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1.
Genetic resistance to broomrape (Orobanche cumana Wallr.) race F in sunflower line J1, derived from the wild perennial species Helianthusgrosseserratus Martens and Helianthus divaricatus L., has been reported to be controlled by dominant alleles at a single locus, Or6. However, deviations from this monogenic inheritance have been observed. The objective of the present study was to gain insight into the inheritance of resistance to broomrape race F in the sunflower line J1. F1, F2, F3 and BC generations from crosses between J1 and three susceptible lines, P21, NR5 and HA821 were evaluated. F1 hybrids showed both resistant (R) and moderately resistant (MR) plants, the latter having a maximum of five broomrape stalks per plant compared with >10 in the susceptible parents. This indicated incomplete dominance of the Or6 alleles. F2 plants were classified as R, MR or susceptible (more than five broomrape stalks per plant). Three different segregation ratios were observed: 3 : 1, 13 : 3 and 15 : 1 (R + MR : S), suggesting the presence of a second gene, Or7, whose expression was influenced by the environment. A digenic model was confirmed, based on the evaluation of F2:3 families.  相似文献   

2.
Interspecific hybrids and backcross generations between the wild perennial species Helianthus resinosus, Helianthus paucifiorus, Helianthus laevigatus, Helianthus nuttallii ssp. nuttallii T. & G. and Helianthus giganteus, resistant to broomrape (Orobanche cernua) and susceptible inbred lines were obtained to study crossability to cultivated sunflower and the transmission and expression of resistance to this parasitic weed. Conventional crosses with all the species tested were successful except for the crosses with diploid H. giganteus, for which embryo rescue techniques were needed to overcome hybrid incompatibility. Pollen viability and seed set were highest for F1 hybrids with hexaploid species and lowest for those with the diploid H. giganteus. We evaluated F1, BC1F1, some BC2F1 plants and the wild and cultivated parents. The wild species and interspecific hybrids were resistant to broomrape infection except for H. nuttallii, which showed segregation, indicating that the resistance is dominant. The crossability and resistance of F1, and back-cross generations of species with different ploidy levels indicate that the transfer of broomrape resistance to cultivated sunflower is feasible.  相似文献   

3.
P.K. Singh    G.R. Hughes 《Plant Breeding》2006,125(3):206-210
Tan spot of wheat is caused by the fungus Pyrenophora tritici‐repentis. On susceptible hosts, P. tritici‐repentis induces two phenotypically distinct symptoms, tan necrosis and chlorosis. This fungus produces several toxins that induce tan necrosis and chlorosis symptoms in susceptible cultivars. The objectives of this study were to determine the inheritance of insensitivity to necrosis‐inducing culture filtrate of P. tritici‐repentis, race 2, and to establish the relationship between the host reaction to culture filtrate and spore inoculation with respect to the necrosis component. The F1, F2, and BC1F1 plants and F2:8 lines of five crosses involving resistant wheat genotypes ‘Erik’, ‘Red Chief’, and line 86ISMN 2137 with susceptible cultivars ‘Glenlea’ and ‘Kenyon’ were studied. Plants were spore‐inoculated at the two‐leaf stage. Four days later, the newly emerged uninoculated third leaf was infiltrated with a culture filtrate of isolate Ptr 92–164 (race 2). Reactions to the spore inoculation and the culture filtrate were recorded 8 days after spore inoculation. The segregation observed in the F2 and BC1F1 generations and the F2:8 lines of all crosses indicated that a single recessive gene controlled insensitivity to necrosis caused by culture filtrate. This gene also controlled resistance to necrosis induced by spore inoculation.  相似文献   

4.
Sunflower lines RHA‐274, HA‐61 and RHA‐325 were studied for their resistance to race 330 of downy mildew (Plasmopara halstedii). The same inbred line, with normal (HA‐89) or sterile cytoplasm (cmsHA‐89) was used in all the crosses as susceptible parent, and, in each cross, only one genotype of the resistant parent was studied. The resistant‐to‐susceptible ratios obtained in the BC1 and F2 progenies from the crosses of the lines RHA‐274 and HA‐61 to cmsHA‐89 and HA‐89, respectively, suggested that, in each resistant line, two dominant genes are responsible for resistance to this downy mildew race. One of the genes (A) is epistatic to the other (B), and the recessive allele b in homozygosity is also epistatic to aa, with plants carrying aabb genotypes being resistant. Resistance to race 330 seemed to be controlled by two complementary genes in the sunflower inbred line RHA‐325, the dominant allele of one of them being present in cmsHA‐89. In the genotypes HA‐89 or cmsHA‐89, the existence of genes that modify the expected segregations following the crosses with resistant parents is proposed. It is concluded that, although major genes have been described as responsible for monogenic resistance to downy mildew, other types of regulation of this character, such as complementarity and epistatic relationships, do occur.  相似文献   

