Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Microbiology 155 (2009), 3748-3757; DOI  10.1099/mic.0.033217-0
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Supplementary Figure
Right arrow All Versions of this Article:
mic.0.033217-0v1
155/11/3748    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by Kumar, D.
Right arrow Articles by Saha, S.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kumar, D.
Right arrow Articles by Saha, S.
Agricola
Right arrow Articles by Kumar, D.
Right arrow Articles by Saha, S.
Microbiology 155 (2009), 3748-3757; DOI  10.1099/mic.0.033217-0
© 2009 Society for General Microbiology

The distribution pattern of proliferating cell nuclear antigen in the nuclei of Leishmania donovani

Devanand Kumar1, Neha Minocha1, Kalpana Rajanala2 and Swati Saha1

1 Department of Microbiology, University of Delhi South Campus, Benito Juarez Road, New Delhi 110021, India
2 National Institute of Immunology, Aruna Asaf Ali Marg, New Delhi 110067, India

DNA replication in eukaryotes is a highly conserved process marked by the licensing of multiple origins, with pre-replication complex assembly in G1 phase, followed by the onset of replication at these origins in S phase. The two strands replicate by different mechanisms, and DNA synthesis is brought about by the activity of the replicative DNA polymerases Pol {delta} and Pol {epsilon}. Proliferating cell nuclear antigen (PCNA) augments the processivity of these polymerases by serving as a DNA sliding clamp protein. This study reports the cloning of PCNA from the protozoan Leishmania donovani, which is the causative agent of the systemic disease visceral leishmaniasis. PCNA was demonstrated to be robustly expressed in actively proliferating L. donovani promastigotes. We found that the protein was present primarily in the nucleus throughout the cell cycle, and it was found in both proliferating procyclic and metacyclic promastigotes. However, levels of expression of PCNA varied through cell cycle progression, with maximum expression evident in G1 and S phases. The subnuclear pattern of expression of PCNA differed in different stages of the cell cycle; it formed distinct subnuclear foci in S phase, while it was distributed in a more diffuse pattern in G2/M phase and post-mitotic phase cells. These subnuclear foci are the sites of active DNA replication, suggesting that replication factories exist in Leishmania, as they do in higher eukaryotes, thus opening avenues for investigating other Leishmania proteins that are involved in DNA replication as part of these replication factories.

Correspondence
Swati Saha
ss5gp{at}yahoo.co.in


Abbreviations: DAPI, 4',6-diamidino-2-phenylindole; ORC, origin recognition complex; PCNA, proliferating cell nuclear antigen; pre-RC, pre-replication complex

The GenBank/EMBL/DDBJ accession number for the LdPCNA sequence reported in this paper is GQ249893.

A CLUSTALW analysis of LdPCNA and PCNAs from various trypanosomatids is available with the online version of this paper.







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 Society for General Microbiology.