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PsANT, the adenine nucleotide translocase of Puccinia striiformis, promotes cell death and fungal growth
Adenine nucleotide translocase (ANT) is a constitutive mitochondrial component that is involved in ADP/ATP exchange and mitochondrion-mediated apoptosis in yeast and mammals. However, little is known about the function of ANT in pathogenic fungi. In this study, we identified an ANT gene of Puccinia...
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Published in: | Scientific reports 2015-06, Vol.5 (1), p.11241-11241, Article 11241 |
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Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Adenine nucleotide translocase (ANT) is a constitutive mitochondrial component that is involved in ADP/ATP exchange and mitochondrion-mediated apoptosis in yeast and mammals. However, little is known about the function of ANT in pathogenic fungi. In this study, we identified an ANT gene of
Puccinia striiformis
f. sp.
tritici
(
Pst
), designated
PsANT
. The
PsANT
protein contains three typical conserved mitochondrion-carrier-protein (mito-carr) domains and shares more than 70% identity with its orthologs from other fungi, suggesting that ANT is conserved in fungi. Immuno-cytochemical localization confirmed the mitochondrial localization of
PsANT
in normal
Pst
hyphal cells or collapsed cells. Over-expression of
PsANT
indicated that
PsANT
promotes cell death in tobacco, wheat and fission yeast cells. Further study showed that the three mito-carr domains are all needed to induce cell death. qRT-PCR analyses revealed an in-planta induced expression of
PsANT
during infection. Knockdown of
PsANT
using a host-induced gene silencing system (HIGS) attenuated the growth and development of virulent
Pst
at the early infection stage but not enough to alter its pathogenicity. These results provide new insight into the function of
PsANT
in fungal cell death and growth and might be useful in the search for and design of novel disease control strategies. |
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ISSN: | 2045-2322 2045-2322 |
DOI: | 10.1038/srep11241 |