Genetic and cytogenetic analyses of the A genome of Triticum monococcum L. V. Inheritance and linkage relationships of genes determining the expression of 12 qualitative characters

Genome ◽  
1989 ◽  
Vol 32 (5) ◽  
pp. 869-881 ◽  
Author(s):  
J. Kuspira ◽  
J. Maclagan ◽  
R. N. Bhambhani ◽  
R. S. Sadasivaiah ◽  
N.-S. Kim

Our investigation of 460 true-breeding lines confirms a long-standing observation that natural phenotypic and genetic variability in the diploid wheat Triticum monococcum L. is limited. The modes of inheritance of 12 morphological characters are discussed in light of the extensive information available on the genetics and cytogenetics of many of these characters in the related wheat Triticum aestivum. Analysis of data from appropriate crosses, complementation studies, and observations of phenotypes of F1s and F2s from crosses between lines expressing dominant traits indicate that each of these characters is determined by one major gene. A multiple allelic series exists at each of the Hg (glume pubescence) and Hn (node pubescence) loci. The genes for six of these characters fall into two closely linked groups. Genes Bg (glume colour) and Hg are the same distance apart as in Triticum aestivum, indicating that at least this segment of chromosome 1A has been highly or completely conserved since the origin of the polyploid wheats. The genes Sg (glume hardness), La (lemma awn length), Fg (false glume), and Lh (head type) are also very closely linked, with the outside markers being only 4 map units apart. The dominant and recessive alleles of genes determining these characters should serve as excellent markers for linkage and chromosomal mapping because of their complete penetrance and constant expressivity. Tentative assignments of genes and linkage groups identified in this investigation to specific chromosomes of T. monococcum have been made on the basis of known chromosomal locations of A genome genes in T. aestivum. The tentative assignments could be verified using a variety of genetic and cytogenetic approaches. It is suggested that a thorough study of the genetic heritage of einkorn wheat will require the use of induced mutants since natural genetic variability is low in this species.Key words: Triticum, characters, inheritance, linkage, mapping, A genome.

1986 ◽  
Vol 28 (1) ◽  
pp. 88-95 ◽  
Author(s):  
J. Kuspira ◽  
J. Maclagan ◽  
K. Kerby ◽  
R. N. Bhambhani

The study on the mode of inheritance of spring versus winter growth habit in Triticum monococcum is the first in a diploid wheat species. The results are discussed in light of the information available on the genetics and cytogenetics of this character in Triticum aestivum. Two spring habit and six winter habit lines were used in these investigations. Statistical analyses of progenies in each of these lines clearly established the true-breeding nature of all eight lines with respect to days to heading. Analysis of F1 and F2 results of crosses between the two spring habit lines 68 and 293 showed the following: (i) neither line carries winter habit alleles at any of the major gene loci determining growth habit; and (ii) four of five minor allele pairs determine the phenotypic differences between them. Monohybrid F2 and testcross ratios in crosses between spring habit line 68 and each of the six winter lines lead to the following conclusions: (i) differences between spring and winter growth habit in each cross are due to alleles of one major gene; (ii) the allele for spring habit is completely dominant to that for winter habit in each cross; and (iii) all these lines are genotypically identical or very similar at all modifying gene loci. These results imply that only one major gene determines growth habit in this species. Diallel (critical) crosses among the six recessive lines indicate that complementation does not occur in any of the F1's. Therefore, all these recessive genes represent mutations in the same gene. If these results are characteristic of all winter lines in Triticum monococcum, they permit the initial conclusion that only one major gene determines growth habit in this diploid species. This locus is in all likelihood the VrnI locus since it is the only one of the five major genes identified for growth habit, that is present in the A genome of Triticum aestivum. All six recessive lines respond to natural vernalization. This lends further support to our initial conclusion. Because the six recessive lines head at five different times we conclude that a multiple allelic series occurs at this locus. Specifically, at least three and probably five recessive alleles responsible for different heading dates among the winter lines, and at least one dominant allele for spring habit, occur at this locus.Key words: Triticum, complementation, quantitative, vernalization, alleles, multiple.


