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1.
Summary Experiments were made to ascertain whether sex expression in the onion depends on temperature.Some populations were found to be largely male sterile at about 14°C and much less so at 20°–23°C. In other populations this phenomenon did not occur. Besides all the fertile populations produced less and worse pollen at 14°C.The first-mentioned temperature influence may be an essential factor in searching for an explanation for the partially male sterile plants found by various research workers, and for the unexpected segregations for male sterility when A-, B- and C-lines are propagated.  相似文献   

2.
Development of cytoplasmic-genic male sterility in safflower   总被引:1,自引:0,他引:1  
K. Anhani 《Plant Breeding》2005,124(3):310-312
An interspecific cross was made between Carthamaus oxyacantha and the cultivated species C. tinctorius to develop a cytoplasmic‐genic male sterility (CMS) system in safflower. C. oxyacantha was the donor of sterile cytoplasm. The 3: 1 segregation pattern observed in BC1F2 suggested single gene control with dominance of male‐fertility over male‐sterility. The information obtained from crossing male sterile X male fertile plants in BC1F3 and BC1F4 generations showed statistically significant single gene (1: 1) segregation for male sterility vs. male fertility. The results demonstrated that C. tinctorius possesses a nuclear fertility restorer gene and that a single dominant allele restored fertility (Rf) in progeny carrying CMS cytoplasm of C. oxyacantha. Male sterility occurred with the homozygous recessive condition (rfrf) in a sterile C. oxyacantha cytoplasm background and not in the normal cytoplasm of C. tinctorius. The genetic background of different restorer lines of C. tinctorius having normal cytoplasm did not effect fertility restoration. The absence of male sterile plants in C. tinctorius populations ruled out the possibility of genetic male sterility. Normal meiosis in F1 and BC1F2 ruled out a cytogenetic basis for the occurrence of male sterility.  相似文献   

3.
Summary The male sterility system MS-1 of Brassica oleracea was studied in order to elucidate if nucleo-cytoplasmic interactions determine this system. Crosses of male sterile MS-1 genotypes with heterozygous MS-5 genotypes gave fully fertile F1 progenies. Selfing of seven F1 plants resulted in five F2 populations showing a 9:7 segregation ratio and two a 3:1 ratio for fertile and male sterile plants. Two F2 progenies deviated from the expected 9:7 or 3:1 segregation ratios for fertile and male sterile plants. Thermosensitivity and distortion of the meiosis are suggested as the causal factors underlying the deviation of the segregation ratios. It was concluded that nuclear factors determine the male sterility in the MS-1 system, because the presence of a nucleocytoplasmic interaction in this system should have given only a 3:1 segregation ratio for fertile and male sterile plants in the F2 generation.  相似文献   

4.
Summary A high frequency of male sterile mutants regeneration was shown in callus cultures derived from leaves and panicles of haploid sorghum (Msc1, A1 cytoplasm) and a spontaneous autodiploid obtained from this haploid. The cultures derived from the embryos of this autodiploid yielded significantly fewer mutants. Absolutely or partially male sterile mutants appeared among the regenerants or in the progeny of fertile regenerants. In the self-fertilized progenies of partially male sterile mutants and in the hybrids of sterile mutants with autodiploid line (i.e. under one and the same nuclear genome) male sterility mutations were inherited as cytoplasmic. Non-Mendelian segregation of sterile, partially male sterile and fertile plants was observed in these progenies. Partially male sterile plants were characterized by somatic segregation of male sterility genetic factors. In test-crosses with some CMS A1 fertility restorers, mutations were manifested as nuclear recessive while with others as nuclear dominant. These differences are supposed to be the result of interaction of fertility restorer genes of these testers with the novel cytoplasm. Male sterility mutations accompanied with female sterility were inherited as nuclear recessives.Abbreviations f fertile - ps partially male sterile - s male sterile plants  相似文献   

