Microclimatic stress and adaptive DNA differentiation in wild emmer wheat, Triticum dicoccoides

 Genetic diversity was examined by RAPD-PCR analysis in 118 registered individuals of wild emmer wheat, Triticum dicoccoides, from a microsite at Yehudiyya, northeast of the Sea of Galilee, Israel. The test involved two climatic microniches in the open oak-park forest of Quercus ithaburensis: (1) sunny between trees and (2) shady under the trees’ canopies. Comparisons were based on 97 loci amplified by 20 oligonucleotide primers. Significant genetic differentiations were found at single-, two- and multilocus structures between the neighbouring shady and sunny niches. These DNA polymorphisms appear to be associated with microclimatic stresses. The pronounced niche-effect on the significance of linkage disequilibrium and niche-specific linkage disequilibrium may suggest that natural selection directed the two-locus associations. The structure of the multilocus associations also mainly results from natural selection, and not by chance from population subdivision, or founder effects. These findings are largely parallel to the previous allozymic results at single-locus and multilocus levels. Both the DNA and the allozymic results suggest that microclimatic selection appears to play an important role in DNA differentiation as well as in protein polymophism. Received: 30 October 1998 / Accepted: 2 November 1998     

Climatic effects on microsatellite diversity in wild emmer wheat (Triticum dicoccoides) at the Yehudiyya microsite,Israel

Microsatellite (SSR) diversity at 28 loci comprising seven types of tandem dinucleotide repeated motifs was analyzed in 105 individual plants of wild emmer wheat, Triticum dicoccoides, from a microsite in Yehudiyya, northeast of the Sea of Galilee, Israel. The study area was less than 1000 m(2) and involved 12 paired plots distributed in a mosaic pattern. Each experiment involved very close (a few meters apart), but sharply divergent, microclimatic niches in the open park forest of Tabor oak: (1) sun, between trees, and (2) shade, under tree canopy. Significant microclimatic divergence characterized many loci displaying asymmetric and non-random distribution of repeat numbers. Niche-specific and niche-unique alleles and linkage disequilibria were found in the two sub-populations. Microsatellite diversity at both single- and two-locus levels is affected by microclimatic environment. The evidence reflects effects of ecological stresses and natural selection on SSR diversity, resulting presumably in adaptive structures.     

Genetic polymorphisms of α- and β-amylase isozymes in wild emmer wheat,Triticum dicoccoides,in Israel

Summary - and -amylase isozyme diversity was studied electrophoretically by thin-layer polyacrylamide gel isoelectrofocusing in the tetraploid wild emmer wheat, Triticum dicoccoides, the progenitor of all cultivated wheats. We analyzed 225 plants from 23 populations encompassing the ecological spectrum of T. dicoccoides in Israel. The results were as follows: (a) Band and multilocus genotype polymorphisms abound and vary within and between the four amylase components: malt, green (-amylases), and dry and germinating seeds (-amylases). (b) The number of bands of malt, green, and dry and germinating seeds were 20, 6, 11 and 13, respectively, generating 40, 6, 51, and 51 patterns or multilocus genotypes (MGP), respectively. The MGPs vary drastically within and between populations, from monomorphic in some populations with a single pattern to highly polymorphic ones, (c) Mean H _e values for malt, green, and germinating and dry seeds are 0.053, 0.055, 0.088, and 0.077, respectively; mean number of bands per individual was 11.8, 4.4, 7.6, and 4.0, respectively, (d) The percentages of 50 bands and 148 multilocus genotype patterns (MGP) (in parenthesis) were classified into widespread, sporadic, and localized: 84.4 (10.8), 8.9 (12.2), 6.7 (77.0), respectively. Notably, 89.2% of the patterns were not widespread, but sporadic and localized, (e) The mean value of genetic distances among populations (Nei's D) for the four amylase groups is D = 0.136, 0.175, 0.288 and 0.307, respectively, not displaying geographical correlates. (f) Most of the - and -amylase diversity is between populations (G _st = 68–75%). (g) Significant environmental correlates occur between either bands or patterns and climatic diversity (water and primarily temperature factors). (h) Significant associations of multilocus amylase bands occur across Israel. Like-wise, significant gametic phase disequilibria, D, occur within populations and are positively correlated with climatic variables, primarily that of temperature, (i) Discriminant analyses correctly classified (95–100%) the 23 wild emmer populations into their ecogeographical region and soil type. (j) Autocorrelation analysis showed that there is no correlation between bands and geographic distance and excluded migration as a major factor of amylase differentiation.These results suggest that diversifying climatic and edaphic natural selection rather than stochastisity or migration is the major evolutionary force driving amylase differentiation at both the single and multilocus levels. Furthermore, wild emmer harbors high levels of - and -amylase diversity both as single bands and as multilocus adaptive genetic patterns. These are exploitable both as genetic markers for quantitative loci (QTLs) and as adaptive genetic resources to improve wheat germination and growth through classical breeding and/or biotechnology.     