2021 ◽  
Author(s):  
Hammouda Bousbia Dounia ◽  
Benbelkacem Abdelkader

The distribution and Caracterization of constitutive heterochromatin in A-Am genomes of diploid wheat (progenitor), polyploid wheat (hybrids) and triticales (primary and secondary) are analyzed and compared by C-bands. The Comparison of zones rich in highly repeated DNA sequences marked by C bands on the all chromosomes of Am - A genomes revealed an important structural heterogeneity. Four chromosomes of Triticum monococcum (1Am-3Am-4Am-5Am) are almost similar to their homologues in wheat (Triticum durum , Triticum aestivum ) and triticale, by the presence or absence of C bands. Contrary to the chromosomes 2Am (rich in heterochromatin), 6Am-7Am (absence of C bands) show a great differentiation compared to their homologues of Triticum durum and Triticum aestivum and x-Triticosecale Wittmack. In the triticales, A genome chromosomes are richer in heterochromatin compared to theirs homologous of polyploid wheats. This is explained by a "genome shock The confrontation of C- bands genome (Triticum monococcum) with a C+ bands genome (durum wheat / or common wheat) produces an interspecific hybrid which at the sixth generation reveals C+ bands (triticales). The variations observed in our vegetal material indicated the existence of an intervarietal and interspecific heterochromatic polymorphism. The presence of B chromosomes in triticales, could be explained as a manifestation of their adaptation.


2010 ◽  
Vol 123 (4) ◽  
pp. 1267-1274 ◽  
Author(s):  
Kateřina Hejtmánková ◽  
Jaromír Lachman ◽  
Alena Hejtmánková ◽  
Vladimír Pivec ◽  
Dagmar Janovská

Genome ◽  
1987 ◽  
Vol 29 (5) ◽  
pp. 722-737 ◽  
Author(s):  
K. Kerby ◽  
J. Kuspira

The phylogeny of the polyploid wheats has been the subject of intense research and speculation during the past 70 years. Various experimental approaches have been employed to ascertain the diploid progenitors of these wheats. The species having donated the D genome to Triticum aestivum has been unequivocally identified as Aegilops squarrosa. On the basis of evidence from many studies, Triticum monococcum has been implicated as the source of the A genome in both Triticum turgidum and Triticum aestivum. However, numerous studies since 1968 have shown that Triticum urartu is very closely related to Triticum monococcum and that it also carries the A genome. These studies have prompted the speculation that Triticum urartu may be the donor of this chromosome set to the polyploid wheats. The donor of the B genome to Triticum turgidum and Triticum aestivum remains equivocal and controversial. Six different diploid species have been implicated as putative B genome donors: Aegilops bicornis, Aegilops longissima, Aegilops searsii, Aegilops sharonensis, Aegilops speltoides, and Triticum urartu. Until recently, evidence presented by different researchers had not permitted an unequivocal identification of the progenitor of the B genome in polyploid wheats. Recent studies, involving all diploid and polyploid wheats and putative B genome donors, lead to the conclusion that Aegilops speltoides and Triticum urartu can be excluded as B genome donors and that Aegilops searsii is the most likely source of this chromosome set. The possibility of the B genome having arisen from an AAAA autotetraploid or having a polyphyletic origin is discussed. Key words: phylogeny; Triticum aestivum; Triticum turgidum; A, B, and D genomes.


Author(s):  
Shisheng Chen ◽  
Joshua Hegarty ◽  
Tao Shen ◽  
Lei Hua ◽  
Hongna Li ◽  
...  

AbstractKey messageThe stripe rust resistance geneYr34 was transferred to polyploid wheat chromosome 5AL from T. monococcumand has been used for over two centuries.Wheat stripe (or yellow) rust, caused by Puccinia striiformis f. sp. tritici (Pst), is currently among the most damaging fungal diseases of wheat worldwide. In this study, we report that the stripe rust resistance gene Yr34 (synonym Yr48) is located within a distal segment of the cultivated Triticum monococcum subsp. monococcum chromosome 5AmL translocated to chromosome 5AL in polyploid wheat. The diploid wheat species Triticum monococcum (genome AmAm) is closely related to T. urartu (donor of the A genome to polyploid wheat) and has good levels of resistance against the stripe rust pathogen. When present in hexaploid wheat, the T. monococcum Yr34 resistance gene confers a moderate level of resistance against virulent Pst races present in California and the virulent Chinese race CYR34. In a survey of 1,442 common wheat genotypes, we identified 5AmL translocations of fourteen different lengths in 17.5% of the accessions, with higher frequencies in Europe than in other continents. The old European wheat variety “Mediterranean” was identified as a putative source of this translocation, suggesting that Yr34 has been used for over 200 years. Finally, we designed diagnostic CAPS and sequenced-based markers that will be useful to accelerate the deployment of Yr34 in wheat breeding programs to improve resistance to this devastating pathogen.