5.
The genetics of resistance of common vetch (Vicia sativa L.) to broomrape (Orobanche crenata Forsk.) was studied for two years by using the P1, P2, F1, BC1, BC2, F2 F3, and F4 generations obtained from crosses between resistant and susceptible lines. Resistant lines were selected by screening a world collection m a naturally infested plot. Resistance was tested both under field and greenhouse conditions. The best index to measure resistance was the number of emerged broomrapes per host plant. The results fit the additive-dominance model. The main component of the variation was additivity; dominance and interaction effects seemed to depend on the environment. When dominance is expressed, a low number is dominant over a high number of broomrapes per host plant.  相似文献   

6.
A set of 21 monosomic (2n ‐ 1) and the disomic (2n) lines of the ‘Chinese Spring’ cultivar were crossed with ‘Chirya‐3′, the CIMMYT synthetic wheat line which has been identified as highly resistant for Helminthosporium leaf blight disease (HLB), in order to locate the genes governing disease resistance. The F1 and segregating populations were challenged and screened against the most virulent pure mono‐conidial HLB isolate KL‐8 (Karnal, India). The F1 progenies of the crosses were found to be susceptible because of the recessive nature of resistance. The F2 progeny of the control cross (‘Chinese Spring’בChirya‐3’), segregated in the ratio of 1: 15 (resistant: susceptible), indicating that resistance to HLB was controlled by a pair of recessive genes. While the F2 progeny of 19 monosomic crosses segregated in the ratio of 1: 15 (resistant: susceptible), the progeny of the remaining two crosses, 7B and 7D, deviated significantly from the ratio, revealing that 7B and 7D were the critical chromosomes for resistance genes that were located one on each chromosome. Moreover, the critical lines, 7B and 7D, confirmed the digenic complementary recessive nature of gene action by fitting well with the overall pooled F2 segregation ratio of 13: 51 (resistant: susceptible) as expected for digenic complementary recessive resistance. The F3 segregation ratios of the critical crosses, based on their pooled F2 analysis, was estimated as 19: 32: 13 (non‐segregating susceptible: segregating as susceptible and resistant: non‐segregating resistant). F3 progenies when tested with these ratios showed goodness‐of‐fit, confirming that the two pairs of recessive resistance genes were located on chromosomes 7B and 7D.  相似文献   

7.
Sunflower downy mildew caused by Plasmopara halstedii is an important disease of sunflower capable of causing losses of more than 80% of production. Races 100, 300, 310, 330, 710, 703, 730 and770 of the fungus have been identified in Spain. Race 703, of high virulence, has been identified frequently in the northeast, while race 310 seems to occur over the south, the main sunflower growing region of the country. Oil sunflower lines RHA-274 and DM4 were studied for their resistance to races 310(RHA-274 and DM4) and 703 (DM4). In each cross, only one plant of the resistant parent was crossed to the inbred susceptible line HA-89 (or cmsHA-89).Plants from F2 and backcross(BC1F1 to susceptible parent)generations were evaluated for fungal sporulation on true leaves and/or cotyledons. The resistant-to-susceptible ratios obtained in the F2 and BC1F1 progenies from the crosses cmsHA-89 × RHA-274 and HA-89 × DM4suggested that one major gene in each line is responsible for resistance to race 703.The segregations of the progenies of the cross HA-89 × DM4 inoculated with race 703also fitted the ratios 1:1 and 3:1 (for BC1F1 and F2, respectively)corresponding to control of resistance by a single dominant gene. In RHA-274, the gene for resistance to race 310 was designated Pl 9, whereas Pl v is tentatively proposed to designate the gene in DM4 responsible for resistance to races310 and 703. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

