全部 标题 作者
关键词 摘要

OALib Journal期刊
ISSN: 2333-9721
费用:99美元

查看量下载量

相关文章

更多...

Correlation of Vernalization Loci VRN-H1 and VRN-H2 and Growth Habit in Barley Germplasm

DOI: 10.1155/2013/924043

Full-Text   Cite this paper   Add to My Lib

Abstract:

Vernalization requirement is a key component in determining the overall fitness of developmental patterns of barley to its environment. We have used previously reported markers and spring-sown growth habit nursery to characterize the genotypes of barley germplasm in an applied barley breeding ground to establish a baseline of information required to understand the relationship between adaptation of autumn-sown barley germplasm in diverse regions with warm (W), moderate (M), or cold climates (C). This study revealed that twenty entries were detected with the presence of the vernalization critical region in VRN-H1 locus and complete presence of the three geneclusters ZCCT-Ha, -Hb, and -Hc in VRN-H2 locus represented as genotype vrn-H1/Vrn-H2 (V1w/V2w). Of these genotypes, 17 entries showed winter growth habit whereas the remaining three revealed facultative growth habit indicating reduced vernalization requirements possibly due to VRN-H3 and photoperiod sensitivity loci as compared to the landmark winter growth habit entries in this group. Twenty-four entries were detected with the lack of vernalization critical region in VRN-H1 locus but complete presence of the three geneclusters ZCCT-Ha, -Hb, and -Hc in VRN-H2 locus represented as genotype Vrn-H1/Vrn-H2 (V1s/V2w). However, only half of these germplasms were identified with spring growth habit in spring-sown nursery, and the rest of the germplasms in this group revealed facultative growth habits due to possible variation in the length of deletion in VRN-H1. Four germplasms showed vernalization insensitive phenotype due to the lack of a functional ZCCT-Ha and/or ZCCT-Hb alleles in VRN-H2 and the deletion in the vernalization critical region of VRN-H1. These germplasms revealed acomplete spring type growth habit. Only one entry showed reduced vernalization requirement solely due to the deletion in functional ZCCT-Hb allele in VRN-H2 and not due to the deletion in the vernalization critical region of VRN-H1. 1. Introduction Increases in yield and adaptation of cereals rest on life cycle adjustments to environmental constraints explained, in part, by the transition from vegetative to reproductive growth, flowering, and maturity [1, 2]. Optimal fitness of developmental patterns to the environment takes place when the crop utilizes most of inputs from the environment on the one hand and on the other hand escapes from deleterious effects of the adverse environmental conditions (i.e., frost stress and late maturity) [3], [4] leading to superior crop performance and yield potential [3]. Barley is a temperate

