Grecia Hernández-Hernández, Laura A Vera-Salazar, Guadalupe Gutiérrez-Escobedo, Nicolás Gómez-Hernández, Osney Leiva-Peláez, Alejandro De Las Peñas, Irene Castaño
{"title":"Abf1 负向调控 EPA1 的表达并影响白色念珠菌的粘附性。","authors":"Grecia Hernández-Hernández, Laura A Vera-Salazar, Guadalupe Gutiérrez-Escobedo, Nicolás Gómez-Hernández, Osney Leiva-Peláez, Alejandro De Las Peñas, Irene Castaño","doi":"10.1099/jmm.0.001905","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction</b>. Adherence is a major virulence trait in <i>Candida glabrata</i> that, in many strains, depends on the <i>EPA</i> (epithelial adhesin) genes, which confer the ability to adhere to epithelial and endothelial cells of the host. The <i>EPA</i> genes are generally found at subtelomeric regions, which makes them subject to subtelomeric silencing. In <i>C. glabrata</i>, subtelomeric silencing depends on different protein complexes, such as silent information regulator and yKu complexes, and other proteins, such as Repressor/activator protein 1 (Rap1) and Abf1. At the <i>EPA1</i> locus, which encodes the main adhesin Epa1, we previously found at least two <i>cis</i>-acting elements, the protosilencer Sil2126 and the negative element, that contribute to the propagation of silencing from the telomere to the subtelomeric region.<b>Hypothesis</b>. Abf1 binds to the regulatory regions of <i>EPA1</i> and other regions at the telomere E-R, thereby negatively regulating <i>EPA1</i> transcription.<b>Aim</b>. To determine whether Abf1 and Rap1 silencing proteins bind to previously identified <i>cis-</i>acting elements on the right telomere of chromosome E (E-R subtelomeric region), resulting in negative regulation of <i>EPA1</i> transcription and infer Abf1 and Rap1 recognition sites in <i>C. glabrata</i>.<b>Methodology</b>. We used chromatin immunoprecipitation (ChIP) followed by quantitative PCR to determine the binding sites for Abf1 and Rap1 in the intergenic regions between <i>EPA1</i> and <i>EPA2</i> and <i>HYR1</i> and <i>EPA1</i>, and mutants were used to determine the silencing level of the <i>EPA1</i> promoter region.<b>Results</b>. We found that Abf1 predominantly binds to the <i>EPA1</i> promoter region, leading to negative regulation of <i>EPA1</i> expression. Furthermore, the mutant <i>abf1-43</i>, which lacks the last 43 amino acids at its C-terminal end and is defective for subtelomeric silencing, exhibits hyperadherence to epithelial cells <i>in vitro</i> compared to the parental strain, suggesting that <i>EPA1</i> is derepressed. We also determined the motif-binding sequences for Abf1 and Rap1 in <i>C. glabrata</i> using data from the ChIP assays.<b>Conclusion</b>. Together these data indicate that Abf1 negatively regulates <i>EPA1</i> expression, leading to decreased adhesion of <i>C. glabrata</i> to epithelial cells.</p>","PeriodicalId":94093,"journal":{"name":"Journal of medical microbiology","volume":"73 10","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abf1 negatively regulates the expression of <i>EPA1</i> and affects adhesion in <i>Candida glabrata</i>.\",\"authors\":\"Grecia Hernández-Hernández, Laura A Vera-Salazar, Guadalupe Gutiérrez-Escobedo, Nicolás Gómez-Hernández, Osney Leiva-Peláez, Alejandro De Las Peñas, Irene Castaño\",\"doi\":\"10.1099/jmm.0.001905\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction</b>. Adherence is a major virulence trait in <i>Candida glabrata</i> that, in many strains, depends on the <i>EPA</i> (epithelial adhesin) genes, which confer the ability to adhere to epithelial and endothelial cells of the host. The <i>EPA</i> genes are generally found at subtelomeric regions, which makes them subject to subtelomeric silencing. In <i>C. glabrata</i>, subtelomeric silencing depends on different protein complexes, such as silent information regulator and yKu complexes, and other proteins, such as Repressor/activator protein 1 (Rap1) and Abf1. At the <i>EPA1</i> locus, which encodes the main adhesin Epa1, we previously found at least two <i>cis</i>-acting elements, the protosilencer Sil2126 and the negative element, that contribute to the propagation of silencing from the telomere to the subtelomeric region.