Down regulation of gyrase A gene expression in E. coli by antisense ribozymes using RT-PCR

2007 ◽  
Vol 35 (4) ◽  
pp. 575-578 ◽  
Author(s):  
Shilpakala Sainath Rao ◽  
H. S. Savithri ◽  
Malathi Raghunathan
2001 ◽  
Vol 170 (3) ◽  
pp. 555-564 ◽  
Author(s):  
AR Green ◽  
EL Parrott ◽  
M Butterworth ◽  
PS Jones ◽  
P Greaves ◽  
...  

This study compares the actions of oestradiol, tamoxifen, toremifene and raloxifene on enzyme and gene expression in uterine tissues of ovariectomised rats over 72 h. The time-course for the induction of ornithine decarboxylase by the compounds showed a rapid biphasic response, while for creatine kinase brain type (BB) there was a continued increase over 72 h. The efficacy of induction showed that, with both markers, oestradiol gave the highest induction level, followed by tamoxifen or toremifene and then raloxifene. RT-PCR demonstrated that all compounds decreased oestrogen receptor (ER) alpha, ERbeta and ERbeta2 gene expression, 8-24 h after the first dose, suggesting that down-regulation of ER is not the primary cause of the difference in efficacy between these compounds. Using cDNA arrays, expression of 512 genes was examined in the uteri of oestradiol- or tamoxifen-treated rats. Both compounds resulted in the up-regulation of heat-shock protein 27, telomerase-associated protein 1 and secretin. However, most surprising was the marked down-regulation of Wilms' tumour and retinoblastoma genes. We speculate that this may result in a loss of regulation of the transition from the G1 to the S phase in the cell cycle and may make cells more vulnerable to the carcinogenic effects of tamoxifen in this tissue.


1998 ◽  
Vol 66 (8) ◽  
pp. 3952-3958 ◽  
Author(s):  
Silvia Ragno ◽  
Iris Estrada-Garcia ◽  
Robert Butler ◽  
M. Joseph Colston

ABSTRACT We have investigated changes in gene expression in mouse peritoneal macrophages following infection with virulent Mycobacterium tuberculosis. Using differential-display reverse transcription-PCR (RT-PCR), we have identified a gene that was markedly down-regulated within 6 h of infection and remained so for the duration of the experiment (5 days). On sequencing, this gene was found to encode the murine cytochrome c oxidase subunit VIIc (COX VIIc). Down-regulation of COX VIIc during M. tuberculosisinfection was confirmed by three independent techniques: limiting-dilution RT-PCR, RNase protection assay, and Northern analysis. Limiting-dilution RT-PCR and Northern analysis were also used to analyze the specificity of this regulation; heat-killed M. tuberculosis, Mycobacterium bovis BCG, and latex beads had no effect on expression of COX VIIc. Down-regulation of this enzyme was also confirmed by using adherent cells isolated from spleens of M. tuberculosis-infected mice. These ex vivo macrophages showed apoptotic features, suggesting a possible involvement of cytochrome c oxidase in the programmed cell death of the host cells.


2004 ◽  
Vol 72 (4) ◽  
pp. 2358-2368 ◽  
Author(s):  
Nayoung Kim ◽  
Elizabeth A. Marcus ◽  
Yi Wen ◽  
David L. Weeks ◽  
David R. Scott ◽  
...  

ABSTRACT Reciprocal interactions between Helicobacter pylori and cells of the gastric epithelium to which it adheres may affect colonization. Changes in gene expression of H. pylori induced by adhesion to AGS gastric cancer cells by coculture were compared to changes in gene expression of H. pylori cultured without AGS cells by using cDNA filter macroarrays. Adhesion was quantitatively verified by confocal microscopy of green fluorescent protein-expressing bacteria. Four experiments showed that 22 and 21 H. pylori genes were consistently up- and down-regulated, respectively. The up-regulated genes included pathogenicity island, motility, outer membrane protein, and translational genes. The σ28 factor antagonist flgM, flgG, the stress response gene, flaA, omp11, and the superoxide dismutase gene (sodB) were down-regulated. The up-regulation of cag3, flgB, tonB, rho, and deaD was confirmed by quantitative PCR, and the up-regulation of lpxD, omp6, secG, fabH, HP1285, HP0222, and HP0836 was confirmed by reverse transcription (RT)-PCR. The down-regulation of flaA, sodB, and HP0874 was confirmed by quantitative PCR, and the down-regulation of omp11 was confirmed by RT-PCR. The alteration of gene expression in H. pylori after adhesion to gastric cells in vitro suggests that changes in motility, outer membrane composition, and stress responses, among other changes, may be involved in gastric colonization.


