Chemotaxis and oospore formation in Phytophthora sojae are controlled by G‐protein‐coupled receptors with a phosphatidylinositol phosphate kinase domain. Issue 2 (13th March 2013)
- Record Type:
- Journal Article
- Title:
- Chemotaxis and oospore formation in Phytophthora sojae are controlled by G‐protein‐coupled receptors with a phosphatidylinositol phosphate kinase domain. Issue 2 (13th March 2013)
- Main Title:
- Chemotaxis and oospore formation in Phytophthora sojae are controlled by G‐protein‐coupled receptors with a phosphatidylinositol phosphate kinase domain
- Authors:
- Yang, X.
Zhao, W.
Hua, C.
Zheng, X.
Jing, M.
Li, D.
Govers, F.
Meijer, H. J. G.
Wang, Y. - Abstract:
- <abstract abstract-type="main"> <title>Summary</title> <p>G‐protein‐coupled receptors (GPCRs) are key cellular components that mediate extracellular signals into intracellular responses. Genome mining revealed that <italic>Phytophthora</italic> spp. have over 60 GPCR genes among which a prominent class of 12 encoding novel proteins with an N‐terminal GPCR domain fused to a C‐terminal phosphatidylinositol phosphate kinase (PIPK) domain. This study focuses on two GPCR‐PIPKs (GKs) in <italic>Phytophthora sojae</italic>. <italic>PsGK4</italic> and <italic>PsGK5</italic> are differentially expressed during the life cycle with the highest expression in cysts and during cyst germination, and at late infection stages. In <italic>P. sojae</italic> transformants that constitutively express RFP‐tagged <italic>PsGK4</italic> and <italic>PsGK5</italic>, the fusion proteins in hyphae reside in small, rapidly moving vesicular‐like structures. Functional analysis using gene silencing showed that <italic>PsGK4</italic><italic>‐</italic>silenced transformants displayed higher levels of encystment and a reduced cyst germination rate when compared with the recipient strain. Moreover, GK4 deficiency (or reduction) resulted in severe defects in zoospore chemotaxis towards isoflavones and soybean roots. In contrast, <italic>PsGK5</italic><italic>‐</italic>silenced transformants exhibited no obvious defects in asexual development but oospore production was severely impaired. Both,<abstract abstract-type="main"> <title>Summary</title> <p>G‐protein‐coupled receptors (GPCRs) are key cellular components that mediate extracellular signals into intracellular responses. Genome mining revealed that <italic>Phytophthora</italic> spp. have over 60 GPCR genes among which a prominent class of 12 encoding novel proteins with an N‐terminal GPCR domain fused to a C‐terminal phosphatidylinositol phosphate kinase (PIPK) domain. This study focuses on two GPCR‐PIPKs (GKs) in <italic>Phytophthora sojae</italic>. <italic>PsGK4</italic> and <italic>PsGK5</italic> are differentially expressed during the life cycle with the highest expression in cysts and during cyst germination, and at late infection stages. In <italic>P. sojae</italic> transformants that constitutively express RFP‐tagged <italic>PsGK4</italic> and <italic>PsGK5</italic>, the fusion proteins in hyphae reside in small, rapidly moving vesicular‐like structures. Functional analysis using gene silencing showed that <italic>PsGK4</italic><italic>‐</italic>silenced transformants displayed higher levels of encystment and a reduced cyst germination rate when compared with the recipient strain. Moreover, GK4 deficiency (or reduction) resulted in severe defects in zoospore chemotaxis towards isoflavones and soybean roots. In contrast, <italic>PsGK5</italic><italic>‐</italic>silenced transformants exhibited no obvious defects in asexual development but oospore production was severely impaired. Both, <italic>PsGK4</italic>‐ and <italic>PsGK5</italic>‐silenced transformants showed reduced pathogenicity. These results point to involvement of GKs in zoospore behaviour, chemotaxis and oospore development, and suggest that PsGK4 and PsGK5 each head independent signalling pathways.</p> </abstract> … (more)
- Is Part Of:
- Molecular microbiology. Volume 88:Issue 2(2013)
- Journal:
- Molecular microbiology
- Issue:
- Volume 88:Issue 2(2013)
- Issue Display:
- Volume 88, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 88
- Issue:
- 2
- Issue Sort Value:
- 2013-0088-0002-0000
- Page Start:
- 382
- Page End:
- 394
- Publication Date:
- 2013-03-13
- Subjects:
- Molecular microbiology -- Periodicals
572.829 - Journal URLs:
- http://www.blackwell-synergy.com/servlet/useragent?func=showIssues&code=mmi&close=2003#C2003 ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2958 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/mmi.12191 ↗
- Languages:
- English
- ISSNs:
- 0950-382X
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5900.817960
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 3338.xml