<mods:mods version="3.3" xsi:schemaLocation="http://www.loc.gov/mods/v3 http://www.loc.gov/standards/mods/v3/mods-3-3.xsd" xmlns:mods="http://www.loc.gov/mods/v3" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance"><mods:titleInfo><mods:title>Development of transgenics for fungal resistance and discovery of chemically induced mutations in Pearl Millet (Pennisetum glaucum L.) population by TILLING</mods:title></mods:titleInfo><mods:name type="personal"><mods:namePart type="given">N</mods:namePart><mods:namePart type="family">Jalaja</mods:namePart><mods:role><mods:roleTerm type="text">author</mods:roleTerm></mods:role></mods:name><mods:abstract>Protocols for in vitro plantlet regeneration in pearl millet and genetic transformation using inflorescence&#13;
derived callus cultures via Agrobacterium and microprojectile methods were standardized. Transgenic&#13;
pearl millet plants were confirmed by gene specific amplification of chitinase and osmotin and also the&#13;
bar genes. However, the transgenics turned out to be sterile, though pollen was produced.&#13;
� Mutagenized population of pearl millet from inbred line P1449-2-P1 was produced using the chemical&#13;
mutagen ethylmethane sulfonate and M2 generation was raised. Phenotypic analysis was carried out in&#13;
M2 generation. The mutagenized population was screened for point mutations using the TILLING&#13;
technique.&#13;
� The mutant lines (9,938 lines) were screened for two candidate genes, one associated with water stress&#13;
(dehydration responsive element binding factor, DREB2A) and the second associated with pathogen&#13;
resistance (enhanced disease resistance, EDR2).&#13;
� Allele mining was carried out for DREB2A gene; amino acid arginine was changed to threonine and&#13;
serine to proline in the hot spot region that was predicted by the CODDLE software. It is hoped that these&#13;
amino acid changes would bring loss of function of this gene and thus can help to find out the function of&#13;
the gene under water stress conditions.&#13;
� TILLING was performed for EDR2 gene; but because of non-specificity, the mutations could not be&#13;
detected in the LICOR gel.</mods:abstract><mods:classification authority="lcc">Millets</mods:classification><mods:originInfo><mods:dateIssued encoding="iso8061">2011</mods:dateIssued></mods:originInfo><mods:originInfo><mods:publisher>Osmania University;Department of Genetics</mods:publisher></mods:originInfo><mods:genre>Thesis</mods:genre></mods:mods>