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1.
Information on inheritance of isozymes and linkage maps in Trifolium pratense L is limited. Genetic analysis of 18 isozyme systems and three morphological traits (white vs. pink flower, present vs. absent leaf marker and green vs. sun-red stem) was conducted. Six loci of four isozymes had simple Mendelian inheritance. Joint segregation analyses among 8 isozyme loci and 3 morphological gene markers (55 pair-wise combinations) resulted in the assignment of one linkage group. Two morphological markers coding for flower (c) and stem (gs) color were found to be in the same linkage group based on the analyses of two segregating families. The recombination values of the two progenies for c-gs were 0.079 and 0.113. No linkage was found between any of the isozyme loci and the morphological traits. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

2.
H. Wagner  G. Wricke 《Plant Breeding》1991,107(2):124-130
Genetic markers are most useful in plant breeding but so far only a few morphological and isozyme markers are known in Beta vulgaris. In this paper, the isozyme systems aconitase (AGO), NADH-:dihydrolipoamiddehydrogenase (DIA), esterase (EST), fructose-1,6-bisphosphatase (FDP), and hexokinase (HK) were genetically analysed. Isoelectric focussing (IEF), vertical polyacrylamide gel electrophoresis (PAGE) and starch gel electrophoresis (SGE) were used to separate the isozymes. A total of eight loci could be identified. The allelic forms of Aco-1, Dia-1, Est-1, Est-5 and Hk-1 are active monomers. The gene products of Est-3 and Fdp-2 are active as dimers. Est-2 also showed allelic forms without activity; null-alleles.  相似文献   

3.
Summary A linkage map for watermelon (Citrullus lanatus) was constructed on the basis of RADP, ribosomal DNA restriction fragment length polymorphism (RFLP), isozyme, and morphological markers using F1BC1. A segregating population of 78 individuals was the result of a backcross of a cultivated inbred line (H-7; Citrullus lanatus; 2n=22) and a wild form (SA-1; C. lanatus; 2n=22), in which the latter was the recurrent (male) parent. A total of 69 RAPD, one RFLP, one isozyme, and three morphological markers was found to segregate in the BC1 population. Linkage analysis revealed that 62 loci could be mapped to 11 linkage groups that extended more than 524 centimorgans (cM), while 12 loci segregated independently of all other markers. The locus for exocarp color was linked to two RAPD markers within a region of 5 cM on linkage group 4. The locus for flesh color was linked to a RAPD marker within a region of 30 cM on linkage group 6. The isozyme marker GOT was located on the linkage group 1. Linkage group 2 contained a locus for ribosomal DNA within 5 cM of a RAPD marker. Half of the RAPD markers on the linkage group 7 displayed severely distorted segregation. The construction of linkage map using molecular markers is necessary for the breeding of watermelon to introduce useful gene of wild watermelon efficiently. However the linkage map that was constructed for the most part on the basis of RAPD markers could not cover significant parts of the genome, the linkage map provides breeders of watermelons the possibility of tagging useful agronomic traits, as well as the gene for exocarp color.Abbreviations RAPD random amplified polymorphic DNA - RFLP restriction fragment length polymorphism - GOT glutamate oxaloacetate transaminase - MDH malate dehydrogenase - ACP acid phosphatase - 6PGH 6-phosphogluconate dehydrogenase  相似文献   

4.
Summary An analysis of linkage in sugarbeet (Beta vulgaris L.) was conducted for nine isozyme loci, Ak 1, Gdh 2, Idh 1, Lap, Mdh 1, Mdh 3, Pgi 2, Pgm 1,and Skdh 2,and four marker loci, annuality (B), red hypocotyl-color (R), pollen fertility restorer (X), and monogermity (m). Four linkage groups were identified; R-B-Idh 1, Gdh 2-Mdh 1, Ak 1 -Lap, and Mdh 3-Pgm 1.In addition, X was linked to Mdh 1and Skdh 2with a recombination value of 13.4% and 34.7%, respectively, and m was linked to Pgm 1with a recombination value of 35.8%. Pgi 2was inherited independently of the four linkage groups. This locus showed a skewed ratio in F2 progeny of a cross between self-compatible and self-incompatible lines and the allele derived from self-incompatible parents decreased markedly. On the other hand, the expected segregation ratio was observed in the backcrossed progeny and also in F2 progeny of a cross between self-compatible lines. The results obtained suggest that Pgi 2may be linked to a self-compatibility locus (S f)and the two loci may be assigned to an additional linkage group.  相似文献   