References

[1]  J. Cockram, E. Chiapparino, S. A. Taylor et al., “Haplotype analysis of vernalization loci in European barley germplasm reveals novel VRN-H1 alleles and a predominant winter VRN-H1/VRN-H2 multi-locus haplotype,” Theoretical and Applied Genetics, vol. 115, no. 7, pp. 993–1001, 2007.
[2]  J. Cockram, H. Jones, F. J. Leigh et al., “Control of flowering time in temperate cereals: genes, domestication, and sustainable productivity,” Journal of Experimental Botany, vol. 58, no. 6, pp. 1231–1244, 2007.
[3]  R. A. Richards, “Defining selection criteria to improve yield under drought,” Plant Growth Regulation, vol. 20, no. 2, pp. 157–166, 1996.
[4]  G. A. Slafer, “Genetic basis of yield as viewed from a crop physiologist’s perspective,” Annals of Applied Biology, vol. 142, no. 2, pp. 117–128, 2003.
[5]  D. L. Lister, S. Thaw, M. A. Bower et al., “Latitudinal variation in a photoperiod response gene in European barley: insight into the dynamics of agricultural spread from “historic” specimens,” Journal of Archaeological Science, vol. 36, no. 4, pp. 1092–1098, 2009.
[6]  J. R. Porter and M. Gawith, “Temperatures and the growth and development of wheat: a review,” European Journal of Agronomy, vol. 10, no. 1, pp. 23–36, 1999.
[7]  I. Karsai, K. Mészáros, L. Láng, P. M. Hayes, and Z. Bed?, “Multivariate analysis of traits determining adaptation in cultivated barley,” Plant Breeding, vol. 120, no. 3, pp. 217–222, 2001.
[8]  R. Takahashi and S. Yasuda, “Genetics of earliness and growth habit in barley,” in Barley Genetics II, R. A. Nilan, Ed., pp. 388–408, Washington State University Press, 1971.
[9]  S. Yasuda, J. Hayashi, and I. Moriya, “Genetic constitution for spring growth habit and some other characters in barley cultivars in the Mediterranean coastal regions,” Euphytica, vol. 70, no. 1-2, pp. 77–83, 1993.
[10]  J. Danyluk, N. A. Kane, G. Breton, A. E. Limin, D. B. Fowler, and F. Sarhan, “TaVRT-1, a putative transcription factor associated with vegetative to reproductive transition in cereals,” Plant Physiology, vol. 132, no. 4, pp. 1849–1860, 2003.
[11]  B. Trevaskis, D. J. Bagnall, M. H. Ellis, W. J. Peacock, and E. S. Dennis, “MADS box genes control vernalization-induced flowering in cereals,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 22, pp. 13099–13104, 2003.
[12]  B. Trevaskis, D. J. Bagnall, M. H. Ellis, J. Peacock, and E. J. Dennis, “MADS box genes control vernalization-induced fl owering in cereals,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 22, pp. 13099–13104, 2003.
[13]  L. Yan, A. Loukoianov, G. Tranquilli, M. Helguera, T. Fahima, and J. Dubcovsky, “Positional cloning of the wheat vernalization gene VRN1,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 10, pp. 6263–6268, 2003.
[14]  J. von Zitzewitz, P. Szucs, J. Dubcovsky et al., “Molecular and structural characterization of barley vernalization genes,” Plant Molecular Biology, vol. 59, no. 3, pp. 449–467, 2005.
[15]  D. Fu, P. Szucs, L. Yan et al., “Large deletions within the first intron in VRN-1 are associated with spring growth habit in barley and wheat,” Molecular Genetics and Genomics, vol. 273, no. 1, pp. 54–65, 2005.
[16]  J. Cockram, C. Norris, and D. M. O'Sullivan, “PCR-based markers diagnostic for spring and winter seasonal growth habit in barley,” Crop Science, vol. 49, no. 2, pp. 403–410, 2009.
[17]  L. Yan, A. Loukoianov, A. Blechl et al., “The wheat VRN2 gene is a flowering repressor down-regulated by vernalization,” Science, vol. 303, no. 5664, pp. 1640–1644, 2004.
[18]  J. Dubcovsky, C. Chen, and L. Yan, “Molecular characterization of the allelic variation at the VRN-H2 vernalization locus in barley,” Molecular Breeding, vol. 15, no. 4, pp. 395–407, 2005.
[19]  D. A. Laurie, N. Pratchett, J. H. Bezant, and J. W. Snape, “RFLP mapping of five major genes and eight quantitative trait loci controlling flowering time in a winter × spring barley (Hordeum vulgare L.) cross,” Genome, vol. 38, no. 3, pp. 575–585, 1995.
[20]  L. Yan, D. Fu, C. Li et al., “The wheat and barley vernalization gene VRN3 is an orthologue of FT,” Proceedings of the National Academy of Sciences of the United States of America, vol. 103, no. 51, pp. 19581–19586, 2006.
[21]  S. Faure, J. Higgins, A. Turner, and D. A. Laurie, “The FLOWERING LOCUS T-like gene family in barley (Hordeumvulgare),” Genetics, vol. 176, no. 1, pp. 599–609, 2007.
[22]  B. Trevaskis, M. N. Hemming, W. J. Peacock, and E. S. Dennis, “HvVRN2 responds to daylength, whereas HvVRN1 is regulated by vernalization and developmental status,” Plant Physiology, vol. 140, no. 4, pp. 1397–1405, 2006.
[23]  A. Turner, J. Beales, S. Faure, R. P. Dunford, and D. A. Laurie, “The pseudo-response regulator Ppd-H1 provides adaptation to photoperiod in barley,” Science, vol. 310, no. 5750, pp. 1031–1034, 2005.
[24]  M. N. Hemming, W. J. Peacock, E. S. Dennis, and B. Trevaskis, “Low-temperature and daylength cues are integrated to regulate Flowering Locus T in barley,” Plant Physiology, vol. 147, no. 1, pp. 355–366, 2008.
[25]  K. Koti, I. Karsai, P. Szucs et al., “Validation of the two-gene epistatic model for vernalization response in a Winter Spring barley cross,” Euphytica, vol. 152, no. 1, pp. 17–24, 2006.
[26]  P. Sz?cs, J. S. Skinner, I. Karsai et al., “Validation of the VRN-H2/VRN-H1 epistatic model in barley reveals that intron length variation in VRN-H1 may account for a continuum of vernalization sensitivity,” Molecular Genetics and Genomics, vol. 277, no. 3, pp. 249–261, 2007.
[27]  M. N. Hemming, S. Fieg, W. J. Peacock, E. S. Dennis, and B. Trevaskis, “Regions associated with repression of the barley (Hordeum vulgare) VERNALIZATION1 gene are not required for cold induction,” Molecular Genetics and Genomics, vol. 282, no. 2, pp. 107–117, 2009.
[28]  M. C. Casao, E. Igartua, I. Karsai, J. M. Lasa, M. P. Gracia, and A. M. Casas, “Expression analysis of vernalization and day-length response genes in barley (Hordeum vulgare L.) indicates that VRNH2 is a repressor of PPDH2 (HvFT3) under long days,” Journal of Experimental Botany, vol. 62, no. 6, pp. 1939–1949, 2011.

Full-Text

Contact Us

[email protected]

QQ:3279437679

WhatsApp +8615387084133