Positional relationships between photoperiod response QTL and photoreceptor and vernalization genes in barley

2006 ◽  
Vol 112 (7) ◽  
pp. 1277-1285 ◽  
Author(s):  
P. Szűcs ◽  
I. Karsai ◽  
J. von Zitzewitz ◽  
K. Mészáros ◽  
L. L. D. Cooper ◽  
...  
2009 ◽  
Vol 35 (10) ◽  
pp. 1764-1770 ◽  
Author(s):  
Zhi-Ai GUO ◽  
Guang-Yao ZHAO ◽  
Zheng-Long REN ◽  
Ji-Zeng JIA

HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 481d-481
Author(s):  
Z. Wang ◽  
M.C. Acock ◽  
B. Acock

To develop models for estimating growth, flowering time and gum yield of opium poppy, we compared variability among five cultivars (T, L, B1, B2, B3) from different latitudes in three Southeast Asian countries. Variability in the relationships between gum yield, capsule volume, and dry weight was also examined. Plants were grown in six growth chambers at a 11-, 12-, 13-, 14-, 15-, or 16-h photoperiod (PP) with a 12-h 25/20 °C thermoperiod. The main capsule was lanced for opium gum at 10, 13, and 16 d after flowering (DAF). Plants were harvested at 21 DAF and separated into leaves, stems, and capsules. Flowering time for B2 was affected least by PP and B1 the most. Flowering times for B3, L, and T were similar across the range of PPs. All cultivars showed a significant increase in flowering time from 14 to 13 h PP. Cultivars that flowered late (such as B1) had greater biomass than those that flowered earlier. However, cultivars that flowered earlier (such as L) had more dry matter partitioned into capsule than late-flowering ones. B2, B3, and L had the highest gum yields while B1 had the lowest. Positive correlations were found between gum dry weight and capsule volume (or dry weight) for T and L, but no correlations were observed between these variables for B1, B2, and B3. Our results indicated that plant dry weight varied as much as 77% and flowering time varied up to 40% even though the critical photoperiod was the same for all cultivars. The ratio of gum yield to capsule dry weight were significantly different between B1 and T.


Euphytica ◽  
2019 ◽  
Vol 215 (9) ◽  
Author(s):  
Jinsheng Yu ◽  
Yunzheng Miao ◽  
Siqing Yang ◽  
Zhaobin Shi ◽  
Nana Miao ◽  
...  

2012 ◽  
Vol 38 (No. 3-4) ◽  
pp. 97-103 ◽  
Author(s):  
J. Košner ◽  
K. Pánková

For 17 cultivars of winter wheat (Triticum aestivum L.) different vernalization and photoperiod responses were detected. The effect of photoperiod sensitivity was not significantly changed by vernalization; different vernalization responses were probably due to the presence of multiple alleles at Vrn loci. The delay in heading depended on the vernalization deficit exponentially: y = Parameter (1) + (y0 – Parameter (1)) × EXP (Parameter (2) × (x – x0)). The dependence was shown to be general and significant for the given model in all the studied cultivars. Individual regressions characterised responses of cultivars to a deficit of vernalization treatment. Cluster analysis according to the characterisation obtained (full vernalization requirement, minimum vernalization requirement, insufficient vernalization and parameters of the dependence) showed the relationships between cultivars and enabled their grouping by similar profiles of vernalization, and, possibly, of photoperiod response. In individual cultivars, an attempt was made to use the model to predict performance for some agronomic traits.


2013 ◽  
Vol 64 (2) ◽  
pp. 100 ◽  
Author(s):  
Karen Cane ◽  
H. A. Eagles ◽  
D. A. Laurie ◽  
Ben Trevaskis ◽  
Neil Vallance ◽  
...  

Photoperiod and vernalisation genes are important for the adaptation of wheat to variable environments. Previously, using diagnostic markers and a large, unbalanced dataset from southern Australia, we estimated the effects on days to heading of frequent alleles of Vrn-A1, Vrn-B1, and Vrn-D1, and also two allelic classes of Ppd-D1. These genes accounted for ~45% of the genotypic variance for that trait. We now extend these analyses to further alleles of Ppd-D1, and four alleles of Ppd-B1 associated with copy number. Variation in copy number of Ppd-B1 occurred in our population, with one to four linked copies present. Additionally, in rare instances, the Ppd-B1 gene was absent (a null allele). The one-copy allele, which we labelled Ppd-B1b, and the three-copy allele, which we labelled Ppd-B1a, occurred through a century of wheat breeding, and are still frequent. With several distinct progenitors, the one-copy allele might not be homogenous. The two-copy allele, which we labelled Ppd-B1d, was generally introduced from WW15 (syn. Anza), and the four-copy allele, which we labelled Ppd-B1c, came from Chinese Spring. In paired comparisons, Ppd-B1a and Ppd-B1c reduced days to heading, but Ppd-B1d increased days to heading. Ppd-D1a, with a promoter deletion, Ppd-D1d, with a deletion in Exon 7, and Ppd-D1b, the intact allele, were frequent in modern Australian germplasm. Differences between Ppd-D1a and Ppd-D1d for days to heading under our field conditions depended on alleles of the vernalisation genes, confirming our previous report of large epistatic interactions between these classes of genes. The Ppd-D1b allele conferred a photoperiod response that might be useful for developing cultivars with closer to optimal heading dates from variable sowing dates. Inclusion of Ppd-B1 genotypes, and more precise resolution of Ppd-D1, increased the proportion of the genotypic variance attributed to these vernalisation and photoperiod genes to ~53%.


