Seasonal changes in the incidence of apomixis of diploid,triploid, and tetraploid plants of Paspalum cromyorrhizon

Summary Changes in incidence of apomixis were determined at different intervals of the flowering period in a highly sexual diploid cytotype of Paspalum cromyorrhizon Trin., a natural tetraploid cytotype of the same species, and in the triploid and tetraploid intraspecific hybrids that were produced by pollinating the 2x cytotype with pollen of the tetraploid. Reproductive behaviour was determined from observations of embryo sacs in mature ovules. Gametophytic apomixis in this species in characterized by aposporous embryo sacs which differ from normal sacs by their number, orientation inside the ovule, their dimensions and shape, and the absence of antipodal cells.The potential for apomictic reproduction increased in relation to the ploidy level, suggesting a gene dosage effect in the incidence of apomixis. In the three ploidy levels, the highest incidence of apomixis was observed when the plants reached the maximum number of flowering heads. These findings suggest that the same environmental conditions that favour flowering should also be responsible for increasing the incidence of apomixis. An additional experiment under controlled conditions indicated that the light regime should be one of the factors that govern the amount of apomictic reproduction. Thus, polyploidy and apomixis should be of special significance in the dispersion and evolution of this grass species. The 4x facultative apomictic cytotype is far more frequent in nature than the highly sexual 2x. Moreover, most of the seeds produced in a flowering season should arise asexually. So, apomixis rapidly increases the number of plants bearing the successful maternal genotype, and sexual reproduction becomes important in adverse environmental conditions.     

Second cycle gynogenesis in onion, Allium cepa L., and genetic analysis of the plants

Haploid induction in onion via gynogenesis provides inbred lines that can be used in production of hybrid cultivars. Despite several successful reports, the gynogenic induction rate is still relatively low, ranging mainly from 0.5 to six embryos per 100 cultured flowers. In the present study, gynogenesis was induced in selfed progeny of three genetically homozygous and stable fertile doubled haploid lines previously obtained through in vitro gynogenesis. The aims were to acquire information on whether the gynogenic responsiveness of a particular heterozygous cultivar is correlated with higher or lower gynogenic capacity in the second cycle of gynogenesis, to evaluate the non-genetic component of the variability, and to monitor by random amplified polymorphic DNA (RAPD) analysis the onset of eventual gametoclonal variation induced during the gynogenic processes. The results from the gynogenic induction of 9708 flowers showed significant differences among three lines, one of them being extremely responsive, showing a mean yield of 118.3 haploid embryos per 100 cultured flowers (118.3%). The high embryo yield of this line was determined by the line's particular genotype. However, the induction rate of gynogenic embryos obtained within 24 genetically uniform donor plants of this responsive line varied from 67 to 196% and this variation can be attributed to uncontrolled environmental conditions. A total of 157 plants sampled from two lines and obtained through a first (RI) and a second (SCG) cycle of gynogenesis, was analysed by RAPDs. The single band profiles were compared either between or within the RI and SCG plants of each line. A total number of 4600 RAPD fragments were scored and no variation was found in the highly responsive line, while in the less responsive one, minor changes were detected for the presence/absence of two RAPD bands. These results indicate high genetic stability of onion homozygous lines passed through two cycles of gynogenesis.     

An estimation of homogeneity in crop plants,with special reference to genetic vulnerability in the dry bean,Phaseolus vulgaris L.

Summary A general method of quantitatively assessing genetic similarity among a set of cultivars of a given crop is proposed, and its application to dry beans in the United States is demonstrated. The method is based upon the multi-variate technique of Principal Components Analysis. Using this method it was possible to calculate a distance metric between any two cultivars in the set and to show that such distances were highly inversely correlated with genetic relationship estimated from a knowledge of breeding ancestry.On the basis of distances among cultivars within given production regions (states in the US in this case) and knowledge of the acres of each cultivar grown in the region, an average weighted distance metric appropriate to each was calculated. Each derived distance metric serves as an index of genetic homogeneity for the crop in that region. Arguments are presented for relating the degree of vulnerability to a disease epidemic to the distance index. Indexes are calculated for nine of the major bean producing states in the US from which it is concluded that, from the standpoint of genetic vulnerability, Colorado is most vulnerable and California least vulnerable to a region-wide epidemic affecting the bean crop. It is suggested that the method demonstrated here is of nearly universal applicability, and particularly meaningful with respect to self-fertilizing crops.     

A genetic analysis of the number of cells,length of cell,and gibberellic acid sensitivity in sugar beet and their relation to bolting mechanism

Summary Three series of full-sib progenies and parental inbred lines or populations were used to study the inheritance of the number of cells and length of cell along the hypocotyl length, and the response to gibberellic acid in young plants of sugar beet. Variance components were determined by using a factorial cross design. There were no significant estimates of non-additive genetic variation for either cellular characters. Both additive and non-additive genetic variance were responsible for the variability of stem length after GA3 treatment. It is concluded that additive type genes predominantly control the number of cells in all series. The length of cell had significant additive variances in most cases, but it was indeed markedly influenced by environmental factors. Number of cells (cell division rate) and GA3 sensitivity in young plants even before vernalization were related to bolting tendency. Bolting-susceptible genotypes generally expressed higher stem length in the response to added GA3 as compared to the bolting-resistant genotypes. However, some genotypes bolted easily in the field but reacted weakly to the GA3 treatment and vise versa. Genotypes that were susceptible to bolting and/or sensitive to GA3 had a specific range (intermediate) of cell number. There were, however, some genotypes containing an intermediate number of cells which demonstrated low bolting. These responded faintly to gibberellin treatment. The results suggest that several physiological requirements have to be fulfilled before bolting can occur, and that other plant characters interfere with the bolting phenomenon.     

Introgression of Xa4, Xa7 and Xa21 for resistance to bacterial blight in thermosensitive genetic male sterile rice (Oryza sativa L.) for the development of two-line hybrids

Bacterial blight (BB) of rice caused by X. oryzae pv. oryzae is a major production constraint in commercial hybrid rice production in the Philippines because most of the parental lines used in hybrid production do not carry resistance genes against the pathogen. In this study, three bacterial blight resistance genes, Xa4, Xa7 and Xa21, were introgressed to a temperature-sensitive genetic male sterile (TGMS1) line. A three-way cross of AR32-19-3-3/TGMS1//IRBB4/7 (PR36944) was made to produce 1,364 F₂ plants carrying various combinations of Xa4, Xa7 and Xa21. Individual plants were characterized for reaction to bacterial blight PXO61 (race 1), PXO86 (race 2), PXO99 (race 6) and pollen sterility. Of 144 F₂ plants demonstrating resistance against PXO61, PXO86 and PXO99, 22 exhibited highly resistant phenotypes with mean lesion lengths ranging from 0.37–2.97 cm. Analysis of disease reaction identified 20 potential TGMS F₂ plants containing Xa4, Xa7 and Xa21 while 78 plants with Xa4 + Xa7. Phenotypic and polymerase chain reaction (PCR) analyses confirmed PR36944-450, PR36944-473 and PR36944-700 as homozygous for Xa7 and Xa21 and highly resistant to all three Xoo races. Fertility of PR36944-450 and PR36944-700 was restored at permissive temperature in a growth chamber. BB-resistant TGMS lines should facilitate breeding two-line hybrids in the tropics.