The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle

<p>Abstract</p> <p>Background</p> <p>Tc38 of <it>Trypanosoma cruzi </it>has been isolated as a single stranded DNA binding protein with high specificity for the poly [dT-dG] sequence. It is present only in Kinetoplastidae protozoa and its sequence lacks homo...

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Main Authors: Nardelli Sheila C, Maugeri Dante, Pérez-Díaz Leticia, Sotelo-Silveira José R, Pastro Lucía, Duhagon María A, Schenkman Sergio, Williams Noreen, Dallagiovanna Bruno, Garat Beatriz
Format: Article
Language:English
Published: BMC 2009-02-01
Series:BMC Microbiology
Online Access:http://www.biomedcentral.com/1471-2180/9/34
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spelling doaj-444f0165b1a247a4ab3e368ed56246e02020-11-25T00:26:47ZengBMCBMC Microbiology1471-21802009-02-01913410.1186/1471-2180-9-34The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycleNardelli Sheila CMaugeri DantePérez-Díaz LeticiaSotelo-Silveira José RPastro LucíaDuhagon María ASchenkman SergioWilliams NoreenDallagiovanna BrunoGarat Beatriz<p>Abstract</p> <p>Background</p> <p>Tc38 of <it>Trypanosoma cruzi </it>has been isolated as a single stranded DNA binding protein with high specificity for the poly [dT-dG] sequence. It is present only in Kinetoplastidae protozoa and its sequence lacks homology to known functional domains. Tc38 orthologues present in <it>Trypanosoma brucei </it>and <it>Leishmania </it>were proposed to participate in quite different cellular processes. To further understand the function of this protein in <it>Trypanosoma cruzi</it>, we examined its <it>in vitro </it>binding to biologically relevant [dT-dG] enriched sequences, its expression and subcellular localization during the cell cycle and through the parasite life stages.</p> <p>Results</p> <p>By using specific antibodies, we found that Tc38 protein from epimastigote extracts participates in complexes with the poly [dT-dG] probe as well as with the universal minicircle sequence (UMS), a related repeated sequence found in maxicircle DNA, and the telomeric repeat. However, we found that Tc38 predominantly localizes into the mitochondrion. Though Tc38 is constitutively expressed through non-replicating and replicating life stages of <it>T. cruzi</it>, its subcellular localization in the unique parasite mitochondrion changes according to the cell cycle stage. In epimastigotes, Tc38 is found only in association with kDNA in G1 phase. From the S to G2 phase the protein localizes in two defined and connected spots flanking the kDNA. These spots disappear in late G2 turning into a diffuse dotted signal which extends beyond the kinetoplast. This later pattern is more evident in mitosis and cytokinesis. Finally, late in cytokinesis Tc38 reacquires its association with the kinetoplast. In non-replicating parasite stages such as trypomastigotes, the protein is found only surrounding the entire kinetoplast structure.</p> <p>Conclusions</p> <p>The dynamics of Tc38 subcellular localization observed during the cell cycle and life stages support a major role for Tc38 related to kDNA replication and maintenance.</p> http://www.biomedcentral.com/1471-2180/9/34
collection DOAJ
language English
format Article
sources DOAJ
author Nardelli Sheila C
Maugeri Dante
Pérez-Díaz Leticia
Sotelo-Silveira José R
Pastro Lucía
Duhagon María A
Schenkman Sergio
Williams Noreen
Dallagiovanna Bruno
Garat Beatriz
spellingShingle Nardelli Sheila C
Maugeri Dante
Pérez-Díaz Leticia
Sotelo-Silveira José R
Pastro Lucía
Duhagon María A
Schenkman Sergio
Williams Noreen
Dallagiovanna Bruno
Garat Beatriz
The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
BMC Microbiology
author_facet Nardelli Sheila C
Maugeri Dante
Pérez-Díaz Leticia
Sotelo-Silveira José R
Pastro Lucía
Duhagon María A
Schenkman Sergio
Williams Noreen
Dallagiovanna Bruno
Garat Beatriz
author_sort Nardelli Sheila C
title The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
title_short The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
title_full The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
title_fullStr The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
title_full_unstemmed The <it>Trypanosoma cruzi </it>nucleic acid binding protein Tc38 presents changes in the intramitochondrial distribution during the cell cycle
title_sort <it>trypanosoma cruzi </it>nucleic acid binding protein tc38 presents changes in the intramitochondrial distribution during the cell cycle
publisher BMC
series BMC Microbiology
issn 1471-2180
publishDate 2009-02-01
description <p>Abstract</p> <p>Background</p> <p>Tc38 of <it>Trypanosoma cruzi </it>has been isolated as a single stranded DNA binding protein with high specificity for the poly [dT-dG] sequence. It is present only in Kinetoplastidae protozoa and its sequence lacks homology to known functional domains. Tc38 orthologues present in <it>Trypanosoma brucei </it>and <it>Leishmania </it>were proposed to participate in quite different cellular processes. To further understand the function of this protein in <it>Trypanosoma cruzi</it>, we examined its <it>in vitro </it>binding to biologically relevant [dT-dG] enriched sequences, its expression and subcellular localization during the cell cycle and through the parasite life stages.</p> <p>Results</p> <p>By using specific antibodies, we found that Tc38 protein from epimastigote extracts participates in complexes with the poly [dT-dG] probe as well as with the universal minicircle sequence (UMS), a related repeated sequence found in maxicircle DNA, and the telomeric repeat. However, we found that Tc38 predominantly localizes into the mitochondrion. Though Tc38 is constitutively expressed through non-replicating and replicating life stages of <it>T. cruzi</it>, its subcellular localization in the unique parasite mitochondrion changes according to the cell cycle stage. In epimastigotes, Tc38 is found only in association with kDNA in G1 phase. From the S to G2 phase the protein localizes in two defined and connected spots flanking the kDNA. These spots disappear in late G2 turning into a diffuse dotted signal which extends beyond the kinetoplast. This later pattern is more evident in mitosis and cytokinesis. Finally, late in cytokinesis Tc38 reacquires its association with the kinetoplast. In non-replicating parasite stages such as trypomastigotes, the protein is found only surrounding the entire kinetoplast structure.</p> <p>Conclusions</p> <p>The dynamics of Tc38 subcellular localization observed during the cell cycle and life stages support a major role for Tc38 related to kDNA replication and maintenance.</p>
url http://www.biomedcentral.com/1471-2180/9/34
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