A comparison of monosomic and disomic substitution lines in the chromosomal location of leaf rust resistance genes in tetraploid wheats

dc.contributor.advisorSpies, J. J.
dc.contributor.advisorLabusehange, M. T.
dc.contributor.advisorPretorius, Z. A.
dc.contributor.authorAli, Shimelis Hussein
dc.date.accessioned2017-10-23T10:35:31Z
dc.date.available2017-10-23T10:35:31Z
dc.date.issued2003-05
dc.description.abstractEnglish: Two sets of aneuploids were employed and compared to localize adult plant leaf rust resistance genes in tetraploid wheat accessions. One set was the hexaploid Chinese Spring (CS) A- and B-genome monosomics (2n=6x-1=41, AABBDD) and the other the tetraploid Langdon durum D-genome disomie substitutions (2n=4x-2+2=28). The tetraploid accessions (2n=4x=28, AABB) 104 (Triticum turgidum subsp. dicoccum var. arras) and 127 (T. turgidum subsp. durum var. aestivum) were selected as leaf rust-resistant after evaluating 353 Triticum accessions. To study the chromosomal locations of the resistance genes, crosses were made between the complete sets of aneuploids (maternal parents) and the accessions. From both crosses F1 hybrids were used for meiotic chromosome analysis and to select monosomic plants for F2 segregation analysis. In the cross of the CS AB-genome monosomics with resistant lines, F1 monopentaploid plants (2n=5x-1=34, AABBD) were selected. In the other crosses of the resistant accessions with the substitution lines, F1 double monosomic plants were selected with 13 bivalent and two univalent chromosomes during metaphase I. The F2 segregates of selfed monosomic plants were inoculated at the flag leaf stage with pathotype UVPrt2 of Puccinia triticina. The CS monosomic analysis showed that in accession 104 a Lr gene occurs on chromosome 1A. Another gene in the accession was localized on chromosome 6B by Langdon durum substitution analysis. The second gene in this accession could not be localized from CS analysis since the F1 monopentaploid hybrid of that cross was sterile making the F2 segregation analysis incomplete. The gene localized on chromosome 1A in accession 104 by the CS analysis could not be localized by the substitution analysis owing to the presence of a suppressor gene brought from the 0 chromosome of substitution line 101 A. In accession 127 the resistance gene was located on chromosome 4A using the two sets of aneuploids. The study indicated that the tetraploid O-genome substitution lines are more commendable stocks than the hexaploid CS monosomics for chromosomal mapping of leaf rust resistance genes in tetraploid wheats. The trustworthiness of the tetraploid cytogenetic stocks is that the F1 double monosomic hybrids resulting from crossing with the tetraploid did not show sterility or poor germination. These would furnish complete F2 segregation analysis. Besides, the relatively few numbers of chromosomes in the F1 hybrids would ease meiotic chromosome analysis. However, it would be necessary to consider the CS monosomic stocks during gene interaction from D-genome chromosomes of certain substitution lines on genes present on the A- or B-genome chromosomes of the tetraploid wheat under study. The analysis of variance of important agronomic traits in the substitution lines suggested that three substitution aneuploids namely 202B, 707 A and 707B were phenotypically divergent when compared to the other lines and the recurrent parent. These lines are reportedly backcrossed for 12 generations to Langdon. It appears, however, that further backcrossings to the recurrent parent and further targeted selections are necessary to increase traits such as plant height, number of spikelets per spike, kernel weight, and seed yield in line 202B. The same selection schemes are required to improve the number of spikelets per spike, number of kernels per spike, kernel weight, and seed yield in line 707B. Additionally traits such as number of spikelets per spike, kernel weight and seed yield require further improvement in line 707 A. The path analysis revealed true associations of seed yield with kernel weight and heading date. This association was also supported by a simple correlation analysis. The direct path value of the path coefficient analysis exposed kernel weight as a key selection criterion to improve seed yield in the substitution aneuploids. The alternate path values further indicated selection for kernel weight would bring simultaneous selection of improved number of kernel per spike, spikelets per spike and plant height.en_ZA
