ENAapplication/xmlftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/069/SRR15862569/SRR15862569_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/075/SRR15862575/SRR15862575_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/067/SRR15862567/SRR15862567_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/077/SRR15862577/SRR15862577_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/071/SRR15862571/SRR15862571_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/077/SRR15862577/SRR15862577_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/074/SRR15862574/SRR15862574_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/073/SRR15862573/SRR15862573_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/069/SRR15862569/SRR15862569_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/075/SRR15862575/SRR15862575_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/068/SRR15862568/SRR15862568_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/072/SRR15862572/SRR15862572_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/066/SRR15862566/SRR15862566_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/076/SRR15862576/SRR15862576_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/068/SRR15862568/SRR15862568_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/074/SRR15862574/SRR15862574_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/072/SRR15862572/SRR15862572_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/071/SRR15862571/SRR15862571_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/070/SRR15862570/SRR15862570_1.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/076/SRR15862576/SRR15862576_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/073/SRR15862573/SRR15862573_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/070/SRR15862570/SRR15862570_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/067/SRR15862567/SRR15862567_2.fastq.gzftp://ftp.sra.ebi.ac.uk/vol1/fastq/SRR158/066/SRR15862566/SRR15862566_1.fastq.gzprimaryOK200GenomicsKurchatov Instituthttps://www.ebi.ac.uk/ena/browser/view/PRJNA761969investigating of a regulatory activity of antirestriction genes using RNA-seq method. The ardA genes from both conjugative plasmid (pKM101) and bacterial chromosome (B. bifidum) were cloned into E. coli K12 (strain AB1157) and total RNA were extracted from the clones. The results of RNA-seq were analyzed to estimate each E. coli gene activities and were compared to control strains without ardA. This analysis was performed for bacterial antirestrictases, but also for classical plasmid ardA genesENAribonucleic acid, Acid, RNA, Ribonucleic, Bacterium coli, Materials, Escherichia/Shigella coli, Genetic, determination, ribose nucleic acid, Non Polyadenylated RNA, ribonucleic acids, Non-Polyadenylated, Gene, RNS, Ribonucleic Acid, Cistrons, E. coli, Non-Polyadenylated RNA, Bacterium coli commune, Material, Bacillus coli, yeast nucleic acid, Ribonukleinsaeure, chemical analysis, Gene Products, pentosenucleic acids, Genetic Materials, Cistron, Ribonucleic acids, assay, Enterococcus coli, Genetic Material., Non Polyadenylated, RNA Gene ProductsfalseE. coli RNA seq analysis in the present of antirestriction genes ardA2023-05-172021-09-17PRJNA761969