5.
Summary Polymorphism at isozyme loci was used to locate factors responsible for variation in quantitative traits of lentil. Eight sets of random single seed descent (RSSD) derived lines were developed by advancing individual F3 plants of interspecific (L. culinaris Medik. × L. orientalis Boiss.) hybrids to the F6. The RSSD lines in each of the eight sets differed for alleles at 2–8 isozyme loci. In each set, association of isozyme loci with variation in seven quantitative traits (days to flower, days to mature, plant height, biomass, seed yield, harvest index, seed weight) was determined for each pairwise combination of a quantitative trait with a marker locus. Loci affecting variation in all seven quantitative traits were detected by their association with 14 isozyme markers (Aat-c, Aat-m, Aat-p, Adh-1, Fk, Gal-1, Gal-2, Lap-1, Lap-2, Pgd-p, Pgi, Pgm-c, Pgm-p, Skdh). The known position of 10 the 14 isozyme loci on the lentil genetic map was used to mark the genomic regions for possible location of associated quantitative trait loci (QTL). Detected QTL were found to be located in six of the seven linkage groups on lentil genetic map. Regions of the genome represented by linkage groups, 1, 5 and 7 appeared to affect a greater number of traits than other genomic regions represented by linkage groups 2, 3 and 4. Results indicated that the mean expression of quantitative traits at segregating marker locus classes can be used to locate the genetic factors in lentil which influence the behavior of economically important traits.  相似文献   

6.
Summary Wide compatible varieties (WCVs) show normal spikelet fertility in crosses with Indica and Japonica rice varieties. Crosses of Indica and Japonica varieties frequently show high spikelet sterility which prevents exploitation of heterosis for grain yield. We screened 41 rice varieties for the wide compatibility trait by crossing each with three Indica and three Japonica testers. Varieties giving fertile F1 hybrids with both groups of testers were classified as WCVs. Seven varieties viz., BPI-76 (Indica); N 22; Lambayeque-1 and Dular (Aus); Moroberekan, Palawan and Fossa HV (Japonicas), were identified as WCVs. The frequency of WCVs was higher among Aus and Japonicas. The wide compatibility trait in varieties: Dular and Moroberekan was controlled by a single dominant gene linked with the Est-2 and Amp-3 loci (mean recombination 32.0%). Est-2 and Amp-3 showed complete linkage. Pgi-2 was found to be linked with Est-2 and Amp-3 (mean recombination 16.1%). Est-2 and Amp-3, showed a tighter linkage with C + (mean recombination 4.1%). Pgi-2 showed a lower linkage with C + (mean recombination 17.3%). The recombination values between the WC gene in Dular and C + was much higher than those reported in Japan for the WC gene (S5 n) from Ketan Nangka. It is possible that the WC gene from Dular is different from that in Ketan Nangka. Linkage intensities with the WC gene were not strong enough to be of use for indirect selection for the wide compatibility trait. A search for a more closely linked isozyme or DNA marker was proposed.  相似文献   

