Davinder Singh

Dr. Davinder Singh

Sydney Institute of Agriculture, Plant Breeding Institute Cobbitty, University of Sydney, Sydney, NSW 2567, Australia
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Research Focus & Metrics

Academic Career Length

26Years (2001-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 September 2010 in Theoretical and Applied Genetics
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Journal Article
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SHSybil A. Herrera-Foessel
Sybil A. Herrera-Foessel
ELEvans S. Lagudah
Evans S. Lagudah
JHJulio Huerta-Espino
Julio Huerta-Espino
MHMatt Hayden
Matt Hayden
HBHarbans S. Bariana
Harbans S. Bariana
RSRavi Prakash Singh
Ravi Prakash Singh

8 December 2010 in Euphytica
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Journal Article
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RSRavi Prakash Singh
Ravi Prakash Singh
JHJ. Huerta-Espino
J. Huerta-Espino
SBSridhar Bhavani
Sridhar Bhavani
SHS. A. Herrera-Foessel
S. A. Herrera-Foessel
Davinder SinghDavinder Singh
Davinder Singh
JCJose Crossa
Jose Crossa

4 August 2015 in Annual Review of Phytopathology
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Journal Article
Closed access
RPRobert Park
Robert Park
PGPrashant G. Golegaonkar
Prashant G. Golegaonkar
LDLida Derevnina
Lida Derevnina
KSKaranjeet S. Sandhu
Karanjeet S. Sandhu
HKHaydar Karaoglu
Haydar Karaoglu
Davinder SinghDavinder Singh
Davinder Singh
Leaf rust of barley is caused by the macrocyclic, heteroecious rust pathogen Puccinia hordei, with aecia reported from selected species of the genera Ornithogalum, Leopoldia, and Dipcadi, and uredinia and telia occurring on Hordeum vulgare, H. vulgare ssp. spontaneum, Hordeum bulbosum, and Hordeum murinum, on which distinct parasitic specialization occurs. Although Puccinia hordei is sporadic in its occurrence, it is probably the most common and widely distributed rust disease of barley. Leaf rust has increased in importance in recent decades in temperate barley-growing regions, presumably because of more intensive agricultural practices. Although total crop loss does not occur, under epidemic conditions yield reductions of up to 62% have been reported in susceptible varieties. Leaf rust is primarily controlled by the use of resistant cultivars, and, to date, 21 seedling resistance genes and two adult plant resistance (APR) genes have been identified. Virulence has been detected for most seedling resistance genes but is unknown for the APR genes Rph20 and Rph23. Other potentially new sources of APR have been reported, and additivity has been described for some of these resistances. Approaches to achieving durable resistance to leaf rust in barley are discussed.

20 August 2010 in Theoretical and Applied Genetics
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Journal Article
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CHColin W. Hiebert
Colin W. Hiebert
TFTom G. Fetch
Tom G. Fetch
TZTaye Zegeye
Taye Zegeye
JTJulian B. Thomas
Julian B. Thomas
DSDaryl J. Somers
Daryl J. Somers
DKDoug R. Knott
Doug R. Knott

15 March 2011 in Theoretical and Applied Genetics
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Journal Article
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Lee HickeyLee Hickey
Lee Hickey
WLW. Lawson
W. Lawson
GPG. J. Platz
G. J. Platz
MDM. Dieters
M. Dieters
VAV. N. Arief
V. N. Arief
JFJ. Franckowiak
J. Franckowiak

10 March 2017 in Plant Biotechnology Journal
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Journal Article
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ARAmy Rinaldo
Amy Rinaldo
BGBrian Gilbert
Brian Gilbert
RBRainer Boni
Rainer Boni
SKSimon G. Krattinger
Simon G. Krattinger
Davinder SinghDavinder Singh
Davinder Singh
MAMichael Ayliffe
Michael Ayliffe
Summary: The hexaploid wheat (Triticum aestivum) adult plant resistance gene, Lr34/Yr18/Sr57/Pm38/Ltn1, provides broad‐spectrum resistance to wheat leaf rust (Lr34), stripe rust (Yr18), stem rust (Sr57) and powdery mildew (Pm38) pathogens, and has remained effective in wheat crops for many decades. The partial resistance provided by this gene is only apparent in adult plants and not effective in field‐grown seedlings. Lr34 also causes leaf tip necrosis (Ltn1) in mature adult plant leaves when grown under field conditions. This D genome‐encoded bread wheat gene was transferred to tetraploid durum wheat (T. turgidum) cultivar Stewart by transformation. Transgenic durum lines were produced with elevated gene expression levels when compared with the endogenous hexaploid gene. Unlike nontransgenic hexaploid and durum control lines, these transgenic plants showed robust seedling resistance to pathogens causing wheat leaf rust, stripe rust and powdery mildew disease. The effectiveness of seedling resistance against each pathogen correlated with the level of transgene expression. No evidence of accelerated leaf necrosis or up‐regulation of senescence gene markers was apparent in these seedlings, suggesting senescence is not required for Lr34 resistance, although leaf tip necrosis occurred in mature plant flag leaves. Several abiotic stress‐response genes were up‐regulated in these seedlings in the absence of rust infection as previously observed in adult plant flag leaves of hexaploid wheat. Increasing day length significantly increased Lr34 seedling resistance. These data demonstrate that expression of a highly durable, broad‐spectrum adult plant resistance gene can be modified to provide seedling resistance in durum wheat.