We have recently identified a protein in HeLa nuclear extracts which recognises the single-stranded telomeric sequence (CCCTAA)n in vertebrates [Marsich, E., Piccini, A., Xodo, L. E. & Manzini, G. (1996) Nucleic Acids Res. 24, 4029-4033]. In this paper we provide further experimental evidence, using electrophoretic mobility shift assays, SDS/PAGE after ultraviolet cross-linking, and gel permeation chromatography techniques, that: (a) this protein displays remarkably stringent requirements for the telomeric motif sequence, as (CCCTAAA)n, (CCCCAA)n and (TCCCAA)n are tightly bound, but (CCTAA)n is not; (b) it requires at least four CCC-block repeats properly spaced to bind strongly to DNA, e.g. the polypurine stretch of the murine Ki-ras promoter d(CTCCCTCCCTCCCTCCTTCCCTCCCTCCC), the CarG-motif-containing sequence d(CCATTTCCTAATTAGGTAAAAG), and d(C)22 are not recognised by this protein; (c) it is present in nuclear extracts from several vertebrate sources including human, rat, pig, hamster and chicken; (d) its molecular mass is about 40 kDa, as determined by SDS/ PAGE and non-denaturing gel permeation chromatography, suggesting that this protein is monomeric under native conditions.
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http://dx.doi.org/10.1046/j.1432-1327.1998.2580093.x | DOI Listing |
Methods Mol Biol
March 2025
Laboratory of Entomology and Phytopathology, Molecular Plant Virology, State University of the North Fluminense Darcy Ribeiro, Rio de Janeiro, Brazil.
Members of the family Geminiviridae have single-stranded (ss), circular DNA genomes that are encapsidated into non-enveloped quasi-icosahedral twinned (geminate) particles, causing yield losses in several economically important crops worldwide. Sequence-based approaches used for molecular characterization of Geminiviridae genomes, associated with powerful bioinformatic tools, provided a better picture about the true extent of the Geminiviridae species diversity. This chapter describes procedures to reconstruct Geminiviridae phylogenetic relationships based on coat protein (CP) and replication-associated protein (Rep) amino acid sequences and full-length nucleotide genomes using both maximum likelihood (ML) and Bayesian inference (BI) approaches.
View Article and Find Full Text PDFBiomedicines
February 2025
Department of Pharmacy (DIFARMA), University of Salerno, 84084 Fisciano, SA, Italy.
Absent in melanoma 2 (AIM2) is a member of the innate immune sensors that recognizes cytosolic nucleic acids, leading to inflammasome assembly. In recent years, several studies in the oncology field have highlighted the presence of cytoplasmic double-stranded DNA (dsDNA) following necrosis and/or genomic instability, which is typical of malignant transformation. The recognition of dsDNA by the AIM2 inflammasome either in cancer cells or in immune cells can further exacerbate inflammatory processes on the basis of cancer progression.
View Article and Find Full Text PDFNucleic Acids Res
February 2025
State Key Laboratory of Cellular Stress Biology, School of Life Sciences, Faculty of Medicine and Life Sciences, Xiamen University, No. 4221, Xiang'an South Road, Xiamen 361102, China.
Short prokaryotic Argonaute and the associated TIR-APAZ (SPARTA) proteins constitute a prokaryotic immune system, mediating RNA- or DNA-guided target single-stranded DNA (ssDNA) to activate NADase activity and induce cell death by degrading NAD+ in response to invading plasmids. Although the guide RNA-mediated targeting mechanism of SPARTA has been established, the functional role and mechanisms of guide DNA-mediated SPARTA remain poorly understood. Here, we report two crystal structures of Crenotalea thermophila SPARTA complexes with 5'-phosphorylated 21-nt guide DNA and complementary target ssDNA lengths of 15 or 20 nt.
View Article and Find Full Text PDFNature
March 2025
MRC Laboratory of Molecular Biology, Cambridge, UK.
Langmuir
February 2025
Department of Chemistry and Biology, Graduate School of Science and Engineering, Ehime University, 2-5 Bunkyo, Matsuyama, Ehime 790-8577, Japan.
Gold nanoparticles (AuNPs) have been utilized as colorimetric biosensors by which target molecule-induced AuNP aggregation is recognized by a color change from red to blue. Particularly, single-stranded DNA (ssDNA)-immobilized AuNPs (ssDNA-AuNPs) have been applied to genetic diagnosis. Herein, we investigated the effect of the density of immobilized ssDNA on the sensitivity of the target ssDNA detection using two different cross-linking aggregation models of ssDNA-AuNPs, i.
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