The aim of our investigation was to study the gastric mucosa DNA synthesis pattern in different experimental models of duodenal reflux. The following operations were performed on male Wistar rats: (A) sham-operation; (B) Roux-Y gastrectomy; (C) Billroth I; (D) Polya-type partial gastrectomy; (E) Billroth II; and (F) simple gastroenterostomy. Fifteen weeks later rats were sacrificed and histological and in vitro 3H thymidine autoradiographic studies were carried out. Gastric mucosal DNA synthesis rate was also estimated. Besides group A, all other groups showed variable degrees of gastritis mainly located at the anastomosis or at the gastrostomy suture line. Severe gastritis was not present in group B rats and most commonly occurred in group F rats. Group C, D, E and F showed an intense epithelial proliferation with a labeling index significantly higher than in the controls. However, mucosal DNA synthesis rate appeared to decrease with the progression of gastritis and in group F, the group more exposed to duodenal reflux, was significantly lower than in the controls. It is postulated that progressive exposure to duodenal reflux and secondary atrophic gastric changes following gastric surgery is accompanied by a reduction in the mucosal layer of the DNA synthesis rate, due to the loss of epithelial elements and the increase in connective and inflammatory elements, together with an enhanced turnover of the residual epithelial cells.
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http://dx.doi.org/10.1016/0753-3322(89)90087-5 | DOI Listing |
Methods Mol Biol
January 2025
Department of Microbiology and Plant Pathology, University of California, Riverside, CA, USA.
Transcriptional regulation allows cells to execute developmental programs, maintain homeostasis, and respond to intra- and extracellular signals. Central to these processes are promoters, which in eukaryotes are sequences upstream of genes that bind transcription factors (TFs) and which recruit RNA polymerase to initiate mRNA synthesis. Valuable tools for studying promoters include reporter genes, which can be used to indicate when and where genes are activated.
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Department of Medicinal Chemistry, University of Washington, Seattle, WA 98195, USA.
Background: Thiopurine methyltransferase (TPMT) plays a crucial role in the detoxification of thiopurine drugs, including the antimetabolites azathioprine and 6-mercaptopurine (6-MP) used to treat autoimmune diseases and various cancers. These drugs interfere with DNA synthesis by inhibiting the production of purine-containing nucleotides, leading to the death of rapidly dividing cells. TPMT inactivates thiopurine drugs by methylating at the thiol group.
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December 2024
CUHKSZ-Boyalife Regenerative Medicine Engineering Joint Laboratory, School of Medicine, The Chinese University of Hong Kong, Shenzhen 518172, China.
The Phi29 DNA polymerase is renowned for its processivity in synthesizing single-stranded DNA amplicons by rolling around a circularized DNA template. However, DNA synthesis rolling circle amplification (RCA) is significantly hindered by the secondary structure in the circular template. To overcome this limitation, an engineered circular template without secondary structure could be utilized to improve the sensitivity of RCA-based assays without increasing its complexity.
View Article and Find Full Text PDFBiosensors (Basel)
December 2024
Department of Bioscience and Biotechnology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, Republic of Korea.
We developed a rapid and sensitive diagnostic platform that integrates isothermal viral gene amplification with a nucleic acid lateral flow assay (NALFA) to detect SARS-CoV-2 RNA. Isothermal gene amplification was performed by combining reverse transcription of viral RNA with recombinase polymerase amplification (RPA). In our diagnostic platform, DNA primers for the RPA reaction were modified by appending DNA tails, enabling the synthesis of tailed amplicon DNAs.
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Gynecology and Obstetrics 1U, Department of Surgical Sciences, University of Turin, 10126 Turin, Italy.
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