5.
Digenic nature of male sterility in pepper (Capsicum annuum L.)   总被引:1,自引:0,他引:1  
Summary A cross was made between two nearly isogenic lines differing for male sterility genes, viz. ms1ms1Ms2Ms2 s Ms1Ms1Ms2ms2. F1 plants yielded F2 populations which segregated either in 3:1 or 9:7 ratios of fertile vs male sterile individuals. Test crosses between male sterile and male fertile sibs in the 9:7 segregating populations provided a few lines in which most of the progenies were male sterile. A 3:1 ratio model of male steriles vs fertiles is suggested and the value of the system is discussed.Contribution A.R.O. Agricultural Research Organization, The Volcani Center, Bet Dagan 50 250, Israel No. 3703-E, 1992 series.  相似文献   

6.
Brassicaceae crops display strong hybrid vigor, and have long been subject to F1 hybrid breeding. Because the most reliable system of F1 seed production is based on cytoplasmic male sterility (CMS), various types of CMS have been developed and adopted in practice to breed Brassicaceae oil seed and vegetable crops. CMS is a maternally inherited trait encoded in the mitochondrial genome, and the male sterile phenotype arises as a result of interaction of a mitochondrial CMS gene and a nuclear fertility restoring (Rf) gene. Therefore, CMS has been intensively investigated for gaining basic insights into molecular aspects of nuclear-mitochondrial genome interactions and for practical applications in plant breeding. Several CMS genes have been identified by molecular genetic studies, including Ogura CMS from Japanese radish, which is the most extensively studied and most widely used. In this review, we discuss Ogura CMS, and other CMS systems, and the causal mitochondrial genes for CMS. Studies on nuclear Rf genes and the cytoplasmic effects of alien cytoplasm on general crop performance are also reviewed. Finally, some of the unresolved questions about CMS are highlighted.  相似文献   

7.
J. H. Oard  J. Hu  J. N. Rutger 《Euphytica》1991,55(2):179-186
Summary Twenty-six male sterile plants grown in the field were recovered in the M7 generation from ethyl methane sulfonate-treated material of the rice cultivar M-201. Fertility increased five-fold when ratooned plants from the field were grown in a growth chamber with a 12 hour daylength. Crosses between mutant and normal fertile cultivars produced fertile F1 plants. Female fertility was normal as judged by percent seed set from unbagged panicles of parental and recombinant lines. Transgressive segregation for fertility was observed for all crosses in the F2 and F3 generations. Five of 37 F3 male sterile plants showed moderate levels of seed fertility under winter greenhouse conditions and reduced seed set when transplanted to summer field plots. Fertility data from reciprocal crosses suggested cytoplasmic factors had little or no effect on levels of male sterility in the mutant lines. Chi-squared analyses of F2 and F3 generation results indicated male sterility of the mutants is conditioned by two nuclear genes with epistatic effects.  相似文献   

8.
A germplasm collection of 152 diverse rapeseed accessions from Canada, China, France, India, Poland and South Korea was assayed for identifying new fertility restorers and sterility maintainers for a Tournefortii (tour) cytoplasmic male sterility (CMS) system in rape‐seed. Only 16 (10.5%) genotypes showed complete fertility restoration following hybridization with tour CMS line NE 409A. Notable among these were GSL 8851, GSL 8953, Mokpo # 9, Mali, Buk‐wuk‐13, Kuju‐27 and Mokpo # 84. As many as 78 (51.3%) genotypes were perfect maintainers of sterility, the remaining 58 (38.2%) genotypes were classified as partial maintainers. To study the inheritance of fertility restoration, 20 CMS (tour) rapeseed lines were crossed with the four best fertility restorers, namely GSL 8851, GSL 8953, Kuju‐27 and Mokpo # 9, to obtain F2 and test cross populations. Segregation data indicated that fertility restoration for tour CMS was governed by two genes, of which, one is stronger than the other (χ212:3:1). Differences in gene interactions were also observed (χ29:3:4) which could be explained on the basis of influence of female parent genotypes/or modified expression of the restorer gene(s) in different genetic backgrounds. Tests of allelism indicated that the restorer genes present in the four restorers evaluated were allelic.  相似文献   

9.
M. Nieuwhof 《Euphytica》1968,17(2):265-273
Summary The effect of temperature on the expression of male sterility was studied in clones of partially male sterile and completely male sterile plants of Brussels sprouts.At a low temperature (10°C) most clones of male sterile plants developed normal fertile flowers, but some clones showed an opposite reaction. The female fertility of the clones of the male sterile plants did not differ much from that of the fertile clones.These results point to a possibility of propagating male sterile lines of cole crops by selfing or sib-mating them at low or high temperatures.  相似文献   

