Gustavo A. Niño-Vega, Françoise Sorais, Gioconda San-Blas
{"title":"巴西副球虫菌丝期CHS5和CHS4基因的转录水平响应外部渗透压、氧化应激和葡萄糖浓度的变化","authors":"Gustavo A. Niño-Vega, Françoise Sorais, Gioconda San-Blas","doi":"10.1016/j.mycres.2009.07.005","DOIUrl":null,"url":null,"abstract":"<div><p>The complete sequence of <em>Paracoccidioides brasiliensis CHS5</em> gene, encoding a putative chitin synthase revealed a 5583<!--> <!-->nt open reading frame, interrupted by three introns of 82, 87 and 97<!--> <!-->bp (GenBank Accession No <span>EF654132</span><svg><path></path></svg>). The deduced protein contains 1861 amino acids with a predicted molecular weight of 206.9<!--> <!-->kDa. Both its large size and the presence of a N-terminal region of approx. 800 residues with a characteristic putative myosin motor-like domain, allow us to include PbrChs5 into class V fungal chitin synthases. Sequence analysis of over 4<!--> <!-->kb from the 5′ UTR region in <em>CHS5</em>, revealed the presence of a previously reported <em>CHS4</em> gene in <em>P. brasiliensis</em>, arranged in a head-to-head configuration with <em>CHS5</em>. A motif search in this shared region showed the presence of stress response elements (STREs), three binding sites for the transcription activators Rlm1p (known to be stimulated by hypo-osmotic stress) and clusters of Adr1 (related to glucose repression). A quantitative RT-PCR analysis pointed to changes in transcription levels for both genes following oxidative stress, alteration of external osmolarity and under glucose-repressible conditions, suggesting a common regulatory mechanism of transcription.</p></div>","PeriodicalId":19045,"journal":{"name":"Mycological research","volume":"113 10","pages":"Pages 1091-1096"},"PeriodicalIF":0.0000,"publicationDate":"2009-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.mycres.2009.07.005","citationCount":"13","resultStr":"{\"title\":\"Transcription levels of CHS5 and CHS4 genes in Paracoccidioides brasiliensis mycelial phase, respond to alterations in external osmolarity, oxidative stress and glucose concentration\",\"authors\":\"Gustavo A. Niño-Vega, Françoise Sorais, Gioconda San-Blas\",\"doi\":\"10.1016/j.mycres.2009.07.005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The complete sequence of <em>Paracoccidioides brasiliensis CHS5</em> gene, encoding a putative chitin synthase revealed a 5583<!--> <!-->nt open reading frame, interrupted by three introns of 82, 87 and 97<!--> <!-->bp (GenBank Accession No <span>EF654132</span><svg><path></path></svg>). The deduced protein contains 1861 amino acids with a predicted molecular weight of 206.9<!--> <!-->kDa. Both its large size and the presence of a N-terminal region of approx. 800 residues with a characteristic putative myosin motor-like domain, allow us to include PbrChs5 into class V fungal chitin synthases. Sequence analysis of over 4<!--> <!-->kb from the 5′ UTR region in <em>CHS5</em>, revealed the presence of a previously reported <em>CHS4</em> gene in <em>P. brasiliensis</em>, arranged in a head-to-head configuration with <em>CHS5</em>. A motif search in this shared region showed the presence of stress response elements (STREs), three binding sites for the transcription activators Rlm1p (known to be stimulated by hypo-osmotic stress) and clusters of Adr1 (related to glucose repression). A quantitative RT-PCR analysis pointed to changes in transcription levels for both genes following oxidative stress, alteration of external osmolarity and under glucose-repressible conditions, suggesting a common regulatory mechanism of transcription.</p></div>\",\"PeriodicalId\":19045,\"journal\":{\"name\":\"Mycological research\",\"volume\":\"113 10\",\"pages\":\"Pages 1091-1096\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2009-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.mycres.2009.07.005\",\"citationCount\":\"13\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Mycological research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0953756209001208\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Mycological research","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0953756209001208","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Transcription levels of CHS5 and CHS4 genes in Paracoccidioides brasiliensis mycelial phase, respond to alterations in external osmolarity, oxidative stress and glucose concentration
The complete sequence of Paracoccidioides brasiliensis CHS5 gene, encoding a putative chitin synthase revealed a 5583 nt open reading frame, interrupted by three introns of 82, 87 and 97 bp (GenBank Accession No EF654132). The deduced protein contains 1861 amino acids with a predicted molecular weight of 206.9 kDa. Both its large size and the presence of a N-terminal region of approx. 800 residues with a characteristic putative myosin motor-like domain, allow us to include PbrChs5 into class V fungal chitin synthases. Sequence analysis of over 4 kb from the 5′ UTR region in CHS5, revealed the presence of a previously reported CHS4 gene in P. brasiliensis, arranged in a head-to-head configuration with CHS5. A motif search in this shared region showed the presence of stress response elements (STREs), three binding sites for the transcription activators Rlm1p (known to be stimulated by hypo-osmotic stress) and clusters of Adr1 (related to glucose repression). A quantitative RT-PCR analysis pointed to changes in transcription levels for both genes following oxidative stress, alteration of external osmolarity and under glucose-repressible conditions, suggesting a common regulatory mechanism of transcription.