8.
Inheritance of black leaf mold resistance in tomato   总被引:1,自引:0,他引:1  
Summary Inheritance of black leaf mold (BLM) (caused by Pseudocercospora fuligena) resistance was studied in four crosses involving two resistant Lycopersicon accessions (PI134417, L. hirsutum and PI254655, L. esculentum) and four susceptible Asian Vegetable Research and Development Center tomato lines (CLN657BC1F2-267-0-3-12-7, CL143-0-10-3-0-1-10, CLN698BC1F2-358-4-13 and CL5915-93D4-1-0-3). For each cross, six generations, i.e. P1, P2, F1, F2, BC1F1 and BC1F2 were evaluated following inoculations with isolate Pf-2 of P. fuligena. Chi-square analyses of the data based on the ratio of resistant to susceptible plants in the F2 in three of four crosses gave a good fit to a segregation ratio of 1 R : 15 S, and BC1F2 data in three of four crosses gave an acceptable fit to the segregation ratio of 1 R : 63 S. The results indicate that resistance to BLM may be conditioned by two recessive genes acting epistatically in both PI134417 and PI254655.  相似文献   

9.
This study was conducted to evaluate the types of gene action governing the inheritance of resistance to peanut bud necrosis disease (PBND) in populations derived from three crosses involving two resistant (ICGV 86388 and IC 10) and one susceptible (KK 60–1) peanut lines. Populations were composed of P1 P2, F1 F2, BC11, BC12, BC11S and BC12S. These populations were evaluated for PBND incidence in a farmer's field in Kalasin province in north‐east Thailand, where PBND is a recurring problem. Results showed variations between crosses in the relative contributions of different types of gene effect. The results indicate that multiple genes control the PBND resistance trait, and that the two resistant lines differ in some of these genes. As non‐additive gene effects are important in all three crosses, selection for low PBND incidence in these crosses would be more effective in later generations.  相似文献   

10.
Phytophthora drechsleri causes stem blight, which is one of the most serious diseases of pigeonpea. Eight races of this fungus have been identified, but the inheritance of resistance to all these races is not clear except for race P2. This study examined the inheritance of resistance to race ‘Kanpur’ (KPR) of P. drechsleri in eight crosses involving four resistant parents, viz.‘KPBR 80‐2‐1′, ‘KPBR 80‐2‐2′, ‘Hy 3C and ‘BDN 1′, and two susceptible parents, viz.‘Bahar’ and ‘PDA 10′. The reactions of the parental lines, and their F1, F2 and backcross generations were studied in an infected plot. In the F1 generation of all crosses, a susceptible reaction was observed that indicated dominance of susceptibility over resistance. The segregation pattern in F2 indicated that two homozygous recessive genes (pdr1pdr1pdr2pdr2) were responsible for imparting resistance in the parents, ‘KPBR 80‐2‐1’ and ‘KPBR 80‐2‐2′, and that a single homozygous recessive gene (pdrpdr) was responsible for resistance in the parents ‘Hy 3C and ‘BDN 1′. Therefore, ‘KPBR 80‐2‐1’ and ‘KPBR 80‐2‐2’ with two genes for resistance are better donors because the resistance transferred from them will be more durable compared with ‘Hy3C and ‘BDN1’ with only one gene for resistance.  相似文献   

11.
A total of sixty‐six germplasm lines were crossed with five CMS lines, where two belong to A4 cytoplasm, while other three belong to A2 cytoplasm. On the basis of pollen fertility test as well as good pod setting, of 330 hybrids, 34 restorer lines were observed in ICPA 2043 and 19 in ICPA 2092. Thirteen germplasm lines restored fertility in both the A4 CMS lines, viz. ICPA 2043 and ICPA 2092; however, none of the lines restored fertility in A2 CMS lines. For confirmation of result, restoration competence of identified lines tested subsequently 2 years at two different temperatures. The segregation patterns for fertility restoration studied in F2 and BC1F1 generations of selected ten crosses. Six crosses indicated the involvement of two major genes with recessive epistasis, three crosses confirmed dominant epistasis, and one cross indicated the involvement of duplicate recessive epistasis. The obtained results from this study will hasten the future three‐line breeding programme and lead the hybrid technology to the farmers' field with the better exploitation of CMS lines.  相似文献   