7.
L. Westphal  G. Wricke 《Euphytica》1991,56(3):259-267
Summary Electrophoretic polymorphisms of eight enzyme systems were studied in leaves of Daucus carota ssp. sativus in order to identify additional isozyme loci and generate first linkage groups of genetic markers. The genetic analysis of aconitase (ACO), leucin aminopeptidase (LAP), menadione reductase (MDR), phosphoglucomutase (PGM), 6-phosphogluconic dehydrogenase (6-PGD), shikimate dehydrogenase (SKD), and triose phosphate isomerase (TPI) zymograms resulted in the identification of 8 isozyme marker loci, designated as Aco-1, Lap-1, Pgm-1, Pgm-3, 6-Pgd-2, Skd-1, Tpi-1, and Tpi-2. All loci segregated with codominant alleles and encoded for monomers (ACO, LAP, PGM, SKD), and dimers (6-PGD, TPI), respectively. MDR enzymes of the variable region MDR-2 appeared to be identical with Dia-2 isozymes. Tests of joint segregation for pairwise comparisons of all 14 isozyme marker loci now available in carrots indicate that 12 loci are linked in 4 linkage groups (marked K1 to K4) in the following order: Aco-1, Pgi-1, and Dia-3 (K1), Tpi-2, Got-2, and Lap-1 (K2), Got-3 and Tpi-1 (K3) and Pgm-1, Pgm-3, 6-Pgd-2 and Skd-1 (K4). Dia-2 and Got-1 remained unlinked. The possible duplication of a PGM locus and a 6-PGD locus is discussed.  相似文献   

8.
Summary Genetic and linkage analysis of marker loci were performed with 4 selfed progenies, derived from single plant (I0/1 lines) of carrot (Daucus carota L. sativus). The analysis of 58 markers included 1 morphological marker, 10 isozyme loci, 14 RFLPs, 28 RAPD markers, and 6 isolated PCR fragments used as RFLP probes. Linkage analysis was carried out with the MAPMAKER program and resulted in the construction of 8 linkage groups containing 55 markers with an average distance of 13.1 cM, 3 marker loci remained unlinked. 24% of the markers deviated significantly from the expected Mendelian ratios (1:2:1 or 3:1) due to gametic or zygotic selection. It was shown that isolated PCR amplification products can be used as RFLP probes to detect polymorphisms for a certain locus in progenies where the corresponding RAPD pattern is monomorphic or no amplification product is observed. Since carrot has a relative small genome the probability of amplifying repetitive DNA sequences is comparatively low. Thus PCR amplification products represent an additional useful source of RFLP probes.  相似文献   

9.
Summary We report on the inheritance of 11 morphological markers and 17 isozymes in lentil (Lens culinaris). The monogenic inheritance of 11 morphological markers and 11 isozymes is confirmed. The inheritance of six isozymes (Aco-2, Enp, Est-3, Est-4, Lap-3, and Mdh-m) is reported for the first time in lentil. This brings the total number of described genes in lentil to 78. Cases of disturbed segregation were more frequent than expected by chance. It is suggested that disturbed segregation was in most cases caused by linkage with a piece of chromosome that showed preferential elimination in crosses between Lens culinaris ssp. odemensis and other subspecies. The prevalence of disturbed segregation in crosses with Lens culinaris ssp. odemensis could limit the usefulness of this subspecies in genetic and linkage studies.  相似文献   

10.
Summary Employing polyacrylamide gradient-gel electrophoresis, the genetic control of leaf glutamate oxaloacetate transaminase (GOT) isozyme variants and their linkage to ds1 (desynapsis), y (tuber flesh colour), cr (crumpled) and yc (yellow cotyledon) were studied in diploid tuberous Solanum species hybrids.Leaf GOT isozymes proved to be dimeric and under the control of two independently segregating loci (Got-1 and Got-2) with two (1 s , 1 f ) and three (2 s , 2 f , 2 n )alleles respectively. The 2 n allele was concluded to encode a 2 fallozyme subunit capable of forming heterodimeric but no homodimeric active molecules. As expected with Got-1 and Got-2 isozymes being localized in different cellular compartments, no intergenic heterodimer formation was observed.In contrast to earlier studies, a gradual rather than discrete transition between the tuber flesh colour classes white and yellow was observed in segregating progenies. Adopting a standardized classification method, however, monogenic recessive inheritance of white tuber flesh was confirmed. Got-1, ds1 and cr were found to represent a single linkage group. Among the presently studied marker loci no further linkages were detected. As to linkage analysis, the difficulties imposed by gametophytic incompatibility in nearly all diploid potato species and by the frequent occurrence of recessive (sub)lethal genes are discussed.  相似文献   