Blood ◽  
2019 ◽  
Vol 134 (Supplement_1) ◽  
pp. 2504-2504
Author(s):  
Jessica Gasparello ◽  
Chiara Papi ◽  
Giulia Breveglieri ◽  
Elisabetta D'Aversa ◽  
Valentino Bezzerri ◽  
...  

In the Shwachman-Diamond syndrome (SDS), mutations of the gene encoding for the SBDS protein causes several hematological disorders, including neutropenia and myelodysplastic syndrome (MDS), with high risk of acute myeloid leukemia (AML).MicroRNAs (miRNAs) are small noncoding RNAs regulating gene expression by sequence-selective targeting of mRNAs, leading to translational repression or mRNA degradation. Low miRNA expression is associated with the accumulation of target mRNAs; high miRNA content causes low expression of target mRNAs. In almost all hematological disorders microRNAs were found dysregulated, and often these alterations of miRNAlevels are associated with the phenotype of the disease and tumor onset and progression. In order to verify possible involvement of microRNA in the SDS phenotype, we determined whether the microRNA pattern differentiate Lymphoblastoid Cell Cultures (LCC) derived from SDS patients from healthy subjects-derived LCC. To this aim Next Generation Sequencing (NGS) was performed using Illumina NextSeq500 platform and a signature of 11 up-regulated (hsa-miR-1260b, hsa-miR-1270, hsa-miR-1278, hsa-miR-1294, hsa-miR-296-5p, hsa-miR-34a-3p, hsa-miR-423-3p, hsa-miR-4513, hsa-miR-4521, hsa-miR-6732-3p, hsa-miR-744-3p) and 7 down-regulated (hsa-miR-148a-3p, hsa-miR-148a-5p, hsa-miR-181a-3p, hsa-miR-29b-3p, hsa-miR-29c-3p, hsa-miR-30d-5p, hsa-miR-660-5p) miRNAs was found in SDS cell cultures compared with controls. The differential expression of the microRNAs identified as dysregulated was confirmed by droplet-digital RT-PCR (ddRT-PCR). In consideration of the possible involvement of microRNAs in the STAT3 hyperactivation and interleukin-6 (IL-6) dysregulation, the 7 miRNAs down-regulated in SDS-LCC were analyzed. Among this miRNA set, miR-148a-5p might be of interest, because it targets the 3'UTR of IL-6 mRNA (position 71-78 of IL-6 3'UTR). MicroRNA miR-148a-5p down-regulation can participate to the IL-6 upregulation in SDS-LCC, demonstrated in LCC supernatants by Bio-Plex analysis of the secretome. Moreover, in consideration of the fact that LCC from SDS patients are characterized by up-regulated mTOR phosphorylation (Bezzerri et al, Sci Rep 2016) possibly associated with down-regulation of PTEN (a validated inhibitor of mTOR phosphorylation), PTEN transcript and protein levels were analyzed in SDS-LCC by RT-PCR and Western Blotting analysis. The data obtained suggest a down regulation of PTEN in SDS-LCC. In order to investigate the possible correlation between PTEN down-regulation and microRNA content in lymphoblastoid cells of SDS patients, we verified whether some of the up-regulated microRNAs found in the NGS analysis were potential regulators of PTEN. When the 11 up-regulated miRNAs were compared with 81 validated PTEN regulating miRNAs (www. mirtarbase.mbc.nctu.edu.tw), two microRNAs were identified: miR-34a-3p and miR-744-3p. Of relevance, the relative expression of miR-34a-3p and miR-744-3p was found variable among the cells from the different SDS patients. When the PTEN expression was related with the miR-34a-3p and miR-744-3p levels, an inverse correlation was found between the miR-34a-3p and miR-744-3p levels and PTEN gene expression. This study allows proposing molecules mimicking miR-148a-5p function in order to reduction of IL-6 expression. On the other hand, miR-34a-3p and miR-744-3p might be considered as possible targets of antagomiRNA molecules, for increasing PTEN expression in SDS patients. Altogether, these data support the concept themicroRNAs might participate to the phenotype of lymphoblastoid cells of SDS patients, therefore being potential molecular targets for miRNA therapeutics of Shwachman-Diamond syndrome. Acknowledgements: This study was supported by a FIR and a FAR fund of Ferrara University to AF, and by a fund from the Italian Ministry of Health (MOH) to VB, MB and GB. Disclosures Bezzerri: Marco Cipolli, Valentino Bezzerri, Baroukh Maurice Assael: Patents & Royalties: WO2018/050706 A1 "Method of treatment of Shwachman-Diamond syndrome". Cipolli:Marco Cipolli, Valentino Bezzerri, Baroukh Maurice Assael: Patents & Royalties: WO2018/050706 A1 "Method of treatment of Shwachman-Diamond syndrome".


