Summary
There is no comprehensive listing of genetic resources and potential donors for drought resistance. Sporadic data may sometime be found in seed banks but the quality of the data is uncertain. This chapter attempts to present the available groups of actual and potential genetic resources as derived from past and current literature. Five groups are recognized. These are listed by the order of their relative genetic compatibility with cultivated breeding germplasm.
While it is to be expected that breeders tend to search for donors of drought resistance among distant germplasm, it is quite apparent today that normal agronomic breeding germplasm may often carry latent genetic variation for drought resistance and this should be the first resource of choice. Landraces from dry habitats have been used successfully in breeding for water limited environments, whether towards developing open pollinated varieties or hybrids. Wild species and progenitors of our cultivated crops were always on the agenda as possible donors for drought resistance. Attempts at using these resources have increased in recent years and this chapter evaluates their potential and real contribution. Transgenic plants are first developed as a tool in functional genomics. They can constitute a realistic step towards transferring useful genes into a target crop plant, and as such they are an important genetic resource. Their importance is increasing as their drought phenotyping improves. Lastly, resurrection plants which survive extreme desiccation under harsh environments have always excited the imagination of biologists. Research on the nature of their tolerance may open new avenues for their use as donors of important genes for drought resistance.
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References
Baalbaki R, Hajj-Hassan N, Zurayk R (2006) Aegilops species from semiarid areas of Lebanon: variation in quantitative attributes under water stress. Crop Sci 46:799–806
Babu CR, Zhang J, Blum A et al (2004) HVA1, a LEA gene from barley confers dehydration tolerance in transgenic rice (Oryza sativa L) via cell membrane protection. Plant Sci 166:855–862
Bahieldin A, Mahfouz HT, Eissa HF et al (2005) Field evaluation of transgenic wheat plants stably expressing the HVA1 gene for drought tolerance. Physiol Plant 123:421–427
Bhattarai T, Fettig S (2005) Isolation and characterization of a dehydrin gene from Cicer pinnatifidum, a drought-resistant wild relative of chickpea. Physiol Plant 123:452–458
Blum A, Sullivan CY (1986) The comparative drought resistance of landraces of sorghum and millet from dry and humid regions. Ann Bot 57:835–846
Blum A, Gozlan G, Mayer J (1981) The manifestation of dehydration avoidance in wheat breeding germplasm. Crop Sci 21:495–499
Blum A, Ebercon A, Sinmena B et al (1983) Drought resistance reactions of wild emmer (T. dicoccoides) and wild emmer x wheat derivatives. In: Proceedings of the 6th international wheat genetics symposium, Kyoto, pp 433–438
Blum A, Golan G, Mayer J et al (1989) The drought response of landraces of wheat from the Northern Negev desert in Israel. Euphytica 43:87–96
Blum A, Munns R, Passioura JB et al (1996) Genetically engineered plants resistant to soil drying and salt stress: how to interpret osmotic relations? Plant Physiol 110:1051
Cairns JE, Botwright Acun TL, Simborio FA et al (2009) Identification of deletion mutants with improved performance under water-limited environments in rice (Oryza sativa L). Field Crops Res 114:159–168
Carver BF, Nevo E (1990) Genetic diversity of photosynthetic characters in native populations of Triticum-dicoccoides. Photosynth Res 25:119–128
Castiglioni P, Warner D, Bensen RJ et al (2008) Bacterial RNA chaperones confer abiotic stress tolerance in plants and improved grain yield in maize under water-limited conditions. Plant Physiol 147:446–455
Cattivelli L, Rizza F, Badeck FW et al (2008) Drought tolerance improvement in crop plants: an integrated view from breeding to genomics. Field Crops Res 105:1–14
Ceccarelli S, Grando S (1991) Environment of selection and type of germplasm in barley breeding for low-yielding conditions. Euphytica 57:207–219
Ceccarelli S, Grando S, Impiglia A (1998) Choice of selection strategy in breeding barley for stress environments. Euphytica 10:307–318
Dingkuhn M, Jones MP, Johnson DE et al (1998) Growth and yield potential of Oryza sativa and O. glaberrima upland rice cultivars and their interspecific progenies. Field Crops Res 57:57–69