11.
Summary Isozyme variation and inheritance were investigated with starch gel electrophoresis in peach (Prunus persica L. Batsch) x P. kansuensis Rehd. and peach x P. davidiana (Carr.) Franch. interspecific hybrids. Of five enzyme systems surveyed for polymorphism, four systems were identified as polymorphic [isocitrate dehydrogenase (IDH, EC 1.1.1.41), phosphoglucomutase (PGM, EC 2.7.5.1), aspartate aminotransferase (AAT, EC 2.6.1.1), and 6 phosphogluconate dehydrogenase (PGD, EC 1.1.1.44)] and may be useful as genetic markers in future cultivar and rootstock development. Analysis of progenies segregating for pairs of loci suggests a possible linkage between the loci coding for Aat-1 and Pgd-2. Independent assortment was observed for isozyme loci Idh/Pgm-2, Idh/Aat-1, Idh/Pgd-2, Pgm-2/Aat-1, Pgm-2/Pgd-2, and Aat-2/Aat-1. The red leaf locus, Gr, assorted independently of the isozyme loci: Idh, Pgm-2, Aat-1, and Pgd-2.  相似文献   

12.
Marker-based selection of Ep-D1b has been used successfully to incorporate Pch1, the gene for eyespot resistance on chromosome 7D, into commercial wheat. However, attempts to transfer resistance conferred by Pch1 (on chromosome 7A) through selection for Ep-A1b have not always been successful. Linkage relations among eyespot resistance gene Pch2, a gene encoding for an isozyme of endopeptidase, Ep-A1b, and RFLP marker Xpsr121 on chromosome 7A were determined using 80 homozygous recombinant substitution lines. The recombinant lines were derived from eyespot susceptible ‘Chinese Spring’ hybridized with a resistant disomic substitution line of ‘Cappelle Desprez’ that has chromosome 7A substituted into ‘Chinese Spring’. Segregations of Pch2, Ep-A1b and Xpsr121 fit an expected 1:1 single-locus ratios based on χ2 tests. Linkage analysis revealed that Pch2 was not tightly linked to Ep-Alb (15% recombination). However, close linkage (3.8% recombination) existed between Ep-A1b and Xpsr121. The order of these loci is Pch2-Xpsr121-Ep-A1b. Unlike Pch1 and Ep-D1b, where little or no recombination is found, Pch1 and Ep-A1b showed considerable recombination and therefore linkage cannot be utilized efficiently in marker-based selection.  相似文献   

13.
Isozymes are useful biochemical markers in plant breeding. This paper presents the first results on the inheritance of three enzyme systems: diaphorase (DIA), glutamate oxalacetate transaminase (GOT) and phosphoglucoisomerase (PGI) from leaves of Daucus carota L. ssp. sativus and the linkage relationships among these isozyme loci, marked Dia, Got, and Pgi. Methods of extraction and electrophoresis are described. Segregation ratios indicated that the DIA system is controlled by three genes: Dia-1, Dia-2 and Dia-3, Dia-1 as invariant. Two codominant alleles and a null allele were found for Dia-2, and four codominant alleles for Dia-3-GOT isozymes are encoded by three genes; Got-1, Got-2 and Got-3. An active allele and a null allele were observed for Got-1, two codominant alleles for Got-2 and Got-3, respectively. PGI isozymes are controlled by a single gene, Pgi-1, with two codominant alleles. Altogether one invariant isozyme locus and six polymorphic loci are postulated. Test of joint segregation suggested a linkage of Dia-3 and Pgi-1. The recombination value is 0.04 ± 0.009.  相似文献   