Microgeographic edaphic differentiation in allozyme polymorphisms of wild barley (Hordeum spontaneum,Poaceae)

Allozymic variation in proteins encoded by 22 loci was analyzed electrophoretically in 278 individual plants of wild barley,Hordeum spontaneum, the progenitor of cultivated barley, in four 100 meter transects, in Israel, each equally subdivided into basalt and terra rossa soil types. Significant differentiation according to soil was found in 9 alleles. Our results suggest that allozyme polymorphisms in wild barley are at least partly adaptive, and differentiate by edaphic natural selection rather than by stochastic processes, and/or neutrality of allozymic variants.     

Adaptive microgeographic differentiation of allozyme polymorphism in landsnails

To elucidate the forees maintaining protein polymorphisms, microgeographic differentiation in proteins, encoded by 30 loci, was tested in 285 individuals comprising 3 species of landsnails in Israel. Each test consisted of 2 close subpopulations: one from the drier and warmer south-facing slope and the other from the opposite wetter and cooler north-facing slope. The 5 tests involved 2 of Buliminus labrosus in Mediterranean Count Carmel; 1 of Sphincterochila zonata in the northern, and 2 of S. prophetarum in the central Negev desert. The results indicate significant allele differences between the two slopes in several loci in each of the 5 local tests, involving primarily esterases (Est), aspartate aminotransferase (Aat) and leucine amino peptidases (Lap). The differential slope patterns appear to be adaptive, and are presumably maintained by microclimatic diversifying selection.     

Protein resources in wild barley,Hordeum spontaneum,in Israel: Predictive method by ecology and allozyme markers

Geographic variation in protein content of wild barley,Hordeum spontaneum, and the associations of protein content with ecological and allozyme markers were tested in an attempt to derive predictive guidelines for conservation and utilization in breeding programs. The study involved 195 genotypes of wild barley from 25 populations, 15 central and 10 marginal. These populations had been tested earlier for allozymic variation (Nevo & al. 1979 a, b). The results indicate that protein content varies both within, but particularly between populations. Notably, the 10 marginal populations exhibit high protein content but low kernel weight, as compared with the 15 central populations which displayed lower protein content but high kernel weight. Three variable combinations of climatic factors explain 40% of the variability in protein content among populations. Likewise, 3 variable combinations of allozyme allele frequencies explain a significant degree of spatial variance in protein content (R square = 0.63). — We conclude that natural populations of wild barley in Israel contain large amounts of yet untapped genes for protein content. These could be effectively screened and utilized for producing high protein cultivars of barley by following ecological and allozymic markers as predictive guidelines in screening natural populations of wild barley.     

NATURAL SELECTION OF ALLOZYME POLYMORPHISMS: A MICROSITE TEST REVEALING ECOLOGICAL GENETIC DIFFERENTIATION IN WILD BARLEY

Allozymic variation in proteins encoded by 25 loci was analyzed electrophoretically in 1982 and 1983 in 356 individual plants from a dense population of wild barley, Hordeum spontaneum, the progenitor of cultivated barley. The test involved six microniches organized in a mosaic pattern in the open Tabor oak forest at Neve Ya'ar, Israel. The microniches were i) sun-soil, ii) sun-rock, iii) shade-soil, iv) shade-rock, and the contact zones: v) soil periphery of the sun-rock microniche, and vi) soil periphery of the shade-rock microniche. Discriminant analysis indicated significant multilocus allozymic differentiation between the microniches. Our results suggest that allozyme polymorphisms in wild barley are at least partly adaptive and differentiate predominately by microniche ecological selection, rather than by stochastic processes and/or neutrality of allozymic variants.     

Genetic resources of wild barley in the Near East: structure, evolution and application in breeding

Genetic diversity and structure of populations of the wild progenitor of barley, Hordeum spontaneum, from three countries, Israel, Turkey and Iran, in the Near East Fertile Crescent, are compared and contrasted. The analysis is based on electrophoretically discernible allozymic variation in proteins encoded by 27 shared loci in 2125 individuals representing 52 populations of wild barley. The results indicate that: (a) H. spontaneum in the Near East Fertile Crescent is very variable genetically; (b) genetic differentiation of populations includes some clinal but primarily regional and local patterns often displaying sharp geographic differentiation over short distances; (c) the average relative genetic differentiation (G_st) was 54% within populations, 39% among populations, and 8% between the three countries; (d) allele distribution is characterized by a high proportion of unique alleles (51%), and a high proportion of common alleles that are distributed either locally or sporadically; (e) discriminant analysis by allele frequencies successfully clustered wild barley of each of the three countries (96% correct classification); (f) a substantial portion of the patterns of allozyme variation in the wild gene pool is significantly correlated with the environment and is predictable ecologically, chiefly by a combination of humidity and temperature variables; (g) natural populations of wild barley are, on the average, more variable than two composite crosses and land races of cultivated barley. The spatial patterns and environmental correlates and predictors of genetic variation of H, spontaneum in the Fertile Crescent indicate that genetic variation in wild barley populations is not only rich but at least partly adaptive and predictable by ecology and allozyme markers. Consequently, conservation and utilization programmes should optimize sampling strategies by following the ecological-genetic factors and allozyme markers as effectively predictive guidelines.