<b>Hypothesis</b>. Abf1 binds to the regulatory regions of <i>EPA1</i> and other regions at the telomere E-R, thereby negatively regulating <i>EPA1</i> transcription.<b>Aim</b>. To determine whether Abf1 and Rap1 silencing proteins bind to previously identified <i>cis-</i>acting elements on the right telomere of chromosome E (E-R subtelomeric region), resulting in negative regulation of <i>EPA1</i> transcription and infer Abf1 and Rap1 recognition sites in <i>C. glabrata</i>.<b>Methodology</b>. We used chromatin immunoprecipitation (ChIP) followed by quantitative PCR to determine the binding sites for Abf1 and Rap1 in the intergenic regions between <i>EPA1</i> and <i>EPA2</i> and <i>HYR1</i> and <i>EPA1</i>, and mutants were used to determine the silencing level of the <i>EPA1</i> promoter region.<b>Results</b>. We found that Abf1 predominantly binds to the <i>EPA1</i> promoter region, leading to negative regulation of <i>EPA1</i> expression. Furthermore, the mutant <i>abf1-43</i>, which lacks the last 43 amino acids at its C-terminal end and is defective for subtelomeric silencing, exhibits hyperadherence to epithelial cells <i>in vitro</i> compared to the parental strain, suggesting that <i>EPA1</i> is derepressed. We also determined the motif-binding sequences for Abf1 and Rap1 in <i>C. glabrata</i> using data from the ChIP assays.<b>Conclusion</b>. Together these data indicate that Abf1 negatively regulates <i>EPA1</i> expression, leading to decreased adhesion of <i>C. glabrata</i> to epithelial cells.</p>\",\"PeriodicalId\":94093,\"journal\":{\"name\":\"Journal of medical microbiology\",\"volume\":\"73 10\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-10-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of medical microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1099/jmm.0.001905\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1099/jmm.0.001905","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Abf1 negatively regulates the expression of EPA1 and affects adhesion in Candida glabrata.
Introduction. Adherence is a major virulence trait in Candida glabrata that, in many strains, depends on the EPA (epithelial adhesin) genes, which confer the ability to adhere to epithelial and endothelial cells of the host. The EPA genes are generally found at subtelomeric regions, which makes them subject to subtelomeric silencing. In C. glabrata, subtelomeric silencing depends on different protein complexes, such as silent information regulator and yKu complexes, and other proteins, such as Repressor/activator protein 1 (Rap1) and Abf1. At the EPA1 locus, which encodes the main adhesin Epa1, we previously found at least two cis-acting elements, the protosilencer Sil2126 and the negative element, that contribute to the propagation of silencing from the telomere to the subtelomeric region.Hypothesis. Abf1 binds to the regulatory regions of EPA1 and other regions at the telomere E-R, thereby negatively regulating EPA1 transcription.Aim. To determine whether Abf1 and Rap1 silencing proteins bind to previously identified cis-acting elements on the right telomere of chromosome E (E-R subtelomeric region), resulting in negative regulation of EPA1 transcription and infer Abf1 and Rap1 recognition sites in C. glabrata.Methodology. We used chromatin immunoprecipitation (ChIP) followed by quantitative PCR to determine the binding sites for Abf1 and Rap1 in the intergenic regions between EPA1 and EPA2 and HYR1 and EPA1, and mutants were used to determine the silencing level of the EPA1 promoter region.Results. We found that Abf1 predominantly binds to the EPA1 promoter region, leading to negative regulation of EPA1 expression. Furthermore, the mutant abf1-43, which lacks the last 43 amino acids at its C-terminal end and is defective for subtelomeric silencing, exhibits hyperadherence to epithelial cells in vitro compared to the parental strain, suggesting that EPA1 is derepressed. We also determined the motif-binding sequences for Abf1 and Rap1 in C. glabrata using data from the ChIP assays.Conclusion. Together these data indicate that Abf1 negatively regulates EPA1 expression, leading to decreased adhesion of C. glabrata to epithelial cells.