14.
Summary Four newly detected accessions of wild barley (Hordeum vulgare ssp. spontaneum) resistant to powdery mildew caused by Blumeria graminis f. sp. hordei were studied with the aim of finding the number of genes/loci conferring the resistance of individual accessions, the type of inheritance of the genes and their relationships to the Mla locus. F2 populations after crosses between the winter variety ‘Tiffany’ and four wild barley accessions and use of microsatellite DNA markers were focused on the identification of individual resistance genes/loci by means of their chromosomal locations. In PI466495, one locus conferring powdery mildew resistance was identified in highly significant linkage with the marker Bmac0213. This location is consistent with the known locus Mla on chromosome 1HS. In the other three accessions the resistance was determined by two independent loci. In PI466197, PI466297 and PI466461, one locus was identified on chromosome 1HS and three new loci were revealed on chromosomes 2HS (highly significant linkage with Bmac0134), 7HS (highly significant linkage with Bmag0021) and 7HL (significant linkage with EBmac0755). Our prospective aim is identification of further linked DNA markers and the exact location of the resistance genes on the barley chromosomes.  相似文献   

15.
Hypersensitive, race specific genes primarily have been deployed to control powdery mildew (Blumeria graminis (DC) EO Speer f. sp. tritici) in wheat (Triticum aestivum L.); however, recent efforts have shifted to breeding for more durable resistance. Previously, three quantitative trait loci (QTL) for adult plant resistance (APR) to powdery mildew in the winter wheat cultivar Massey were identified in a Becker/Massey (BM) F 2:3 population. Fourteen new simple sequence repeat (SSR) markers were added to the pre-existing BM F 2:3 linkage maps near the QTL for APR on chromosomes 1BL (QPm.vt-1BL), 2AL (QPm.vt-2AL), and 2BL (QPm.vt-2BL). Genetic linkage maps comprised of 17 previously and newly mapped SSRs from the BM population on chromosomes 1BL, 2AL, and 2BL were constructed in a USG 3209/Jaypee (UJ) F 6:7 recombinant inbred line (RIL) confirmation population, wherein the APR resistance of USG 3209 was derived from Massey. Interval mapping analysis of mildew severity data collected in 2002 (F 5:6) and 2003 (F 6:7) field experiments with marker genotypic data obtained in 2003 (F 6:7) confirmed the presence of the three QTL governing APR to powdery mildew in the UJ RILs. The QTL QPm.vt-1BL, QPm.vt-2AL, and QPm.vt-2BL explained 12–13, 59–69, and 22–48% of the phenotypic variance for powdery mildew severity in the UJ confirmation populations, respectively, in two field experiments. The current study verified that the elite wheat cultivar USG 3209 possesses the same QTL for APR as its parent Massey.  相似文献   

16.
S. Y. Lin  H. Ikehashi 《Euphytica》1993,67(1-2):35-40
Summary A locus for male gamete abortion in hybrids for Japonica and Indica rice was identified with the aid of marker genes Rc and Est-9 on chromosome 7. In an Indica-Japonica cross, AKAMAI 1/IR50, the Indica allele Est-9 2 was transmitted via the male gamete with a ratio of 0.29 instead of the normal 0.5, whereas no segregation distortion was observed for the Rc locus. The recombination value (p) for Est-9 and Rc was estimated to be 0.38 by a least square method after adjusting Mendelian segregation ratios with the male transmission ratios of 0.29 (Tr) for Est-9 2 and 0.71 (1-Tr) for Est-9 1. The recombination value (q) for the new locus for male gamete abortion, ga-11, and Est-9 was estimated to be 0.23 by using 56 F3 lines from F2 plants which were heterozygous for the Est-9 locus. No linkage for Rc and ga-11 was found. Therefore, the two markers and ga-11 were located in the order of ga-11-Est-9-Rc. Using the estimated recombination value (q), the male transmission rate (k) of ga-11 a was estimated to be 0.11 with the F2 data and-0.07 with the F3 line data. Thus, it was apparent that male gametes possessing ga-11 a were frequently aborted in the Indica-Japonica hybrid.  相似文献   