Gallardo M, Jackson LE, Thompson RB (1996) Shoot and root physiological responses to localized zones of soil moisture in cultivated and wild lettuce (Lactuca spp). Plant Cell Environ 9:1169–1178
Gororo NN, Eagles HA, Eastwood RF et al (2002) Use of Triticum tauschii to improve yield of wheat in low-yielding environments. Euphytica 123:241–254
Hamdi A, Erskine W (1996) Reaction of wild species of the genus lens to drought. Euphytica 91:173–179
Huang J, Hirji R, Adam L et al (2000) Genetic engineering of glycinebetaine production toward enhancing stress tolerance in plants: metabolic limitations. Plant Physiol 122:747–756
Humphreys J, Harper JA, Armstead IP et al (2005) Introgression-mapping of genes for drought resistance transferred from Festuca arundinacea var glaucescens into Lolium multiflorum. Theor Appl Genet 110:579–587
Ito Y, Katsura K, Maruyama K et al (2006) Functional analysis of rice DREB1/CBF-type transcription factors involved in cold-responsive gene expression in transgenic rice. Plant Cell Physiol 47:141–153
James VA, Neibaur I, Altpeter F (2008) Stress inducible expression of the DREB1A transcription factor from xeric, Hordeum spontaneum L in turf and forage grass (Paspalum notatum Flugge) enhances abiotic stress tolerance. Transgenic Res 17:93–104
Jenks MA, Hasegawa PM, Mohan Jain S (eds) (2007) Advances in molecular breeding towards drought and salt tolerant crops. Springer, Dordrecht
Jiang Q, Zhang J-Y, Guo X et al (2010) Improvement of drought tolerance in white clover (Trifolium repens) by transgenic expression of a transcription factor gene WXP1. Funct Plant Biol 37:157–165
Johnson WC, Jackson LE, Ochoa O et al (2000) Lettuce, a shallow-rooted crop, and Lactuca serriola, its wild progenitor, differ at QTL determining root architecture and deep soil water exploitation. Theor Appl Genet 101:1066–1073
Lafitte HR, Li ZK, Vijayakumar CHM et al (2006) Improvement of rice drought tolerance through backcross breeding: evaluation of donors and selection in drought nurseries. Field Crops Res 96:77–86
Lakew B, Semeane Y, Alemayehu F et al (1997) Exploiting the diversity of barley landraces in Ethiopia. Genet Resour Crop Evol 44:109–116
Lal S, Gulyani V, Khurana P (2008) Overexpression of HVA1 gene from barley generates tolerance to salinity and water stress in transgenic mulberry (Morus indica). Trans Res 17:651–663
Liu L, Lafitte R, Guan D (2004) Wild Oryza species as potential sources of drought-adaptive traits. Euphytica 138:149–161
Lv S, Yang A, Zhang K et al (2007) Increase of glycinebetaine synthesis improves drought tolerance in cotton. Mol Breed 20:233–248
Marshall AH, Rascle C, Abberton MT et al (2001) Introgression as a route to improved drought tolerance in white clover (Trifolium repens L). J Agron Crop Sci 187:11–18
Moore JP, Le NT, Brandt WF et al (2009) Towards a systems-based understanding of plant desiccation tolerance. Trends Plant Sci 14:110–117
Nakashima K, Ito Y, Yamaguchi-Shinozaki K (2009) Transcriptional regulatory networks in response to abiotic stresses in Arabidopsis and grasses. Plant Physiol 149:88–95
Nelson DE, Repetti PP, Adams TR et al (2007) Plant nuclear factor Y (NF-Y) B subunits confer drought tolerance and lead to improved corn yields on water-limited acres. Proc Nat Acad Sci U S A 104:16450–16455
Nevo E, Chen G (2010) Drought and salt tolerances in wild relatives for wheat and barley improvement. Plant Cell Environ 32:670–685
Nevo E, Gorham J, Beiles A (1992) Variation for Na-22 uptake in wild emmer wheat, Triticum dicoccoides in Israel – salt tolerance resources for wheat improvement. J Exp Bot 43:511–518
Ortiz R, Iwanaga M, Reynolds MP et al (2007) Overview on crop genetic engineering for drought-prone environments. J SAT Agr Res 40:1–30
Park B-J, Liu Z, Kanno A et al (2005) Genetic improvement of Chinese cabbage for salt and drought tolerance by constitutive expression of a B. napus LEA gene. Plant Sci 169:553–558
Peleg Z, Fahima T, Abbo S et al (2005) Genetic diversity for drought resistance in wild emmer wheat and its ecogeographical associations. Plant Cell Environ 28:176–191
Pellegrineschi A, Reynolds M, Pacheco M et al (2004) Stress-induced expression in wheat of the Arabidopsis thaliana DREB1A gene delays water stress symptoms under greenhouse conditions. Genome 47:493–500
Qin F, Kakimoto M, Sakuma Y et al (2007) Regulation and functional analysis of ZmDREB2A in response to drought and heat stresses in Zea mays L. Plant J 50:54–69
Quan R, Shang M, Zhang H et al (2004) Engineering of enhanced glycine betaine synthesis improves drought tolerance in maize. Plant Biotechnol J 2:477–486