Blood ◽  
2012 ◽  
Vol 120 (21) ◽  
pp. 1829-1829
Author(s):  
Haiming Chen ◽  
Jennifer Li ◽  
Kevin Delijani ◽  
Danielle Rauch ◽  
Kevin DeCorso ◽  
...  

Abstract Abstract 1829 Background: Enhanced angiogenesis in multiple myeloma (MM) is an important step in its tumor growth, invasion, and metastasis into the bone marrow. The bone marrow is a complex and dynamic microenvironment with multiple cell types contributing to niches that support myeloma tumor cell proliferation. One of the important microenvironmental factors, hypoxia-inducible factor 1α (HIF-1α), has been known to be associated with increased angiogenesis and metastatic potential as well as poor prognosis in MM. However, the role of HIF-1α in the etiology, pathogenesis and possible treatment of MM remains unclear. LIM domain-containing protein (LIMD1), a tumor suppressor molecular links prolyl hydroxylases (PHD1, 2 or 3) to von Hippel–Lindau (VHL) as a molecular scaffold, PHDs-LIMD1-VHL. This results in down-regulation of HIF-1α. Experiment design: Following informed consent, ten bone marrow aspirates and five biopsies were obtained from MM patients and healthy subjects, respectively. Bone marrow mononuclear cells (BMMCs) were isolated by using density-gradient centrifugation with Histopaque-1077 (Sigma, St Louis). For gene expression studies, total RNA was isolated from BMMCs. RNA was reverse-transcribed into cDNA and amplified using the Thermo-Script RT-PCR System and PCR performed again using the GeneAmp PCR System 9700. Protein expression in BMMCs from MM and healthy subjects was determined using Western blot analysis and immunohistochemical (IHC) staining. Results: The results showed that LIMD1 gene expression in BMMCs as assessed using RT-PCR in MM patients was reduced compared to healthy subjects. In addition, PHD1 gene expression in BMMCs from MM patients was markedly reduced whereas PHD2 and PHD3 expression was similar to healthy subjects' BMMCs. The gene expression of VHL1, VHL2, and VHL3 in BMMCs was similar in MM patients compared to healthy subjects. Notably, LIMD1 gene expression in BMMCs from patients with monoclonal gammopathy of undetermined significance and primary amyloidosis patients was lover than among patients with progressive MM. Furthermore, the results of IHC staining showed LIMD1 protein expression in biopsy samples from MM patients with progressive disease was deceased and associated with high expression of HIF-1α. We also determined LIMD1 gene expression in MM patients treated with or without bortezomib. The results showed that this proteasome inhibitor did not affect LIMD1 expression. Conclusion and discussion: LIMD1 expression is reduced with down-regulation of PHD1 and up-regulation of HIF-1α in MM patients. The proteasome inhibitor did not inhibit LIMD1 gene expression in our experiments although it has reported that bortezomib inhibits HIF-1α levels in MM. The results from these studies suggest that LIMD1 may be an important key regulator of HIF1-1a and angiogenesis in MM. It has been reported that knocking out the LIMD1 gene will lead to over-expression of a single gene K-Ras and result in the development of lung adenocarcinoma. We are currently investigating the other pathways that are impacted by the reduction of LIMD1 expression, and how this may lead to the pathogenesis of MM. Disclosures: No relevant conflicts of interest to declare.


2012 ◽  
Vol 50 (7-8) ◽  
pp. 529-537
Author(s):  
Ha Van Huan ◽  
Yong Wang ◽  
Siliang Zhang

2004 ◽  
Vol 171 (4S) ◽  
pp. 436-436
Author(s):  
John A. Petros ◽  
Audry N. Schuetz ◽  
Andrew N. Young ◽  
Q. Yin Goen ◽  
So Dug Lim ◽  
...  

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