10.
‘Ogura radish’, a cytoplasmic genetic male sterile line, was crossed with four local and three Japanese cultivars to identify maintainer lines. Out of seven F1 families, one cross involving a local cultivar, Aushi, produced 100% male sterile (MS) progeny. The crosses involving the other two local cultivars, Tangail Local and Kuni, produced about 90% MS progeny, indicating the presence of maintainer gene(s) for male sterility. The fourth local cultivar, Tasaki, produced 100% male fertile (MF) progeny. All three exotic cultivars appeared to possess the chromosomal gene(s) for controlling the male sterility. In BC1, BC2 and BC3 generations, segregation of MS plants were more frequent when ‘Aushi’ was used as recurrent parent. The expression of male sterility was not affected by seasonal influences. Thus the local cultivar ‘Aushi’ may be used as maintainer line for ‘Ogura radish’. To produce hybrid seed, ‘Tasaki’ can be used as pollinator line as it exhibit high heterosis with ‘Aushi’. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

11.
Summary Some plants without pods but with gynophores were observed in two F4 progenies of two crosses of goundnut (Arachis hypogaea L.). The flowers on these plants had translucent white anthers with no or a few sterile pollen grains. Three such plants in the succeeding generation were hand pollinated with pollen from a short-duration Indian cv. JL 24. The resulting F1 hybrid plants (male sterile x JL 24) were normal. Chi-square tests for segregation for male fertile and male sterile plants in F2 and F3 generations indicated that the male sterility in these crosses of groundnut is governed by two recessive genes. We designate these genes as ms1 and ms2 with ms1ms1ms2ms2 being a male sterile genotype.Submitted as ICRISAT J. A. No. 1812.  相似文献   

12.
Segregation studies following the transfer of the gene wi to different cytoplasm types, which have been distinguished by means of restriction fragment length polymorphism analyses using mitochondrial gene probes, revealed the formation of the wi‐sterility in each of the four cytoplasms examined. The male sterility is therefore only caused by the nuclear wi gene, i.e. an additional factor of a specific cytoplasm can be excluded. Hence, the wi‐sterility proved to be a genic male sterility (GMS) and not a cytoplasmic male sterility (CMS). The expression of the wi‐sterility appears to be stable, since it is not affected by high temperatures or tetracycline. Accordingly, a temporary pollen production, which would allow self‐fertilization for the maintenance of sterile lines, cannot be induced by controlling these environmental factors. In terms of hybrid breeding, this GMS therefore has no advantage over the previously described CMS system.  相似文献   

13.
Twenty‐three cytoplasmic male sterile BC1F1 barley lines were exposed to varying temperature treatments (TTs) to examine the effect of temperature on the stability of the expression of cytoplasmic male sterility (cms). The TTs used for this test were: (i) controlled low‐temperature treatment of 16°C (CL), (ii) controlled medium‐temperature treatment of 21–24/16–17°C day/night (CM) and (iii) ambient glasshouse‐temperature treatment of 24–41/16–17°C day/night (AG). The expression of cms was found to be variably influenced by temperature and by the genetic background of the cms recipient lines. Ten cms lines exhibited consistently complete male sterility over TTs, indicating that these lines are completely under cms genes control, while other lines showed partial revision to fertility across different TTs with profound influence of warm temperatures (CM and AG) in breaking down the cms in barley.  相似文献   

14.
Genetic male sterility (GMS) exists naturally in safflower (Carthamus tinctorius L.). In the existing safflower GMS lines, sterile and fertile plants are distinguishable at flowering. This causes delay in fertile plants rouging and reduction in hybrid purity. In this investigation, a cross between a spiny GMS parent 13‐137 and a spiny non‐GMS parent ‘A1’ was effected. One sib cross, SC‐67, producing non‐parental‐type non‐spiny sterile and spiny fertile plants in F3 was advanced to F9 through sib crossing between non‐spiny sterile and spiny fertile plants. Mendelian digenic segregation was not observed for non‐spiny trait and male sterility. The results revealed strong linkage between these traits. The linkage was confirmed in F2 generations of crosses between a non‐spiny marker‐linked GMS line (MGMS) and five elite lines. Male sterility–linked non‐spiny trait could distinguish sterile and fertile plants at elongation stage. The MGMS would be useful in production of pure F1 hybrid seed and development of elite populations.  相似文献   

