Cargando…
The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing
Plasmodium falciparum origin recognition complex 1 (ORC1) protein has been implicated in DNA replication and silencing var gene family. However, the mechanism and the domain structure of ORC1 related to the regulation of var gene family are unknown. Here we show that the unique N-terminus of PfORC1...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384324/ https://www.ncbi.nlm.nih.gov/pubmed/22379140 http://dx.doi.org/10.1093/nar/gks202 |
_version_ | 1782236694784770048 |
---|---|
author | Deshmukh, Abhijit S. Srivastava, Sandeep Herrmann, Susann Gupta, Ashish Mitra, Pallabi Gilberger, Tim Wolf Dhar, Suman Kumar |
author_facet | Deshmukh, Abhijit S. Srivastava, Sandeep Herrmann, Susann Gupta, Ashish Mitra, Pallabi Gilberger, Tim Wolf Dhar, Suman Kumar |
author_sort | Deshmukh, Abhijit S. |
collection | PubMed |
description | Plasmodium falciparum origin recognition complex 1 (ORC1) protein has been implicated in DNA replication and silencing var gene family. However, the mechanism and the domain structure of ORC1 related to the regulation of var gene family are unknown. Here we show that the unique N-terminus of PfORC1 (PfORC1N(1–238)) is targeted to the nuclear periphery in vivo and this region binds to the telomeric DNA in vitro due to the presence of a leucine heptad repeats. Like PfORC1N(1–238), endogenous full length ORC1, was found to be associated with sub telomeric repeat regions and promoters of various var genes. Additionally, binding and propagation of ORC1 to telomeric and subtelomeric regions was severely compromised in PfSir2 deficient parasites suggesting the dependence of endogenous ORC1 on Sir2 for var gene regulation. This feature is not previously described for Plasmodium ORC1 and contrary to yeast Saccharomyces cerevisiae where ORC function as a landing pad for Sir proteins. Interestingly, the overexpression of ORC1N(1–238) compromises the binding of Sir2 at the subtelomeric loci and var gene promoters consistent with de-repression of some var genes. These results establish role of the N-terminus of PfORC1 in heterochromatin formation and regulation of var gene expression in co-ordination with Sir2 in P. falciparum. |
format | Online Article Text |
id | pubmed-3384324 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-33843242012-06-28 The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing Deshmukh, Abhijit S. Srivastava, Sandeep Herrmann, Susann Gupta, Ashish Mitra, Pallabi Gilberger, Tim Wolf Dhar, Suman Kumar Nucleic Acids Res Gene Regulation, Chromatin and Epigenetics Plasmodium falciparum origin recognition complex 1 (ORC1) protein has been implicated in DNA replication and silencing var gene family. However, the mechanism and the domain structure of ORC1 related to the regulation of var gene family are unknown. Here we show that the unique N-terminus of PfORC1 (PfORC1N(1–238)) is targeted to the nuclear periphery in vivo and this region binds to the telomeric DNA in vitro due to the presence of a leucine heptad repeats. Like PfORC1N(1–238), endogenous full length ORC1, was found to be associated with sub telomeric repeat regions and promoters of various var genes. Additionally, binding and propagation of ORC1 to telomeric and subtelomeric regions was severely compromised in PfSir2 deficient parasites suggesting the dependence of endogenous ORC1 on Sir2 for var gene regulation. This feature is not previously described for Plasmodium ORC1 and contrary to yeast Saccharomyces cerevisiae where ORC function as a landing pad for Sir proteins. Interestingly, the overexpression of ORC1N(1–238) compromises the binding of Sir2 at the subtelomeric loci and var gene promoters consistent with de-repression of some var genes. These results establish role of the N-terminus of PfORC1 in heterochromatin formation and regulation of var gene expression in co-ordination with Sir2 in P. falciparum. Oxford University Press 2012-07 2012-02-29 /pmc/articles/PMC3384324/ /pubmed/22379140 http://dx.doi.org/10.1093/nar/gks202 Text en © The Author(s) 2012. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene Regulation, Chromatin and Epigenetics Deshmukh, Abhijit S. Srivastava, Sandeep Herrmann, Susann Gupta, Ashish Mitra, Pallabi Gilberger, Tim Wolf Dhar, Suman Kumar The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title | The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title_full | The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title_fullStr | The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title_full_unstemmed | The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title_short | The role of N-terminus of Plasmodium falciparum ORC1 in telomeric localization and var gene silencing |
title_sort | role of n-terminus of plasmodium falciparum orc1 in telomeric localization and var gene silencing |
topic | Gene Regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3384324/ https://www.ncbi.nlm.nih.gov/pubmed/22379140 http://dx.doi.org/10.1093/nar/gks202 |
work_keys_str_mv | AT deshmukhabhijits theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT srivastavasandeep theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT herrmannsusann theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT guptaashish theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT mitrapallabi theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT gilbergertimwolf theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT dharsumankumar theroleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT deshmukhabhijits roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT srivastavasandeep roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT herrmannsusann roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT guptaashish roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT mitrapallabi roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT gilbergertimwolf roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing AT dharsumankumar roleofnterminusofplasmodiumfalciparumorc1intelomericlocalizationandvargenesilencing |