1950 ◽  
Vol 41 (8) ◽  
pp. 199-203 ◽  
Author(s):  
HAROLD H. SMITH
Keyword(s):  

1977 ◽  
Vol 17 (86) ◽  
pp. 417 ◽  
Author(s):  
DF Cameron ◽  
L't Mannetje ◽  
Mannetje L 't

The flowering of accessions from 12 Stylosanthes species was studied in two controlled environment experiments and a glasshouse experiment. In controlled environments photoperiod exerted a strong control over flowering with short day, day neutral and long day responses being recognized. High temperatures generally delayed flowering, increased the node of first flower and reduced the number of inflorescences, but acted as a modifier only of the basic control exerted by photoperiod. With natural photoperiods in the glasshouse, flowering responses were generally consistent with the photoperiod responses observed in controlled environments. The climatic adaptation of Stylosanthes species is discussed in relation to the alternative reproductive strategies of the photoperiod response types.


Author(s):  
Leonard Gol ◽  
Einar B Haraldsson ◽  
Maria von Korff

Abstract Drought impairs growth and spike development, and is therefore a major cause of yield losses in the temperate cereals barley and wheat. Here, we show that the photoperiod response gene PHOTOPERIOD-H1 (Ppd-H1) interacts with drought stress signals to modulate spike development. We tested the effects of a continuous mild and a transient severe drought stress on developmental timing and spike development in spring barley cultivars with a natural mutation in ppd-H1 and derived introgression lines carrying the wild-type Ppd-H1 allele from wild barley. Mild drought reduced the spikelet number and delayed floral development in spring cultivars but not in the introgression lines with a wild-type Ppd-H1 allele. Similarly, drought-triggered reductions in plant height, and tiller and spike number were more pronounced in the parental lines compared with the introgression lines. Transient severe stress halted growth and floral development; upon rewatering, introgression lines, but not the spring cultivars, accelerated development so that control and stressed plants flowered almost simultaneously. These genetic differences in development were correlated with a differential down-regulation of the flowering promotors FLOWERING LOCUS T1 and the BARLEY MADS-box genes BM3 and BM8. Our findings therefore demonstrate that Ppd-H1 affects developmental plasticity in response to drought in barley.


2010 ◽  
Vol 61 (9) ◽  
pp. 721 ◽  
Author(s):  
H. A. Eagles ◽  
Karen Cane ◽  
Haydn Kuchel ◽  
G. J. Hollamby ◽  
Neil Vallance ◽  
...  

Photoperiod and vernalization genes are important for the optimal adaptation of wheat to different environments. Diagnostic markers are now available for Vrn-A1, Vrn-B1, Vrn-D1 and Ppd-D1, with all four genes variable in southern Australian wheat-breeding programs. To estimate the effects of these genes on days to heading we used data from 128 field experiments spanning 24 years. From an analysis of 1085 homozygous cultivars and breeding lines, allelic variation for these four genes accounted for ~45% of the genotypic variance for days to heading. In the presence of the photoperiod-insensitive allele of Ppd-D1, differences between the winter genotype and genotypes with a spring allele at one of the genes ranged from 3.5 days for Vrn-B1 to 4.9 days for Vrn-D1. Smaller differences occurred between genotypes with a spring allele at one of the Vrn genes and those with spring alleles at two of the three genes. The shortest time to heading occurred for genotypes with spring alleles at both Vrn-A1 and Vrn-D1. Differences between the photoperiod-sensitive and insensitive alleles of Ppd-D1 depended on the genotype of the vernalization genes, being greatest when three spring alleles were present (11.8 days) and least when the only spring allele was at Vrn-B1 (3.7 days). Because of these epistatic interactions, for the practical purposes of using these genes for cross prediction and marker-assisted selection we concluded that using combinations of alleles of genes simultaneously would be preferable to summing effects of individual genes. The spring alleles of the vernalization genes responded differently to the accumulation of vernalizing temperatures, with the common spring allele of Vrn-A1 showing the least response, and the spring allele of Vrn-D1 showing a response that was similar to, but less than, a winter genotype.


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