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N o v e m b e r 2 6 - 2 7 , 2 0 1 8 | M a d r i d , S p a i n

Note:

Page 17

Euro Biotechnology 2018 & Genomics Congress 2018 & Cancer Congress 2018

Journal of RNA and Genomics

|

ISSN: 2591-7781

|

Volume 14

&

&

BIOTECHNOLOGY

Euro Congress on

GENOMICS AND MOLECULAR BIOLOGY

International Conference on

CANCER SCIENCE AND THERAPY

Global Congress on

Joint Event on

OF EXCELLENCE

IN INTERNATIONAL

MEETINGS

alliedacademies.com

YEARS

Kirankumar S Mysore, J RNA Genomics 2018, Volume 14

INSERTION MUTAGENESIS IN

MEDICAGO

TRUNCATULA

AND ITS UTILIZATION TO

IDENTIFY NOVEL SOURCES OF RESISTANCE

AGAINST ASIAN SOYBEAN RUST

R

etrotransposons, retrovirus like elements which encode proteins required

for their own replication and transposition can be used for insertional mu-

tagenesis. Tobacco retrotransposon,

Tnt1

, has been used to mutagenize and

tag the whole genome of a model legume

Medicago truncatula

.

Tnt1

is very ac-

tive and transpose into on average, 25 different locations during

M. truncatula

tissue culture. Mutations induced by

Tnt1

insertion are stable during seed to

seed generation. We have generated over 20,000 independent

Tnt1

-containing

lines encompassing more than 500,000 insertion events. Over 400,000

Tnt1

flanking sequence tags (FSTs) have been recovered and a database has been

established. We have pooled genomic DNA from all the lines for customized

reverse genetic screening and the frequency of insert identification in this pool

for average sized gene is approximately 85%. The range and diversity of mu-

tant phenotypes obtained to date suggest that

M. truncatula

offers a great

opportunity to dissect symbiotic and developmental pathways for compre-

hensive understanding of legume biology. A forward genetics approach using

Tnt1

tagged

M. truncatula

lines has been established (Fig. 1) to identify genes

that confer non host resistance to Asian Soybean Rust pathogen

Phakopso-

ra pachyrhizi

. Several

M. truncatula

Tnt1

mutants with altered response to

P.

pachyrhizi

have been identified and being characterized. irg1 (inhibitor of rust

germ-tube differentation1) mutant inhibited pre-infection structure differenti-

ation of

P. pachyrhizi

and several other bio-trophic pathogens. IRG1 encodes

a Cys (2) His (2) zinc finger transcription factor, PALM1 that also controls dis-

sected leaf morphology in

M. truncatula

. Characterization of other mutants

will also be presented.

Biography

Kirankumar S Mysore is a Professor at the Noble

Research Institute. He also holds Adjunct Profes-

sorship at the Department of Entomology and

Plant Pathology, Oklahoma State University. He

received his Bachelor’s Degree in Agriculture at the

University of Agricultural Sciences, Bangalore, In-

dia. He did Master’s Degree in Horticulture at Clem-

son University and PhD in genetics at Purdue Uni-

versity in 1999. He did his Postdoctoral training at

the Boyce Thompson Institute for Plant Research,

Cornell University. His main research interests

center on molecular plant-microbe interactions.

Research approaches in his group include genet-

ics and genomics to better understand how plants

defend against pathogens. He has published over

180 papers and book chapters in international jour-

nals.

ksmysore@noble.org

Kirankumar S Mysore

Noble Research Institute, USA