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Most of its transcription is constitutive and driven by <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> polymerase <jats:styled-content style=\"fixed-case\">II<\/jats:styled-content>. <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> polymerase <jats:styled-content style=\"fixed-case\">I<\/jats:styled-content> (<jats:styled-content style=\"fixed-case\">Pol I<\/jats:styled-content>) transcribes not only ribosomal <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> genes, but also protein\u2010encoding genes, including variant surface glycoproteins (<jats:styled-content style=\"fixed-case\"><jats:italic>VSGs<\/jats:italic><\/jats:styled-content>) and procyclins. In <jats:styled-content style=\"fixed-case\"><jats:italic>T<\/jats:italic><\/jats:styled-content><jats:italic>. brucei<\/jats:italic>, histone <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 (<jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1) is required for <jats:styled-content style=\"fixed-case\"><jats:italic>VSG<\/jats:italic><\/jats:styled-content> silencing and chromatin condensation. However, whether <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 has a genome\u2010wide role in transcription is unknown. Here, using <jats:styled-content style=\"fixed-case\">RNA<\/jats:styled-content> sequencing we show that <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 depletion changes the expression of a specific cohort of genes. Interestingly, the predominant effect is partial loss of silencing of <jats:styled-content style=\"fixed-case\">Pol I<\/jats:styled-content> loci, such as <jats:styled-content style=\"fixed-case\"><jats:italic>VSG<\/jats:italic><\/jats:styled-content> and procyclin genes. Labelling of nascent transcripts with 4\u2010thiouridine showed that <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 depletion does not alter the level of labelled <jats:styled-content style=\"fixed-case\">Pol II<\/jats:styled-content> transcripts. In contrast, the levels of 4<jats:styled-content style=\"fixed-case\">sU<\/jats:styled-content>\u2010labelled <jats:styled-content style=\"fixed-case\">Pol I<\/jats:styled-content> transcripts were increased by two\u2010 to sixfold, suggesting that <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 preferentially blocks transcription at <jats:styled-content style=\"fixed-case\">Pol I<\/jats:styled-content> loci. Finally, we observed that parasites depleted of <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 grow almost normally in culture but they have a reduced fitness in mice, suggesting that <jats:styled-content style=\"fixed-case\">H<\/jats:styled-content>1 is important for host\u2013pathogen interactions.<\/jats:p>","DOI":"10.1111\/mmi.12677","type":"journal-article","created":{"date-parts":[[2014,6,19]],"date-time":"2014-06-19T15:20:32Z","timestamp":1403191232000},"page":"645-663","source":"Crossref","is-referenced-by-count":28,"title":["<scp><i>T<\/i><\/scp><i>rypanosoma brucei<\/i> histone <scp>H<\/scp>1 inhibits <scp>RNA<\/scp> polymerase <scp>I<\/scp> transcription and is important for parasite fitness <i>in vivo<\/i>"],"prefix":"10.1111","volume":"93","author":[{"given":"Ana C.","family":"Pena","sequence":"first","affiliation":[{"name":"Instituto de Medicina Molecular Faculdade de Medicina Universidade de Lisboa  Av. 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