17.
Summary Resistance to Plasmodiophora brassicae Wor. race 7, the causal agent of the disease clubroot, was examined in an F2 population of a cross between a clubroot resistant broccoli (Brassica oleracea var. italica) and a susceptible cauliflower (B. oleracea var. botrytis). A genetic linkage map was constructed in the same population based on the segregation of 58 dispersed restriction fragment length polymorphism (RFLP) markers. Associations between the inheritance of RFLP marker genotypes and segregation for disease resistance, morphological and maturity characteristics were examined. For each triat examined, several chromosomal regions marked by RFLP probes appeared to contain trait loci, suggesting that each trait was under polygenic control. RFLP marker linkage to a major factor imparting dominance for clubroot resistance from the broccoli parent was observed in this population. Additionally, RFLP marker linkage to an independently segregating factor contributing clubroot resistance from the cauliflower parent was observed, indicating that it should be possible to use RFLP markers to facilitate selection of transgressive segregants having the combined resistance from both parental sources. In some instances, RFLP markers from the same or closely linked chromosomal regions were associated with both clubroot resistance and morphological traits. Analysis of RFLP marker genotypes at linked loci should facilitate the selection of desired disease resistant morphotypes.  相似文献   

18.
Abstract: A partial linkage map of melon was constructed from a cross between PI414723 and Dulce. Twenty-two SSR, 46RAPD, 2 ISSR markers and four horticultural markers [female flower form (a), Fusarium resistance, striped epicarp (st), and fruit flesh pH (pH)] were analyzed in an F2/F3 population to produce a map spanning 14 linkage groups. We report for the first time map positions for the st, a, and pH genes. One SSR marker was tightly linked to pH. Mapping the a gene for the female flower form to molecular linkage group 4 enabled the merging of the map of horticultural traits with the of molecular markers in this region. Using the 22 SSR markers of this map, two of the three postulated ZYMV resistance genes were located using a BC1 population (PI414723 recurrent parent). One SSR marker was tightly linked to a ZYMV resistance gene, designated Zym-1. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

19.
Isoelectric focusing (IEF) and immunoblotting were used to detect genetic variants of malt endopeptidase (MEP1), an enzyme related to malting quality in barley and coded by the CepB locus on barley chromosome 3 (= 3H). A variant was found in a Turkish accession of wild barley (Hordeum vulgare ssp. spontaneum). The self progeny of a hybrid between this accession and the barley cultivar ‘Clipper’ were analyzed for recombination between the CepB locus and other isozyme loci. The estimates of recombination linked the CepB locus to an NADH diaphorase locus (Ndh2), which in turn was linked to the seedling esterase complex (Est1, Est2, and Est4) situated near the distal end of the long arm of chromosome 3. The Ndh2 locus was independent of two other NADH dehydrogenase loci (Ndh3, Ndh5) which were mapped on barley chromosome 5 (= 1H) in relation to the three hordein loci (Hor1, Hor2, and Hor3).  相似文献   

20.
The inheritance ot nine isozyme systems in selfed progenies of chives was studied elcctrophoretically. The isozyme systems studied were malate-dehydrogenase (MDH), phosphoglucoisomerase (PGI), triosephosphate-isomerase (TP1), diaphorase (D1A), menadione-reductase (MDR), esterase (EST), glutamate-oxalacetate-transaminase (GOT), hexokinase (HK) and superoxide-dismutase (SOD). Segregation results of Goodness-of-Fit tests against the expected 1:2:1 and 3 : 1 ratios for codominant and dominant inheritance, respectively, led to the identification of 16 isozyme loci whose banding patterns are given in this paper. The first results on linkage relationships between isozyme loci and between the Mdr-3-locus and a male sterility gene are given. These results and further studies will be used to mark important characters in chives.  相似文献   

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