ISSR and SCAR markers linked to the mungbean yellow mosaic virus (MYMV) resistance gene in blackgram [Vigna mungo (L.) Hepper]

A recombinant inbred line (RIL) mapping population (F₈) was generated by crossing Vigna mungo (cv. TU 94‐2) with Vigna mungo var. silvestris and screened for mungbean yellow mosaic virus (MYMV) resistance. The inter simple sequence repeat (ISSR) marker technique was employed to identify markers linked to the MYMV resistance gene. Of the 100 primers screened, 54 showed amplification of which 36 exhibited polymorphism between the parents TU 94‐2 (resistant) and V. mungo var. silvestris (susceptible). Individual plants from 53 RIL populations were analysed and one marker (ISSR811₁₃₅₇) was identified as tightly linked to the MYMV resistant gene at 6.8 cM. Both the phenotype as well as the ISSR811₁₃₅₇ marker segregated in a 1 : 1 ratio. The ISSR811₁₃₅₇ marker was sequenced and sequence characterized amplified region (SCAR) primers were designed (YMV1‐F and YMV1‐R) to amplify the marker. Screening for the SCAR marker in the RIL population distinguished the MYMV resistant and susceptible plants, agreeing well with the phenotypic data. The ISSR811₁₃₅₇ marker was validated using diverse blackgram genotypes differing in their MYMV reaction. The marker will be useful for the development of MYMV‐resistant genotypes in blackgram.     

Inheritance of Cercospora Leaf Spot Resistance in Mung Bean, Vigna radiata (L.) Wilczek

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.     

Inheritance of seed resistance to bruchids in cultivated mungbean (Vigna radiata, L. Wilczek)

Bruchid beetles or seed weevils are the most devastating stored pests of grain legumes causing considerable loss to mungbean (Vigna radiata (L.) Wilczek). Breeding for bruchid resistance is a major goal in mungbean improvement. Few sources of resistance in cultivated genepool were identified and characterized, however, there has been no study on the genetic control of the resistance. In this study, we investigated the inheritance of seed resistance to Callosobruchus chinensis (L.) and C. maculatus (F.) in two landrace mungbean accessions, V2709BG and V2802BG. The F₁, F₂ and BC generations were developed from crosses between the resistant and susceptible accessions and evaluated for resistance to the insects. It was found that resistance to bruchids in seeds is controlled by maternal plant genotype. All F₁ plants derived from both direct and reciprocal crosses exhibited resistance to the bruchids. Segregation pattern of reaction to the beetles in the F₂ and backcross populations showed that the resistance is controlled by a major gene, with resistance is dominant at varying degrees of expressivity. Although the presence of modifiers was also observed. The gene is likely the same locus in both V2709BG and V2802BG. The resistant gene is considered very useful in breeding for seed resistance to bruchids in mungbean.     

Development of an interspecific Vigna linkage map between Vigna umbellata (Thunb.) Ohwi & Ohashi and V. nakashimae (Ohwi) Ohwi & Ohashi and its use in analysis of bruchid resistance and comparative genomics

To facilitate transfer of bruchid resistance to azuki bean (Vigna angularis) from its relatives an interspecific mapping population was made between rice bean, V. umbellata, and the related wild species V. nakashimae. The V. umbellata parent is completely resistant and V. nakashimae is completely susceptible to the bruchid beetle pests, azuki bean weevil (Callosobruchus chinensis) and cowpea weevil (C. maculatus). There is very low cross compatibility between V. umbellata and azuki bean. Therefore, V. nakashimae, that crosses with both V. umbellata and V. angularis without the need for embryo rescue, is used as a bridging species. A genetic linkage map was constructed based on an interspecific F₂ mapping population between V. umbellata and V. nakashimae consisting of 74 plants. A total of 175 DNA marker loci (74 RFLPs and 101 SSRs) were mapped on to 11 linkage groups spanning a total length of 652 cM. Segregation distortion was observed but only three markers were not linked to any linkage group due to severe segregation distortion. This interspecific genome map was compared with the genome map of azuki bean. Of 121 common markers on the two maps, 114 (94.2%) were located on the same linkage groups in both maps. The marker order was highly conserved between the two genome maps. Fifty F₂ plants that produced sufficient seeds were used for quantitative trait locus (QTL) analysis and locating gene(s) for C. chinensis and C. maculatus resistance in V. umbellata. The resistance reaction of these F₂ plants differed between C. chinensis and C. maculatus. Both resistances were quantitatively inherited with no F₂ plants completely susceptible to C. chinensis or C. maculatus. One putative QTL for resistance to each of these bruchid species was located on different linkage groups. Other putative QTLs associated with resistance to both C. chinensis and C. maculatus were localized on the same linkage group 1. Linked markers associated with the bruchid‐resistant QTL will facilitate their transfer to azuki bean breeding lines.     

