochondria are organelles where energy production takes place via oxidative phosphorylation, thus mitochondrial function influences the organs with large energy consumption, such as the brain. Mitochondria contain their own circular genome (mtDNA), which encodes essential proteins/RNAs involved in oxidative phosphorylation. The maternal inheritance of mtDNA, combined with a higher risk of Alzheimer's disease (AD) observed in females, suggest mtDNA may have a role in AD.

View Article and Find Full Text PDF

Background: Mitochondrial dysfunction and Aβ accumulation are hallmarks of Alzheimer's disease (AD). However, the role of these pathologies in Down Syndrome associated Alzheimer's Disease (DSAD) is unknown. Decades of research describe a relationship between mitochondrial function and Aβ production.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!