Gene structure of the murine 2'-5'-oligoadenylate synthetase family.

Cell Mol Life Sci

Department of Molecular and Structural Biology, University of Aarhus, Denmark.

Published: July 2002

The 2'-5'-oligoadenylate synthetases (OASs) are members of a family of interferon-induced proteins playing an important role in the antiviral effect of interferons as well as being involved in apoptosis and control of cellular growth. Based on sequence data from the murine BAC clone (RP23-39M18), and a number of EST and IMAGE clones and the Celera Mouse database, we identified twelve Oas genes in the mouse genome, all localized to the chromosome 5F region. In contrast to the single OAS1 gene found in humans, we identified eight closely linked Oas1 genes in the murine genome, together with the genes of Oas2 and Oas3. Compared to the single OASL gene found in humans, two genes of OAS-like proteins, Oasl1 and Oasl2, were identified. All the putative genes seem to be transcribed. The exon/intron structures of the murine Oas genes were found to be identical to those of the human genes.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11337553PMC
http://dx.doi.org/10.1007/s00018-002-8499-2DOI Listing

Publication Analysis

Top Keywords

oas genes
8
gene humans
8
genes
7
gene structure
4
murine
4
structure murine
4
murine 2'-5'-oligoadenylate
4
2'-5'-oligoadenylate synthetase
4
synthetase family
4
family 2'-5'-oligoadenylate
4

Similar Publications

This review highlights the sulfur transporters, key enzymes and their encoding genes involved in plant sulfur anabolism, focusing on their occurrence, chemistry, location, function, and regulation within sulfur assimilation pathways. Sulfur, a vital element for plant life, plays diverse roles in metabolism and stress response. This review provides a comprehensive overview of the sulfur assimilation pathway in plants, highlighting the intricate network of enzymes and their regulatory mechanisms.

View Article and Find Full Text PDF
Article Synopsis
  • Hematologic malignancies significantly impact the health of children, young adults, and older adults, yet their biological causes are not well understood.
  • A study revealed notable differences in clinical features and genomic mutations between children/young adults (CYAs) and older adults (OAs) in these diseases, including lower mutational burdens in CYAs for many key genes.
  • The research identified specific genes with varying mutation rates and emphasized the need for age-oriented personalized treatment options based on the distinct genetic and clinical landscapes of CYAs and OAs.
View Article and Find Full Text PDF

Background: Breast cancer is the most common malignancy among women worldwide, characterized by complex molecular and cellular heterogeneity. Despite advances in diagnosis and treatment, there is an urgent need to identify reliable biomarkers and therapeutic targets to improve early detection and personalized therapy. The OAS (2'-5'-oligoadenylate synthetase) family genes, known for their roles in antiviral immunity, have emerged as potential regulators in cancer biology.

View Article and Find Full Text PDF

Biofortifying multiple micronutrients and decreasing arsenic accumulation in rice grain simultaneously by expressing a mutant allele of OAS-TL gene.

New Phytol

December 2024

State Key Laboratory of Crop Genetics & Germplasm Enhancement and Utilization, College of Resources and Environmental Sciences, Nanjing Agricultural University, Nanjing, 210095, China.

Article Synopsis
  • Rice grains often have high arsenic levels and low essential nutrients, which can impact human health and nutrition.
  • Researchers created genetically modified rice that expresses a mutant gene (astol1) to boost cysteine production and reduce arsenic accumulation.
  • This modified rice showed increased essential nutrient levels and improved arsenic tolerance, suggesting a promising approach to both enhance nutrition and decrease toxicity in rice.
View Article and Find Full Text PDF

PU.1 regulates osteoarthritis progression via CSF1R in synovial cells.

Biochim Biophys Acta Mol Basis Dis

January 2025

Department of Oncology, Shengjing Hospital of China Medical University, Shenyang 110001, PR China. Electronic address:

This study elucidates the molecular mechanisms driving osteoarthritis (OA) by focusing on the transcription factor PU.1's role in synovial cells, specifically macrophages and fibroblast-like synoviocytes (FLS). Analyzing OA-related synovial gene expression from the GEO database highlighted immune regulation pathways in OA.

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!