Mapping a new source of resistance to powdery mildew in mungbean

Both restriction fragment length polymorphism (RFLP) and amplified fragment length polymorphism (AFLP) analyses were employed to map a new source of resistance to powdery mildew in mungbean. Disease scores of an F₂ population derived from the cross between a moderately resistant breeding line VC1210A and a susceptible wild relative (Vigna radiata var. sublobata, accession TC1966) showed a continuous distribution and was treated as a quantitative trait. Although no significant quantitative trait loci (QTL) that can explain the variation was detected by QTL analysis based on the reconstructed RFLP linkage map, new marker loci associated with resistance were discovered by AFLP analysis. The RFLP loci detected by two of the cloned AFLP bands are associated with resistance and constitute a new linkage group. A major resistance quantitative trait locus was found on this linkage group that accounted for 64.9% of the variation in resistance to powdery mildew. One of the probes developed in this study has the potential to assist in breeding for powdery mildew resistance in mungbean.     

Natural Outcrossing in Rice Bean

Natural outcrossing in rice bean (Vigna umbellata [Thumb.] Ohwi and Ohashi) was studied in the progenies of recessive plants in F generation of six crosses involving three loci — Ti (seed coat base colour), (seed coat mosaic) and Rr (seedling colour), The estimate of outcrossing (α) varied from 0.27 10 0.81 and the percentage of line showing outcrossing varied from 86.S to 100 and the outcrossing was non random.     

Interspecific hybridization between rice bean (Vigna umbellata) and its wild relative (V. minima): Fertility-sterility relationships

Summary The pre-and post-fertilization barriers in the interspecific crosses between Vigna umbellata and V. minima were investigated. In the reciprocal crosses (V. minima as the parent) the entry of pollen tubes into the ovary was delayed by about 4 h, and no seed set was observed. However, no pre-fertilization barriers were encountered in crosses involving V. minima as the parent and V. umbellata as the parent (normal cross). The delay/absence of divisions in the endosperm and the failure of embryo to divide were the post-fertilization barriers responsible for somatoplastic sterility in normal crosses which yielded a few hybrid seeds. The hybrid seeds showed poor germinability. The F₁ hybrids were intermediate between the parents in most morphological characters, and are completely sterile for pollen. Backcrossing of F₁ hybrid with both the parents did not restore fertility in the progenies. V. minima is considered as the tertiary gene pool of the rice bean.     

Partly fertile interspecific hybrid between a black gram × green gram derivative and an adzuki bean

A true‐breeding black gram (Vigna mungo) × green gram (Vigna radiata) derivative was reciprocally crossed with adzuki bean, Vigna angularis. Pollinated pistils were treated with gibberellic acid (GA₃) (70 p.p.m.) 24 and 48 h after pollination. One fertile pod containing two hybrid seeds was obtained, when V. angularis was used as the male parent. One of these seeds germinated and a partly fertile interspecific hybrid was obtained. Its hybridity was confirmed at the seedling stage based on the presence of the green epicotyl colour of the adzuki bean. Pubescence of epicotyl, stem, leaf margins and pod, and the colour of the mature pod, characteristics of the black gram × green gram derivative, were also expressed in the hybrid. In addition, the hybrid exhibited two novel traits — the presence of racemose inflorescence and plant regeneration ability — not present in the parents. The study of this hybrid and four offspring revealed that green epicotyl colour of adzuki bean, and the pubescence of stem and leaf margins of the black gram × green gram derivatives were dominantly inherited traits. Colours of epicotyl and stem bases were found to be linked.     

Interspecific hybridization between urdbean (Vigna mungo (L.) Hepper) and adzukibean (Vigna angularis (Willd.) Ohwi and Ohashi)

Summary To introduce resistance to fungal and viral diseases into urdbean (Vigna mungo), it was crossed with adzukibean (Vigna angularis) to achieve an interspecific hybrid between the two species by using different non-conventional breeding methods. Partial success was obtained with the use of UV irradiated pollen, intraspecific hybrids as parents and spray of immuno-suppressants on the female parent under glass house conditions and to the extent of callusing in aseptic culture.     

