Marker assisted mobilization of cry1Ac gene from transgenic chickpea into cultivated chickpea (Cicer arietinum L.) for pod borer [Helicoverpa armigera (Hübner)] resistance

dc.contributor.advisorAjinder Kaur
dc.contributor.authorSharma, Urvashi
dc.date.accessioned2019-09-12T06:52:03Z
dc.date.available2019-09-12T06:52:03Z
dc.date.issued2019
dc.description.abstractHelicoverpa armigera (Hübner) poses a serious threat to chickpea production world-wide. cry1Ac gene is known to be most effective in controlling infestation of pod borer. The present investigation was undertaken to incorporate cry1Ac gene from T5 transgenic chickpea lines BS 100B-T5 and BS 100E-T5 into cultivated chickpea (Cicer arietinum L.) varieties PBG 7 and L 552, respectively through crossing and recurrent backcrossing. The BC1F1 progenies [F1 (PBG 7 x BS 100B-T5) x PBG 7] and [F1 (L 552 x BS 100E-T5) x L 552] were tested for cry1Ac gene presence using gene specific primers. ELISA on the positive plants revealed Cry1Ac protein content between 10.57 to 11.72 µg/g leaf tissue. Therefore, on the basis of foreground selection and ELISA, positive BC1F1 plants were propagated to obtain BC1F2 populations, which were also subjected to foreground selection. A BC2F2 population of 83 plants was also grown by selfing [F1 (PBG 7 x BS 100E-T5) x PBG 7] x PBG 7. Foreground selection using cry1Ac specific primers on BC2F2 population resulted in ten (12.04 %) cry1Ac positive plants (1, 2, 8, 9, 12, 20, 26, 33, 39 and 44); their background selection using 12 polymorphic SSR markers revealed average recurrent parent genome restoration of 88.9 %. As a result, BC2F3 population comprising 128 plants was obtained from ten cry1Ac positive BC2F2 plants. Each BC2F3 row of positive plants was then tested using cry1Ac specific primers to identify BC2F2 plants homozygous for cry1Ac gene. The analysis revealed that three (30 %) BC2F2 plants 26, 39 and 44 were homozygous for cry1Ac gene, whereas remaining seven plants 1, 2, 8, 9, 12, 20 and 33 segregated in ratios of 6:1, 2.3:1, 1.25:1, 3:1, 1.6:1, 4:1 and 3:1, respectively.en_US
dc.identifier.urihttp://krishikosh.egranth.ac.in/handle/1/5810127488
dc.keywordsPod borer, Foreground selection, Background selection, cry1Ac gene, ELISA, BC1F1, BC2F2 population and Homozygousen_US
dc.language.isoenen_US
dc.pages61en_US
dc.publisherPunjab Agricultural University, Ludhianaen_US
dc.research.problemMarker assisted mobilization of cry1Ac gene from transgenic chickpea into cultivated chickpea (Cicer arietinum L.) for pod borer [Helicoverpa armigera (Hübner)] resistanceen_US
dc.subAgricultural Biotechnologyen_US
dc.subjectnullen_US
dc.themeMarker assisted mobilization of cry1Ac gene from transgenic chickpea into cultivated chickpea (Cicer arietinum L.) for pod borer [Helicoverpa armigera (Hübner)] resistanceen_US
dc.these.typeM.Scen_US
dc.titleMarker assisted mobilization of cry1Ac gene from transgenic chickpea into cultivated chickpea (Cicer arietinum L.) for pod borer [Helicoverpa armigera (Hübner)] resistanceen_US
dc.typeThesisen_US
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