Chris Brien

Dr. Chris Brien

orcid

Research Focus & Metrics

Academic Career Length

52Years (1975-Present)

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

Representative Publications

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17 November 2016 in Nature Communications
Verified
Journal Article
Open access
NANadia Al-Tamimi
Nadia Al-Tamimi
CBChris Brien
Chris Brien
HOHelena Oakey
Helena Oakey
Bettina BergerBettina Berger
Bettina Berger
SSStephanie Saade
Stephanie Saade
SNSonia Negrao
Sonia Negrao
High-throughput phenotyping produces multiple measurements over time, which require new methods of analyses that are flexible in their quantification of plant growth and transpiration, yet are computationally economic. Here we develop such analyses and apply this to a rice population genotyped with a 700k SNP high-density array. Two rice diversity panels, indica and aus, containing a total of 553 genotypes, are phenotyped in waterlogged conditions. Using cubic smoothing splines to estimate plant growth and transpiration, we identify four time intervals that characterize the early responses of rice to salinity. Relative growth rate, transpiration rate and transpiration use efficiency (TUE) are analysed using a new association model that takes into account the interaction between treatment (control and salt) and genetic marker. This model allows the identification of previously undetected loci affecting TUE on chromosome 11, providing insights into the early responses of rice to salinity, in particular into the effects of salinity on plant growth and transpiration.

25 June 2015 in Plant Physiology
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Journal Article
Open access
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MCMalachy T. Campbell
Malachy T. Campbell
AKAvi C. Knecht
Avi C. Knecht
Bettina BergerBettina Berger
Bettina Berger
CBChris Brien
Chris Brien
DWDong Wang
Dong Wang
HWHarkamal Walia
Harkamal Walia
The genetic basis of dynamic salinity stress responses is elucidated using image-based phenomics and functional association analysis.

2 May 2017 in Scientific Reports
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Journal Article
Open access
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JAJudith Atieno
Judith Atieno
YLYongle Li
Yongle Li
Peter LangridgePeter Langridge
Peter Langridge
KDKate Dowling
Kate Dowling
CBChris Brien
Chris Brien
TSTim Sutton
Tim Sutton
Soil salinity results in reduced productivity in chickpea. However, breeding for salinity tolerance is challenging because of limited knowledge of the key traits affecting performance under elevated salt and the difficulty of high-throughput phenotyping for large, diverse germplasm collections. This study utilised image-based phenotyping to study genetic variation in chickpea for salinity tolerance in 245 diverse accessions. On average salinity reduced plant growth rate (obtained from tracking leaf expansion through time) by 20%, plant height by 15% and shoot biomass by 28%. Additionally, salinity induced pod abortion and inhibited pod filling, which consequently reduced seed number and seed yield by 16% and 32%, respectively. Importantly, moderate to strong correlation was observed for different traits measured between glasshouse and two field sites indicating that the glasshouse assays are relevant to field performance. Using image-based phenotyping, we measured plant growth rate under salinity and subsequently elucidated the role of shoot ion independent stress (resulting from hydraulic resistance and osmotic stress) in chickpea. Broad genetic variation for salinity tolerance was observed in the diversity panel with seed number being the major determinant for salinity tolerance measured as yield. This study proposes seed number as a selection trait in breeding salt tolerant chickpea cultivars.

1 June 1996 in Clinical Biomechanics
Verified
Journal Article
Closed access
PTPh Trott
Ph Trott
MPMj Pearcy
Mj Pearcy
SRSa Ruston
Sa Ruston
IFI Fulton
I Fulton
CBChris Brien
Chris Brien

4 August 2016 in Plant, Cell & Environment
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Journal Article
Open access
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JFJannatul Ferdous
Jannatul Ferdous
JSJuan Carlos Sanchez‐Ferrero
Juan Carlos Sanchez‐Ferrero
Peter LangridgePeter Langridge
Peter Langridge
LMLinda Milne
Linda Milne
JCJamil Chowdhury
Jamil Chowdhury
PTPenny Tricker
Penny Tricker
Drought is a crucial environmental constraint limiting crop production in many parts of the world. microRNA (miRNA) based gene regulation has been shown to act in several pathways, including crop response to drought stress. Sequence based profiling and computational analysis have revealed hundreds of miRNAs and their potential targets in different plant species under various stress conditions, but few have been biologically verified. In this study, 11 candidate miRNAs were tested for their expression profiles in barley. Differences in accumulation of only four miRNAs (Ath‐miR169b, Osa‐miR1432, Hv‐miRx5 and Hv‐miR166b/c) were observed between drought‐treated and well‐watered barley in four genotypes. miRNA targets were predicted using degradome analysis of two, different genotypes, and genotype‐specific target cleavage was observed. Inverse correlation of mature miRNA accumulation with miRNA target transcripts was also genotype dependent under drought treatment. Drought‐responsive miRNAs accumulated predominantly in mesophyll tissues. Our results demonstrate genotype‐specific miRNA regulation under drought stress and evidence for their role in mediating expression of target genes for abiotic stress response in barley.

11 April 2019 in BMC Plant Biology
Verified
Journal Article
Open access
PDF file
APAnh Pham
Anh Pham
AMAndreas Maurer
Andreas Maurer
KPKlaus Pillen
Klaus Pillen
CBChris Brien
Chris Brien
KDKate Dowling
Kate Dowling
TMTimothy J. March
Timothy J. March
Barley (Hordeum vulgare L.) is the fourth most important cereal crop worldwide. Barley production is compromised by many abiotic stresses including drought. Wild barley is a valuable source of alleles that can improve adaptation of cultivated barley to drought stress. In the present study, a nested association mapping population named HEB-25, consisting of 1420 BC1S3 lines that were developed by crossing 25 different wild barley accessions to the elite barley cultivar ‘Barke’, was evaluated under both control and drought-stressed conditions in the Australian Plant Phenomics Facility, University of Adelaide. Overall, 14 traits reflecting the performance of individual plants in each treatment were calculated from non-destructive imaging over time and destructive end-of-experiment measurements. For each trait, best linear unbiased estimators (BLUEs) were calculated and used for genome-wide association study (GWAS) analysis. Among the quantitative trait loci (QTL) identified for the 14 traits, many co-localise with known inflorescence and developmental genes. We identified a QTL on chromosome 4H where, under drought and control conditions, wild barley alleles increased biomass by 10 and 17% respectively compared to the Barke allele. Across all traits, QTL which increased phenotypic values were identified, providing a wider range of genetic diversity for the improvement of drought tolerance in barley.