Veneridae is a diverse, commercially important, and cosmopolitan family. Here we present the complete mitochondrial genome of the clam Meretrix petechialis (Bivalvia: Veneridae). The genome is 19,567 bp in length, and contains 36 genes including 12 protein-coding genes, two ribosomal RNAs, and 22 transfer RNAs (tRNAs). All genes are encoded on the same strand. In contrast to the typical animal mitochondrial genomes, it lacks the protein-coding gene atp8. The other distinct features of the mitochondrial genome are that it has only one copy of trnS and a duplication of the trnQ gene. Mitochondrial gene orders are most highly rearranged in the class Bivalvia. Comparing the gene arrangements between M. petechialis and Venerupis philippinarum, we observe that they share four completely identical gene blocks, two large gene blocks cox1-L1-nad1-nad2-nad4L-I and cox2-P-cytb-rrnL-nad4-H-E-S2-atp6-nad3-nad5, and two small gene blocks containing tRNA genes only. After excluding tRNAs from the comparison, the gene arrangements between M. petechialis and V. philippinarum are the same except for translocations of the genes rrnS and cox3. We also present comparisons of gene arrangements between other molluscan species.
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http://dx.doi.org/10.1080/19401730902964425 | DOI Listing |
J Gerontol A Biol Sci Med Sci
January 2025
Department of Joint Surgery, HongHui Hospital, Xi'an Jiaotong University, Xi'an, Shaanxi, China.
Background: Mitochondrial dysfunction has been demonstrated to be an important hallmark of sarcopenia, yet its specific mechanism remains obscure. In this study, mitochondrial-related genes were used as instrumental variables to proxy for mitochondrial dysfunction, and summary data for sarcopenia-related traits were used as outcomes to examine their genetic association.
Methods: A total of 1,136 mitochondrial-related genes from the human MitoCarta3.
Nat Med
January 2025
Department of Human Genetics, Radboud University Medical Center, Nijmegen, the Netherlands.
Genetic diagnosis of rare diseases requires accurate identification and interpretation of genomic variants. Clinical and molecular scientists from 37 expert centers across Europe created the Solve-Rare Diseases Consortium (Solve-RD) resource, encompassing clinical, pedigree and genomic rare-disease data (94.5% exomes, 5.
View Article and Find Full Text PDFCancer Med
January 2025
Department of Respiratory Medicine, The Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, People's Republic of China.
Background: Lung adenocarcinoma (LUAD) exhibits molecular heterogeneity, with mitochondrial damage affecting progression. The relationship between mitochondrial damage and immune infiltration, and Weighted Gene Co-expression Network Analysis (WGCNA)-derived biomarkers for LUAD classification and prognosis, remains unexplored.
Aims: The objective of our research is to identify gene modules closely related to the clinical stages of LUAD using the WGCNA method.
Wellcome Open Res
November 2024
UK Centre for Ecology & Hydrology, Wallingford, England, UK.
We present a genome assembly from an individual male (Poplar Grey moth; Arthropoda; Insecta; Lepidoptera; Noctuidae). The genome sequence has a total length of 424.20 megabases.
View Article and Find Full Text PDFGenet Med Open
March 2024
Department of Pathology, Stanford University, Stanford, CA.
The number of human disease genes has dramatically increased over the past decade, largely fueled by ongoing advances in sequencing technologies. In parallel, the number of available clinical genetic tests has also increased, including the utilization of exome sequencing for undiagnosed diseases. Although most clinical sequencing tests have been centered on enrichment-based multigene panels and exome sequencing, the continued improvements in performance and throughput of genome sequencing suggest that this technology is emerging as a potential platform for routine clinical genetic testing.
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