Estimation of additive, dominance and digenic epistatic interaction effects for certain yield characters in Vigna sesquipedalis Fruw

Inheritance of yield and yield contributing characters were investigated using generation mean analysis, utilising the means of six basic populations viz., P₁, P₂, F₁, F₂, BC₁P₁ and BC₁P₂ in four crosses of Vigna sesquipedalis. The analysis reiterated that the importance of dominance (h) gene effects for pod yield/plant and pods/plant as compared to additive (d) gene effects. However, significant and positive additive effects were noticed for pod yield/plant, pods/plant, pod weight and seed weight in different crosses. The three types of gene interactions (additive, dominance and epistasis) were significantly involved for pods/plant in cross KU 7 ×KU 8. Among the digenic epistatic interactions, both additive ×additive (i) and dominance × dominance (l) contributed more for pod yield/plant and pods/plant, however, it varied among the crosses. Populations having earliness can be developed as indicated by reducing dominance effects. Pedigree selection and heterosis breeding is suggested to exploit the fixable and non fixable components of variation respectively in Vigna sesquipedalis. This revised version was published online in July 2006 with corrections to the Cover Date.     

Resistance to cowpea mottle carmovirus in Vigna vexillata

Cowpea mottle carmovirus (CPMoV) causes grain yield losses of up to 75% in cowpea (Vigna unguiculata [L.] Walp.). There is no resistance to this virus among cultivated cowpea lines, but a high level of resistance exists in Vigna vexillata, a wild Vigna species. Fifty‐four accessions of V. vexillata germplasm collection at IITA were tested for resistance to CPMoV. Seedlings were mechanically inoculated with the virus and susceptibility or resistance was assessed by visual scoring of disease symptoms and serological analysis using antigen‐coated plate enzyme‐linked immunosorbent assay (ACP‐ELISA). All but three V. vexillata lines belonging to the variety angustifolia were resistant to CPMoV. Crosses were made between two resistant V. vexillata lines and the three susceptible lines. Segregation patterns observed in the F₂ and the backcross populations of all the crosses showed that resistance to CPMoV in V. vexillata is controlled by a single dominant gene, and the level of resistance conferred by this gene in V. vexillata is very high.     

Inheritance of flower and pod colour in cowpea (Vigna unguiculata L. Walp.)

Inheritance of flower colour and pod colour in cowpea (Vigna unguiculata L. Walp.) has followed a qualitative pattern. Purple flower colour is dominant over white flower colour, whereas black pod colour is partially dominant over white pod colour. A segregation ratio of 3 purple:1 white flowers in F₂ generations of two crosses indicated that white flower colour is controlled by a single recessive. Segregation ratio of F₂ 1 white:2 light black:1 black indicated that black pod colour is partially dominant over white pod colour and is governed by one gene. These results were further confirmed by backcross generations. White flower and pod colour are controlled by single recessive genes on separate chromosome. Gene symbols were assigned. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance and molecular tagging of MYMIV resistance gene in blackgram (Vigna mungo L. Hepper)

Yellow Mosaic disease (YMD) is one of the most destructive diseases of blackgram (Vigna mungo) causing heavy yield losses every year. Mungbean Yellow Mosaic India Virus (MYMIV) is one of the YMD causing begomoviruses prevalent in the major blackgram growing area (northern and central part) of India. Inheritance of MYMIV resistance gene was studied in blackgram using F₁, F₂ and F_2:3 derived from cross DPU 88-31(resistant)× AKU 9904 (susceptible). The results of genetic analysis showed that a single dominant gene controls the MYMIV resistance in blackgram genotype DPU 88-31. The F₂ population from the same cross was also used to tag and map the MYMIV resistance gene using SSR markers. Out of 361 markers, 31 were found polymorphic between the parents. However, marker CEDG 180 was found to be linked with resistance gene following the bulked segregant analysis. This marker was mapped in the F₂ mapping population of 168 individuals at a map distance of 12.9 cm. The validation of this marker in nine resistant and seven susceptible genotypes has suggested its use in marker assisted breeding for developing MYMIV resistant genotypes in blackgram.     

Transfer of powdery mildew resistance from Brassica carinata to Brassica oleracea through embryo rescue

Interspecific hybrid plants and backcross 1 (BC₁) progeny were produced through sexual crosses and embryo rescue between Brassica carinata accession PI 360883 and B. oleracea cvs Titleist’and‘Cecile’to transfer resistance to powdery mildew to B. oleracea. Four interspecific hybrids were obtained through application of embryo rescue from crosses with B. carinata as the maternal parent, and their interspecific nature confirmed through plant morphology and random amplified polymorphic DNA (RAPD) analysis. Twenty‐one BC₁ plants were obtained through sexual crosses and embryo rescue although embryo rescue was not necessary to produce first backcross generation plants between interspecific hybrids and B. oleracea. All interspecific hybrids and eight of the BC₁ plants were resistant to powdery mildew.     

