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Increasing evidence suggests that overlapping genes are much more common in eukaryotic genomes than previously thought. These different-strand overlapping genes are potential sense-antisense (SAS) pairs, which might have regulatory effects on each other. In the present study, we identified the SAS loci in the equine genome using previously generated stranded, paired-end RNA sequencing data from the equine chorioallantois. We identified a total of 1261 overlapping loci. The ratio of the number of overlapping regions to chromosomal length was numerically higher on chromosome 11 followed by chromosomes 13 and 12. These results show that overlapping transcription is distributed throughout the equine genome, but that distributions differ for each chromosome. Next, we evaluated the expression patterns of SAS pairs during the course of gestation. The sense and antisense genes showed an overall positive correlation between the sense and antisense pairs. We further provide a list of SAS pairs with both positive and negative correlation in their expression patterns throughout gestation. This study characterizes the landscape of sense and antisense gene expression in the placenta for the first time and provides a resource that will enable researchers to elucidate the mechanisms of sense/antisense regulation during pregnancy.
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http://dx.doi.org/10.3390/genes10070503 | DOI Listing |
JMIR Res Protoc
September 2025
Department of Psychiatry, Samsung Medical Center, School of Medicine, Sungkyunkwan University, Seoul, Republic of Korea.
Background: Autism spectrum disorder (ASD) and social communication disorder (SCD) are neurodevelopmental disorders characterized by deficits in social communication that hinder social adaptation, with limited pharmacological options for therapy owing to the absence of identified biomarkers. Individuals with ASD or SCD require lifelong interventions tailored to their development stages. However, most existing interventions primarily focus on early childhood, leaving adolescents relatively underserved.
View Article and Find Full Text PDFBone Jt Open
September 2025
Sydney Knee Specialists, Kogarah, Australia.
Aims: Regardless of one's alignment philosophy and belief in ligament releases, the precise estimation of soft-tissue laxities is crucial in total knee arthroplasty (TKA). This study prospectively assessed the reliability of surgeons' and assistants' measurements of ligament tension during robotic arm-assisted TKA.
Methods: A prospective, surgeon-blinded study was performed in 123 patients undergoing TKA by six surgeon/assistant pairs.
Comput Med Imaging Graph
August 2025
Nantes Université, École Centrale Nantes, CNRS, LS2N, UMR 6004, 1 Rue de la Noë, Nantes, 44000, France. Electronic address:
Medical imaging techniques like mammography enable early breast cancer detection and are part of regular screening programs. Typically, a mammogram exam involves two views of each breast, providing complementary information, but physicians rate the breast as a whole. Computer-Aided Diagnostic tools focus on detecting lesions in a single view, which is challenging due to high image resolution and varying scales of abnormalities.
View Article and Find Full Text PDFMol Nutr Food Res
September 2025
Department of Translational Genomics, GROW - Research Institute For Oncology and Reproduction, Maastricht University, Maastricht, the Netherlands.
A diet rich in fruits and vegetables (F&Vs) reduces chronic disease risk by modulating oxidative stress, inflammatory cytokines, and immune cell activity in the blood. Given the complexity of peripheral blood and its cellular components, understanding cell-type-specific responses to F&V interventions remains essential and challenging. We used CIBERSORTx to analyze immune cell fractions and gene expression profiles from RNA sequencing data of the MiBLEND study, which assessed the impact of seven F&V blends on chronic disease markers, phytochemical absorption, and gene expression changes in blood.
View Article and Find Full Text PDFInt J Stroke
August 2025
Department of Genetics and Genomics, Rajendra Institute of Medical Sciences, Ranchi, Jharkhand, INDIA.
IntroductionCerebrovascular diseases (CeVD) and neurodegenerative diseases (ND) are two major neurological disorders, which are associated with increasing global morbidity and mortality. Population-based studies have indicated a complex link between CeVD and ND. However, the shared genetic etiology between these disease conditions remains less explored.
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