15.
Summary Strong indication was found for the existence of a chromosal monogenic dominant male sterility-gene in chenese cabbage. This source of male sterility can be of practical use for the production of hybrid varieties. A pronounced drawback is the required removal, in the breeding and seed production stage, of the approximately 50% male fertile plants from each offspring of male sterile plants. Fortunately this removal is facilitated by the penomenon of apical dominace in the flowering process in the whole Brassica rapa taxon. Moreover an advantage of dominant monogenic male sterility is its easy and rapid introduction into all available genotypes of chinese cabbage.  相似文献   

16.
Summary To determine the origin of Ogura male sterile cytoplasm in radish (Raphanus sativus L.), wild and cultivated radishes were crossed. Three types of progeny resulted from the F1 hybrids between the wild radish from Kushikino with Ogura-type mtDNA and the cultivars (Uchiki-Gensuke or Comet). The segregation patterns of the male sterility were compared with those of Ogura cytoplasm. The male sterility induced in the F1 hybrid was maintained by crossing with Uchiki-Gensuke, that maintains Ogura male sterility. In the two types of progeny, in which Comet (a restorer of Ogura cytoplasm) was used as one of the parents, both fertile and sterile plants segregated at the predicted ratio on the assumption that a single dominant fertility restoring gene exists in the restorer. From these results, we concluded that the Ogura cytoplasm is identical to that of the wild radish, and the former originated in a population of Japanese wild radish.  相似文献   

17.
The study was aimed at the identification of random amplified polymorphic DNA markers linked to genes controlling male sterility in rye with the C‐source of sterility‐inducing cytoplasm. Markers of male sterility were distinguished using bulk segregant analysis, carried out on the two F2 crosses between male sterile and male fertile inbred lines. Screening of polymorphisms revealed by 1000 arbitrary 10‐mer primers allowed the detection of 10 markers in the cross between 711‐cmsC and DS2 lines and seven markers in the cross between 544‐cmsC and Ot0‐20 lines. Five markers were common for the two crosses, which allowed comparative mapping to be performed. Ten markers were mapped on the 4RL chromosome arm where two linked quantitative trait loci (QTL) for male sterility were discovered. Additional QTL of minor effect on male fertility were detected between the two linked markers provisionally assigned to the 6RS chromosome arm. The effectiveness of the marker‐assisted selection (MAS) for male‐sterile genotypes was evaluated.  相似文献   

18.
H. Ahokas 《Euphytica》1979,28(2):409-419
Summary 58 varieties, strains or mutants of barley were tested in the msml cytoplasm in Finland, location ca. 61 N. Three (5%) were found to be partial restorers, the rest being maintainers of sterility. 31 Israeli strains of wild barley (ssp. spontaneum) were tested. About one third were maintainers of sterility, the majority partial restorers, and two strains were full restorers. There is probably polymorphism of the restorer gene in Israeli wild barley. Partial restoration displays an environmental response. The physiology of partial restoration is discussed.  相似文献   

19.
The occurrence of genetic male sterility and development of highly sterile lines have been reported. The male sterility was not accompanied by any visible chromosomal aberration. It behaved as recessive and was governed by multiple factors. It was hypothesised that three major genes with additive effect were operating to produce highly sterile forms while less sterile forms would be dependent on one or two genes. The expression of male sterility was also influenced by modifying factors and environments.  相似文献   

20.
M. A. Hossain    M. A. K. Mian    M. G. Rasul 《Plant Breeding》2002,121(4):354-356
In a series of three experiments during 1998‐99 and 1999‐2000 at Gazipur, Bangladesh, the causes of segregation of Ogura cytoplasmic genetic male sterility in local cultivars of radish were studied. Male‐sterile populations at the BC5 and BC6 generations were grown under a range of field temperatures for 2 years and the results on pollen fertility tests revealed that the expression of male sterility was not affected by temperature. Neither was a genotype‐year interaction found. The unexpected segregation observed in the male‐sterile backcross generations might be due to the presence of restorer alleles in the maintainer parents.  相似文献   

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