Identification by genetic analysis of two races of Erysiphe polygoni DC. causing powdery mildew disease in mungbean

Powdery mildew disease is one of the important foliar diseases of mungbean. Earlier, resistance sources have been identified and their genetic nature studied, but there is no information on race identification of Erysiphe polygoni so far. Different genotypes having combinations of the host resistance genes Pm₁Pm₁Pm₂Pm₂‘TARM‐1’, Pm₁Pm₁pm₂pm₂ (S‐158‐16) and pm₁pm₁Pm₂Pm₂ (S‐2‐4‐1) and no resistance genes pm₁pm₁pm₂pm₂ (TPM‐1) were used in the present investigation. The genotypes were screened with four isolates from Akola, Trombay, Jabalpur and Gauribidanur centres in India. The interactions of resistant differentials with the Akola isolate were different from the other three isolates. The inheritance patterns of different resistance genes in various crosses also differed with respect to the Akola isolate. The variation observed in the Akola isolate could be explained as the result of mutation of the dominant avirulence Avr₁Avr₁ genes to virulence avr₁avr₁ genes corresponding to host resistance Pm₁Pm₁genes. Therefore, the Akola isolate is identified as a second race of E. polygoni.     

绿豆基因组SSR引物在豇豆属作物中的通用性

分子标记的种间通用性可降低其开发成本,提高利用效率,也有助于促进遗传研究较薄弱物种的分子遗传学研究。本文选取绿豆、小豆、豇豆及饭豆材料各3份, 分析1 205对新开发的绿豆基因组SSR引物在这些材料中的扩增效果,结果显示绿豆基因组SSR引物在豇豆、小豆和饭豆中的通用性比率分别为50.0%、73.3%和81.6%;多态性比率分别为4.1%、1.7%和1.5%;在4个种间均通用的引物469对。这些通用性SSR引物将有助于这4种食用豆类在多样性评价、连锁图谱的构建、基因定位及比较基因组学等方面的研究。     

Inheritance of tomato leaf curl virus resistance in Lycopersicon hirsutum f. glabratum

Summary Inheritance of resistance to tomato leaf curl virus (TLCV) was studied in the progenies derived from interspecific crosses between TLCV resistant Lycopersicon hirsutum f. glabratum line B 6013 and five susceptible cultivars (HS 101, HS 102, HS 110, Pusa Ruby and Punjab Chhuhara) of L. esculentum. P₁, P₂, F₁, F₂, B₁ and B₂ progenies of the five crosses were artificially inoculated with local strains of TLCV by means of the vector whitefly, Bemisia tabaci (Genn.). and the disease reaction was studied in all the crosses. Reaction of parents, F₁, F₂ and backcrosses suggests that resistance derived from L. hirsutum f. glabratum B 6013 is based on two epistatic genes, one from the wild parent and one from the cultivated one, resulting in a 13:3 segragation in the F₂.     

Inheritance of photoperiod response in mungbean (Vigna radiata [L.] Wilczek)

Summary A dominant or partially dominant gene for sensitivity to photoperiod in mungbean strain PI 180311 was identified and labeled Ps. The gene was expressed when strain P1180311, or crosses involving PI 180311 were grown in 16- or 14-hour photoperiods but was not expressed when the populations were grown in a 12-hour photoperiod or in the field at Columbia, Missouri. Dominance × dominance epistatic effects were indicated as governing days to flower in absence of the obvious effect of the Ps gene. A gene A for purple hypocotyl was independent of the gene Ps.Contribution No. 7894 from the Missouri Agriculture Experiment Station.     

Inheritance of resistance to Didymella lycopersici Klebb. in tomato (Lycopersicon Mill.)

Summary The inheritance of the resistance to Didymella lycopersici was studied on F₃- and Bc₁-lines from interspecific crosses of L. esculentum with L. hirsutum and with L. hirsutum glabratum. The resistance is not monogenic and is inherited in dominant fashion. The high h² values based on line means offer possibilities to seleet efficiently for enhanced levels of resistance.     

No evidence of apomixis in matroclinal progeny from experimental crosses in the genus <Emphasis Type="Italic">Fragaria</Emphasis> (strawberry) based on RAPDs

Crossing experiments in Fragaria have frequently resulted in some matroclinal progeny. These have been attributed to either accidental selfing and/or pollen contamination, or apomixis. In this study 202 carefully controlled intra and interspecific crosses in Fragaria were made. No progeny were produced from 164 interploid crosses made between diploids, hexaploids and octoploids but 38 intraploid crosses resulted in 904 F₁ plants, of which 42 (4.6%) were found to be morphologically matroclinal. All matroclinal progeny subsequently studied by RAPDs were found to be hybrids and not apomicts. The absence of apomixis among matroclinal progeny in this study casts doubt on previous reports of apomixis in Fragaria. Our results showed that the complete morphological similarity of progeny to the seed parent, even in recessive characteristics, cannot therefore be taken as evidence of apomixis, and may rather indicate the heterozygosity of the pollen parent, emphasising the need to use DNA markers for confirmation of apomixis.