{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,18]],"date-time":"2026-09-18T19:27:03Z","timestamp":1789759623884,"version":"4.0.1"},"reference-count":29,"publisher":"Microbiology Society","issue":"6","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2005,6,1]]},"abstract":"<jats:p>The Fe(III)-reducing micro-organism <jats:italic>Geobacter sulfurreducens<\/jats:italic> requires an outer-membrane <jats:italic>c<\/jats:italic>-type cytochrome, OmcB, for Fe(III) reduction, but a related cytochrome, OmcC, which is 73\u200a% identical to OmcB, is not required. The <jats:italic>omcB<\/jats:italic> and <jats:italic>omcC<\/jats:italic> genes are part of a tandem chromosomal duplication consisting of two repeated clusters of four genes. The 2\u00b77\u2005kb sequences preceding <jats:italic>omcB<\/jats:italic> and <jats:italic>omcC<\/jats:italic> are identical with the exception of a single base pair change. Studies that combined genetic, Northern blotting and primer extension analyses demonstrated that both <jats:italic>omcB<\/jats:italic> and <jats:italic>omcC<\/jats:italic> are transcribed as monocistronic and polycistronic (<jats:italic>orf1<\/jats:italic>-<jats:italic>orf2<\/jats:italic>-<jats:italic>omcB<\/jats:italic>\/<jats:italic>omcC<\/jats:italic>) transcripts. All of the promoters for the various transcripts were found to be located within the 2\u00b77\u2005kb identical region upstream of <jats:italic>omcB<\/jats:italic> and <jats:italic>omcC<\/jats:italic>. The sequences of the promoter regions for the two monocistronic transcripts are identical and equidistant from the <jats:italic>omcB<\/jats:italic> or <jats:italic>omcC<\/jats:italic> start codons. The promoters for the two polycistronic transcripts, in contrast, are distinct. One is specific for transcription of <jats:italic>orf1<\/jats:italic>-<jats:italic>orf2<\/jats:italic>-<jats:italic>omcB<\/jats:italic> and the other is associated with transcription of <jats:italic>orf1<\/jats:italic>-<jats:italic>orf2<\/jats:italic>-<jats:italic>omcC<\/jats:italic>. Studies with an RpoS-deficient mutant suggested that transcription from all four promoters is RpoS dependent under one or more growth conditions. Deletion of <jats:italic>orfR<\/jats:italic>, a gene immediately upstream of <jats:italic>orf1<\/jats:italic>-<jats:italic>orf2<\/jats:italic>-<jats:italic>omcB<\/jats:italic> that encodes a putative transcriptional regulator, significantly lowered the <jats:italic>omcB<\/jats:italic> transcription when Fe(III) was the electron acceptor and partially inhibited Fe(III) reduction. In contrast, levels of <jats:italic>omcC<\/jats:italic> transcripts were unaffected in the <jats:italic>orfR<\/jats:italic> mutant. These results indicate that <jats:italic>omcB<\/jats:italic> and <jats:italic>omcC<\/jats:italic> operons represent a rare instance in which duplicated operons, located in tandem on the chromosome, have different transcriptional regulation.<\/jats:p>","DOI":"10.1099\/mic.0.27870-0","type":"journal-article","created":{"date-parts":[[2005,6,7]],"date-time":"2005-06-07T19:33:51Z","timestamp":1118172831000},"page":"1761-1767","source":"Crossref","is-referenced-by-count":49,"title":["Regulation of two highly similar genes, omcB and omcC, in a 10\u2005kb chromosomal duplication in Geobacter sulfurreducens"],"prefix":"10.1099","volume":"151","author":[{"given":"Ching","family":"Leang","sequence":"first","affiliation":[{"name":"Department of Microbiology, 203 Morrill Science Center IVN, 639 North Pleasant St, University of Massachusetts at Amherst, Amherst, MA 01003, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Derek 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