Genome ◽  
2004 ◽  
Vol 47 (5) ◽  
pp. 789-794 ◽  
Author(s):  
M Razavi ◽  
G R Hughes

This study examined the genetic structure of a Saskatchewan population of Mycosphaerella graminicola, cause of the foliar disease Septoria tritici blotch of wheat. Such knowledge is valuable for understanding the evolutionary potential of this pathogen and for developing control strategies based on host resistance. Nine pairs of single-locus microsatellite primers were used to analyze the genomic DNA of 90 isolates of M. graminicola that were collected using a hierarchical sampling procedure from different locations, leaves, and lesions within a wheat field near Saskatoon. Allelic series at eight different loci were detected. The number of alleles per locus ranged from one to five with an average of three alleles per locus. Genetic diversity values ranged from 0.04 to 0.67. Partitioning the total genetic variability into within- and among-location components revealed that 88% of the genetic variability occurred within locations, i.e., within areas of 1 m2, but relatively little variability occurred among locations. Low variability among locations and a high degree of variability within locations would result if the primary source of inoculum was airborne ascospores, which would be dispersed uniformly within the field. This finding was confirmed by gametic disequilibrium analysis and suggests that the sexual reproduction of M. graminicola occurs in Saskatchewan.Key words: Mycosphaerella graminicola, SSR markers, sexual reproduction, genetic diversity.


2021 ◽  
Vol 52 (1) ◽  
pp. 177-197
Author(s):  
Brian Charlesworth ◽  
Jeffrey D. Jensen

Patterns of variation and evolution at a given site in a genome can be strongly influenced by the effects of selection at genetically linked sites. In particular, the recombination rates of genomic regions correlate with their amount of within-population genetic variability, the degree to which the frequency distributions of DNA sequence variants differ from their neutral expectations, and the levels of adaptation of their functional components. We review the major population genetic processes that are thought to lead to these patterns, focusing on their effects on patterns of variability: selective sweeps, background selection, associative overdominance, and Hill–Robertson interference among deleterious mutations. We emphasize the difficulties in distinguishing among the footprints of these processes and disentangling them from the effects of purely demographic factors such as population size changes. We also discuss how interactions between selective and demographic processes can significantly affect patterns of variability within genomes.


2002 ◽  
Vol 93 (3) ◽  
pp. 1000-1006 ◽  
Author(s):  
Mary F. Feitosa ◽  
Steven E. Gaskill ◽  
Treva Rice ◽  
Tuomo Rankinen ◽  
Claude Bouchard ◽  
...  

This study investigates whether there are major gene effects on oxygen uptake at the ventilatory threshold (V˙o 2 VT) and theV˙o 2 VT maximal oxygen uptake (VT%V˙o 2 max), at baseline and in response to 20 wk of exercise training by using data on 336 whites and 160 blacks. Segregation analysis was performed on the residuals ofV˙o 2 VT and VT%V˙o 2 max. In whites, there was strong evidence of a major gene, with 3 and 2% of the sample in the upper distribution, that accounted for 52 and 43% of the variance in baseline V˙o 2 VT and VT%V˙o 2 max, respectively. There were no genotype-specific covariate effects (sex, age, weight, fat mass, and fat-free mass). The segregation results were inconclusive for the training response in whites, and for the baseline and training response in blacks, probably due to insufficient power because of reduced sample sizes or smaller gene effect or both. The strength of the genetic evidence for V˙o 2 VT and VT%V˙o 2 max suggests that these traits should be further investigated for potential relations with specific candidate genes, if they can be identified, and explored through a genome-wide scan.


Biologia ◽  
2011 ◽  
Vol 66 (1) ◽  
Author(s):  
Tariq Mahmood ◽  
Anna Iqbal ◽  
Nazia Nazar ◽  
Ishrat Naveed ◽  
Bilal Abbasi ◽  
...  

AbstractFamily Apocynaceae is an economically important family grown as ornamental plants and many wild species have medicinal uses as well. The aim of the present study was to understand the level and pattern of genetic variability among the selected individuals of Apocynaceae. For this purpose, three species of different genera of Apocynaceae, Thevetia peruviana, Alstonia scholaris and Catharanthus roseus, were collected from Rawalpindi and Quaid-i-Azam University forest, Islamabad. To evaluate the level of polymorphism within the species and members of different species, randomly amplified polymorphic DNA (RAPD) markers were used. A series of OPC RAPD primers were used; only six primers of OPC series gave amplification. Highest genetic variation at interspecific and intraspecific levels was shown by OPC 9 and the lowest polymorphism was observed in OPC 4. The data was analyzed by using software Statistica 5.5. In total 105 monomorphic and 272 polymorphic bands were produced from all primers. Therefore, out of 322 amplified products, 26% were monomorphic and 68% were polymorphic. Low genetic diversification was observed both at intraspecific and interspecific level. At the molecular level Alstonia scholaris and Catharanthus roseus (subfamily Plumerioideae) appeared in a group and Thevetia peruviana (subfamily Rauvolfoideae) formed another group, confirming the classification based on morphological characters.


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