12.
A study was conducted under controlled environment conditions in a phytotron to determine the nature of the inheritance of resistance Helminthosporium leaf blight (HLB) in a synthetic hexaploid wheat line, ‘Chirya‐3’, against the isolate KL‐8 of Bipolaris sorokiniana from the major wheat growing region of India. Crosses were made between two susceptible lines ‘WH 147’ and ‘Chinese Spring’. Analyses of F1 and F2 populations of these two crosses (‘WH 147’בChirya‐3’ and ‘Chinese Spring’בChirya‐3’) showed that resistance against the isolate in ‘Chirya‐3’ was governed by two recessive genes functioning in a complementary interaction giving an F2 segregation pattern of 1 : 15 (resistant : susceptible). The segregation pattern of the resistant F2 progenies in F3 families from both crosses confirmed that two homozygous recessive genes were responsible for resistance to the isolate of Bipolaris sorokiniana in the synthetic line ‘Chirya‐3’. It is proposed that the genes be designated as hlbr1 and hlbr2.  相似文献   

13.
Six intervarietal crosses involving two resistant and three susceptible genotypes of mungbean were attempted with the objectives to determine the mode of inheritance of gene‐specific Mungbean Yellow Mosaic Virus (MYMV) resistance. An infector row technique along with artificial inoculation was used for evaluating parents, F1, F2 and F3 plants for MYMV resistance. Disease scoring for MYMV indicated that F1s were highly susceptible as were the susceptible parents while resistant parent exhibited resistant reaction. The F2 progeny segregated in the ratio of 9 S:3 MS:3 MR:1 R suggesting that the resistance was governed by digenic recessive genes (rm1 and rm2). When one gene (rm1) was present in the homozygous recessive condition in different plants, it conferred moderately susceptible (MS) reaction, whereas when other gene (rm2) was in homozygous condition, moderately resistant (MR) reaction was obvious. When both genes (rm1 and rm2) were present together in the homozygous recessive condition, resistant reaction (R) was observed. The F2 segregation explained on the basis of phenotypic expression was further confirmed by F3 segregation.  相似文献   

14.
Six blast‐resistant pearl millet genotypes, ICMB 93333, ICMB 97222, ICMR 06444, ICMR 06222, ICMR 11003 and IP 21187‐P1, were crossed with two susceptible genotypes, ICMB 95444 and ICMB 89111 to generate F1s, F2s and backcrosses, BC1P1 (susceptible parent × F1) and BC1P2 (resistant parent × F1) for inheritance study. The resistant genotypes were crossed among themselves in half diallel to generate F1s and F2s for test of allelism. The F1, F2 and backcross generations, and their parents were screened in a glasshouse against Magnaporthe grisea isolates Pg 45 and Pg 53. The reaction of the F1s, segregation pattern of F2s and BC1P1 derived from crosses involving two susceptible parents and six resistant parents revealed the presence of single dominant gene governing resistance in the resistant genotypes. No segregation for blast reaction was observed in the F2s derived from the crosses of resistant × resistant parents. The resistance reaction of these F2s indicated that single dominant gene conferring resistance in the six genotypes is allelic, that is same gene imparts blast resistance in these genotypes to M. grisea isolates.  相似文献   

15.
The objective of this work was to develop homozygous common bean lines carrying angular leaf spot resistance genes derived from the cultivars ‘Mexico 54’, ‘MAR 2’ and ‘BAT 332’ through marker‐assisted selection. Molecular markers SCAR OPN02890, RAPD OPE04500 and OPAO12950 linked to the resistance genes of ‘Mexico 54’, ‘MAR 2’ and ‘BAT 332’, respectively, were used in segregating backcross‐derived populations to selection. DNA fingerprinting was used to select homozygous BC2F3 and BC1F3 resistant plants genetically closer to the recurrent parent. Two homozygous BC2F2:3 and two and five BC1F2:3 families derived from ‘Ruda’ vs. ‘Mexico 54’ (RM), ‘MAR 2’ (RMA) and ‘BAT 332’ (RB) crosses were selected, respectively. After only one (RMA, RB) or two backcrosses (RM), five and eight BC1F3 lines derived from RMA and RB, respectively, and seven BC2F3 lines derived from RM, with 14.9–16.6, 16.9–18.6 and 9.3–11.1% of relative genetic distances to the recurrent parent were selected. This is the first report of lines resistant to angular leaf spot carrying genes of the cultivars ‘Mexico 54’, ‘MAR 2’ and ‘BAT 332’ developed with the aid of molecular markers.  相似文献   

