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Identification of novel
mutations performed by
mapping by sequencing
led to the isolation of
agronomically interesting
mutant lines. (
 Moneymaker cultivar accession LA2706
 S. pimpinellifolium (accession LA1589) were used as a pollen
donor to obtain F2 interspecific populations.
 Three different EMS concentration were analyzed, i.e., 0.5%,
0.7%, and 1.0% by using 5 replicates of 100 seeds for each
treatment.
Overview
of
Mutagenesis
procedure
Total no of
16,104 MM
seeds were
EMS treated
12,560 M1 plants
were obtained,
from which 7379
(58.75%)
produced M2
segregating
progenies.
M2 progenis were
screened under
greenhouse
conditions along
eight crop cycles
to detect
recessive mutants
2800 mutants
(37.95%) were
detected and
grouped into 14
phenotypic
categories
EMS mutant lines displaying alterations during vegetative
and reproductive development
5
Gene isolation
of casual
mutation
 Scanning electron microscopy (SEM)
proved that sepals of mutant plants
lack the abscission zone between each
sepal.
 Therefore, they have called this
mutant sepal indehiscent (sin).
 Tomato mutants have been and
are still directly used in breeding
programs, but natural variation of
agronomically interesting alleles is
scarce in natural germplasm.
 Induced mutagenesis rises as one
of the most relevant genomics
tools to allow for the functional
characterization of most of the
unknown tomato genes.
 The identification of
novel mutations
performed by
mapping by
sequencing has led
to the isolation of
causal mutations of
agronomically
interesting mutant
lines.
 Such is the case of
the line UAL-7334
(sin), where this
approach has
allowed us to relate a
single nucleotide
deletion in the Auxin
Response Factor 10A
(SlARF10A) gene to
this mutant
phenotype.
 The use of another species
genetically distant from
cultivated tomato provides a
huge number of
polymorphisms for linkage
analysis, simplifying the
bioinformatic workflow, and
ensures a high mapping
accuracy.
Conclusion
Mutation in tomato using EMS and gene discovery.pptx

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Mutation in tomato using EMS and gene discovery.pptx

  • 1. Identification of novel mutations performed by mapping by sequencing led to the isolation of agronomically interesting mutant lines. (  Moneymaker cultivar accession LA2706  S. pimpinellifolium (accession LA1589) were used as a pollen donor to obtain F2 interspecific populations.  Three different EMS concentration were analyzed, i.e., 0.5%, 0.7%, and 1.0% by using 5 replicates of 100 seeds for each treatment.
  • 3. Total no of 16,104 MM seeds were EMS treated 12,560 M1 plants were obtained, from which 7379 (58.75%) produced M2 segregating progenies. M2 progenis were screened under greenhouse conditions along eight crop cycles to detect recessive mutants 2800 mutants (37.95%) were detected and grouped into 14 phenotypic categories
  • 4. EMS mutant lines displaying alterations during vegetative and reproductive development
  • 5. 5 Gene isolation of casual mutation  Scanning electron microscopy (SEM) proved that sepals of mutant plants lack the abscission zone between each sepal.  Therefore, they have called this mutant sepal indehiscent (sin).
  • 6.
  • 7.  Tomato mutants have been and are still directly used in breeding programs, but natural variation of agronomically interesting alleles is scarce in natural germplasm.  Induced mutagenesis rises as one of the most relevant genomics tools to allow for the functional characterization of most of the unknown tomato genes.  The identification of novel mutations performed by mapping by sequencing has led to the isolation of causal mutations of agronomically interesting mutant lines.  Such is the case of the line UAL-7334 (sin), where this approach has allowed us to relate a single nucleotide deletion in the Auxin Response Factor 10A (SlARF10A) gene to this mutant phenotype.  The use of another species genetically distant from cultivated tomato provides a huge number of polymorphisms for linkage analysis, simplifying the bioinformatic workflow, and ensures a high mapping accuracy. Conclusion

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