dc.description.abstractAfrikaans: Twee aneuploïede reekse is vergelyk om volwasse blaarroesweerstandsgene in tetraploïede aanwinste te lokaliseer. Die reekse was die heksaploïede Chinese Spring (CS) A- en B-genoom monosome (2n=6x-1=41) en die tetraploïede Langdon durum D-genoom disomiese vervangingsreeks (2n=4x-2+2=28). Die tetraploïede koringaanwinste (2n=4x=28, AABB) beskryf as 104 (Triticum turgidum subsp. dicoccum var. arras) en 127 (T. turgidum subsp. durum var. aestivum), is geselekteer vir uitstekende blaarroesweerstand uit 353 Triticum aanwinste. Beide aneuploïede reekse is as moederplante gebruik in kruisings met die weerstandbiede stuifmeelouers om die chromosomale posisies van die Lr gene vas te stel. Meiotiese chromosoomanalises van die F1-basters is gebruik om monosomiese plante te selekteer vir die F2-segregasie analises. Monopentaploïede (2n=5x-1=34, AABBD) is geselekteer uit die kruising tussen CS AB-genoom monosome en die weerstandbiedende ouers. In die kruisings tussen die disomiese vervangingslyne en die weerstandbiede ouers, is dubbelmonosomiese F1-plante geselekteer met 13 bivalente en 2 univalente tydens metafase I. Selfbestuiwing van die geselekteerde monosome is tydens die vlagblaarstadium geïnokuleer met patotipe UVPrt2 van Puccinia triticina. Die CS monosoomanalises dui daarop dat die Lr-geen op chromosoom 1A geleë is in die kruising met aanwins 104. 'n Verdere geen op chromosoom 6B is waargeneem met die Landon durum vervangingslynanalise. Die tweede geen kon nie by die CS analise waargeneem word nie, omdat die F1- monopentaploïed steriel was en F2-segregasie-analise dus nie gedoen kon word nie. Die lokalisering van die Lr-geen op chromosoom 1A by aanwins 104 en CS monosoomanalise kon nie deur die vervangingsanalise bevestig word nie, moontlik weens onderdrukking van 'n ander Lr-geen. op die D-genoom chromosoom van die Langdon durum vervangingslyn, 1D(1A). Altwee reekse aneuploïdes vind die Lr-geen op chromosoom 4A in kruisings met aanwins 127. Hierdie studie toon dat chromosomale kartering van Lr gene in tetraploïede korings beter is met tetraploïede D-genoom vervangingslyne as sitogenetiese materiaal, as met die heksaploïede CS monosome. Die voordeel van die tetraploïede vervangingsmateriaal is dat die Fr-oubcelmonosome (die resultaat van die kruising met die tetraploïede korings) nie steriel is en geen ontkiemingsprobleme veroorsaak nie. 'n Volledige F2-segregasie-analise kan dus uitgevoer word. Daarbenewens bied die relatiewe lae chromosoomgetal van die Fj-basters 'n makliker meiotiese analise. "n Komplimentêre heksaploïede analise is slegs geregverdig indien die tetraploïede analise beïnvloed word deur geeninteraksie met die D-genoom. Die variansie-analise van belangrike agronomiese kenmerke in die vervangingslyne dui daarop dat die vervangingslynaneuploïdes, 2D2B, 707 A en 7D7B, fenotipies betekenisvol verskil van die ander lyne en die spilouer. Dit noodsaak herhaalde terugkruisings na die spilouer en verdere seleksies is nodig vir kenmerke soos planthoogte, aantal blompakkies per aar, saadmassa en saadopbrengs in lyn 2D2B. Dieselfde seleksieprosedure is nodig vir 'n verbetering in die aantal blompakkies per aar, aantal sade per aar, saadmassa, en saadopbrengs in lyn 7D7B. Kenmerke soos die aantal blompakkies per aar, saadmassa en saadopbrengs benodig verdere verbeterings in lyn 707 A. Baananalises dui aan dat saadopbrengs geassosieerd is met saadmassa en aarverskyning. Hierdie assosiasie word ondersteun deur 'n eenvoudige korrelasie analise. Die direkte baanwaarde van die baankoëffisiëntanalise dui op saadmassa as die sleutel seleksiemaatstaf vir die verbetering van saadopbrengs in die vervangingsaneuploïedes. Die alternatiewe baanwaardes dui daarop dat seleksie vir saadmassa gelyktydig seleksie vir die verbetering van aantal sade per aar, blompakkies per aar en planthoogte sal meebring.af
dc.identifier.urihttp://hdl.handle.net/11660/7333
dc.language.isoenen_ZA
dc.publisherUniversity of the Free Stateen_ZA
dc.rights.holderUniversity of the Free Stateen_ZA
dc.subjectLeaf rust of wheaten_ZA
dc.subjectWheat -- Diseases and pestsen_ZA
dc.subjectWheat -- Disease and pest resistanceen_ZA
dc.subjectThesis (Ph.D. (Plant Sciences))--University of the Free State, 2003en_ZA
dc.titleA comparison of monosomic and disomic substitution lines in the chromosomal location of leaf rust resistance genes in tetraploid wheatsen_ZA
dc.typeThesisen_ZA
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