16.
Summary Six chickpea lines resistant to Ascochyta rabiei (Pass.) Lab. were crossed to four susceptible cultivars. The hybrids were resistant in all the crosses except the crosses where resistant line BRG 8 was involved. Segregation pattern for diseases reaction in F2, BCP1, BCP2 and F3 generations in field and glasshouse conditions revealed that resistance to Ascochyta blight is under the control of a single dominant gene in EC 26446, PG 82-1, P 919, P 1252-1 and NEC 2451 while a recessive gene is responsible in BRG 8. Allelic tests indicated the presence of three independently segregating genes for resistance; one dominant gene in P 1215-1 and one in EC 26446 and PG 82-1, and a recessive one in BRG 8.Research paper No. 3600  相似文献   

17.
S. P. Mishra    A. N. Asthana  Lallan  Yadav 《Plant Breeding》1988,100(3):228-229
Inheritance of Cercospora leaf spot resistance in mungbean was studied in 20 crosses involving crosses of resistant × susceptible, resistant × resistant, susceptible × susceptible lines. 3:1 ratio was observed in all 14 F2s involving resistant × susceptible parents. The inheritance of Cercospora leaf spot resistance is thus controlled by a single recessive gene. Our results are contradictory to observations of Thaklk et al. (1977 a, b) who found monogenic dominant inheritance of Cercospora leaf spot resistance in mungbean.  相似文献   

18.
Inheritance of reaction to Pseudomonas lachrymans in pickling cucumber   总被引:2,自引:0,他引:2  
Summary Cucumber (Cucumis sativus) lines resistant to angular leafspot caused by Pseudomonas lachrymans react to an infection by developing necrotic lesions that lack the chlorotic halo characteristic of the susceptible reaction. The inheritance of the non-halo lesion reaction was studied in all possible crosses between resistant lines MSU 9402 and Gy 14A, and susceptible cultivars Wisc. SMR 18 and National Pickling. Genetic analysis of the F1, F2, backcross and F3 populations revealed that the non-halo lesion type, associated with resistance, was controlled by a single recessive gene, pl. This character appears to be an important component of resistance to P. lachrymans.  相似文献   

19.
Two transgenic Bt rice lines, KMD1 and KMD2, both containing a synthetic cry1Ab gene from Bt, were crossed with conventional rice varieties. The inheritance of resistance to SSB of KMD1 and KMD2was investigated through LSB and field examination of their progenies, e.g. F1, BC1 and F2 populations. In LSBs, 100.0% of newly hatched SSB larvae died on the second day after feeding on leaf tissues of F1 and GUS positive BC1 plants, of which the area of leaf tissues consumed by SSB is also similar to that of transgenic parents. These results imply that the resistance of Bt rice to SSB is dominantly controlled and could be easily exploited in hybrid rice production. Field evaluation showed that segregation ratios for SSB resistance to susceptibility in BC1 populations fit the ratio of 1:1, which was also confirmed by LSBs. However, in F2 populations, the ratio was significantly smaller than 3:1 for resistant to susceptible plants in all 6 indica × japonica (KMD1 and KMD2) crosses, though it fitted 3:1 in all 4 japonica × japonica crosses. The results implied that the resistance of Bt rice to SSB was controlled by a dominant gene which was present in a homozygous condition in both KMD1 and KMD2, but the inheritance could be affected by other factors. Assays for Cry1Ab protein showed that, in most crosses, the content of Cry1Ab is significantly higher in leaves of GUS positive F1, BC1 and F2 plants than that in transgenic Bt parent plants, which accounts for the high resistance observed in these plants to SSB. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

20.
The inheritance of resistance to dry root rot of chickpea caused by Rhizoctonia bataticola was studied. Parental F1 and F2 populations of two resistant and two susceptible parents, along with 49 F1 progenies of one of the resistant × susceptible crosses were rested for their reaction to dry root rot using the blotting-paper technique. All F, plants of the resistant × susceptible crosses were resistant; the F2 generation fitted a 3 resistant: 1 susceptible ratio indicating monogenic inheritance, with resistance dominant over susceptibility. F3 family segregation data confirmed the results. No segregation occurred among the progeny of resistant × resistant and susceptible × susceptible crosses.  相似文献   

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