In the December Nature Biotechnology Selinger et al. use an Escherichia coli oligonucleotide array with 30-base-pair resolution to detect antisense transcripts, new open reading frames (ORFs), and transcription starts and stops (Nat Biotechnol 2000, 18:1262-1268). The 295,936 elements of the array do not come without their problems. The sheer size and complexity of the array means that there is a huge amount of cross hybridization detected by missense probes. But the use of many probes within th
In the December Nature Biotechnology Selinger et al. use an Escherichia coli oligonucleotide array with 30-base-pair resolution to detect antisense transcripts, new open reading frames (ORFs), and transcription starts and stops (Nat Biotechnol 2000, 18:1262-1268). The 295,936 elements of the array do not come without their problems. The sheer size and complexity of the array means that there is a huge amount of cross hybridization detected by missense probes. But the use of many probes within the same gene allows Selinger et al. to identify many genes that are up- or down-regulated in stationary phase. They also confirm transcription stop and start sites for two genes. Scanning for antisense transcripts suggests that there is a low level of transcription throughout the genome, probably from replication-induced and readthrough transcription.
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