Reyes JL, Rodrigo M-J, Colmenero-Flores JM et al (2005) Hydrophilins from distant organisms can protect enzymatic activities from water limitation effects in vitro. Plant Cell Environ 28:709–718
Reynolds M, Dreccer F, Trethowan R (2007) Drought-adaptive traits derived from wheat wild relatives and landraces. J Exp Bot 58:177–186
Ribaut JM, Hoisington DA, Deutsch JA et al (1996) Identification of quantitative trait loci under drought conditions in tropical maize I. Flowering parameters and the anthesis-silking interval. Theor Appl Genet 92:905–914
Rivero RM, Kojima M, Gepstein A et al (2007) Delayed leaf senescence induces extreme drought tolerance in a flowering plant. Proc Nat Acad Sci U S A 104:19631–19636
Rivero RM, Shulaev V, Blumwald E (2009) Cytokinin-dependent photorespiration and the protection of photosynthesis during water deficit. Plant Physiol 150:1530–1540
Rohila JS, Rajinder K, Wu JR (2002) Genetic improvement of basmati rice for salt and drought tolerance by regulated expression of a barley Hva1 cDNA. Plant Sci 163:525–532
Rosenow DT, Dahlberg JA (2000) Collection, conversion and utilisation of sorghum. In: Smith CW, Frederiksen RA (eds) Sorghum, origin, history, technology and production. Wiley, New York
Sivamani E, Bahieldin A, Wraith JM et al (2000) Improved biomass productivity and water use efficiency under water deficit conditions in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci 155:1–9
Suprunova T, Krugman T, Fahima T et al (2004) Differential expression of dehydrin genes in wild barley, Hordeum spontaneum, associated with resistance to water deficit. Plant Cell Environ 27:1297–1308
Suprunova T, Krugman T, Distelfeld A et al (2007) Identification of a novel gene (Hsdr4) involved in water-stress tolerance in wild barley. Plant Mol Biol 64:17–34
Sutka J, Farshadfar E, Koszegi B et al (1995) Drought tolerance of disomic chromosome additions of Agropyron elongatum to Triticum aestivum. Cereal Res Commun 23:351–357
Toldi O, Tuba Z, Scott P (2009) Vegetative desiccation tolerance: is it a goldmine for bioengineering crops? Plant Sci 176:187–199
Trethowan RM, Mujeeb-Kazib A (2008) Novel germplasm resources for improving environmental stress tolerance of hexaploid wheat. Crop Sci 48:1255–1265
van de Wouw M, van Hintum T, Kik C et al (2010) Genetic diversity trends in twentieth century crop cultivars: a meta analysis. Theor Appl Genet 120:1241–1252
Wan J, Griffiths R, Yin J et al (2009) Development of drought-tolerant canola (Brassica napus L.) through genetic modulation of ABA-mediated stomatal responses. Crop Sci 49:1539–1554
Wang Y, Beaith M, Chalifoux M et al (2009) Shoot-specific down-regulation of protein farnesyltransferase (-subunit) for yield protection against drought in canola. Mol Plant 2:191–200
Warburton ML, Crossa J, Franco J et al (2006) Bringing wild relatives back into the family: recovering genetic diversity in CIMMYT improved wheat germplasm. Euphytica 149:289–301
Xiao B, Huang Y, Tang N et al (2007) Over-expression of a LEA gene in rice improves drought resistance under the field conditions. Theor Appl Genet 115:35–46
Xiao B, Chen X, Xiang C-B et al (2009) Evaluation of seven function-known candidate genes for their effects on improving drought resistance of transgenic rice under field conditions. Mol Plant 2:73–83
Xu DP, Duan XL, Wang BY et al (1996) Expression of a late embryogenesis abundant protein gene, HVA1, from barley confers tolerance to water deficit and salt stress in transgenic rice. Plant Physiol 110:249–257
Yadav OP (2008) Performance of landraces, exotic elite populations and their crosses in pearl millet (Pennisetum glaucum) in drought and non-drought conditions. Plant Breed 127:208–210
Yadav OP, Weltzien E (2000) Differential response of landrace-based populations and high yielding varieties of pearl millet in contrasting environments. Ann Arid Zone 39:39–45
Zare AG, Humphreys MW, Rogers JW et al (2002) Androgenesis in a Lolium multiflorum × Festuca arundinacea hybrid to generate genotypic variation for drought resistance. Euphytica 125:1–11
Zhang J-Y, Broeckling CD, Sumner LW et al (2007) Heterologous expression of two Medicago truncatula putative ERF transcription factor genes, WXP1 and WXP2, in Arabidopsis led to increased leaf wax accumulation and improved drought tolerance, but differential response in freezing tolerance. Plant Mol Biol 64:265–278
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Blum, A. (2011). Genetic Resources for Drought Resistance. In: Plant Breeding for Water-Limited Environments. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-7491-4_5
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