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Molecular Markers in Crop Improvement

Indian Institute of Pulses ResearchKanpur - 208 024 Easy & rapidReproducible genotypingAccurate phenotypingAuthentic mapping populationChoice of parentsMolecular Markers in Crop ImprovementMolecular Markers in Crop ImprovementAgr search with a uman touchAgr search with a uman touchgj dne] gj Mxjfdlkuksa dk gelQjHkkjrh; d`f"k vuqla/kku ifj"knICARHkkd`vuqiHkknvlF POU LESTEUSTI RTESSNIE ANRAICDHNIM olecular Markers inCrop ImprovementD. DattaSanjeev ChaturvediN. NadarajanIndian Institute of Pulses ResearchKanpur - 208 024 ICARP rinted:September, 2011 Published by:Dr. N. Nadarajan, DirectorIndian Institute of Pulses Research, KanpurEdited by:Mr.

principles as phenotypic alleles. Mostly, molecular alleles are selectively neutral. Theories of population genetics apply to molecular alleles as well. Backcross It is the cross of an F 1 hybrid to any one of the homozygous parents. Testcross It is the cross of any individual to a homozygous recessive parent. It is used to determine if

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Transcription of Molecular Markers in Crop Improvement

1 Indian Institute of Pulses ResearchKanpur - 208 024 Easy & rapidReproducible genotypingAccurate phenotypingAuthentic mapping populationChoice of parentsMolecular Markers in Crop ImprovementMolecular Markers in Crop ImprovementAgr search with a uman touchAgr search with a uman touchgj dne] gj Mxjfdlkuksa dk gelQjHkkjrh; d`f"k vuqla/kku ifj"knICARHkkd`vuqiHkknvlF POU LESTEUSTI RTESSNIE ANRAICDHNIM olecular Markers inCrop ImprovementD. DattaSanjeev ChaturvediN. NadarajanIndian Institute of Pulses ResearchKanpur - 208 024 ICARP rinted:September, 2011 Published by:Dr. N. Nadarajan, DirectorIndian Institute of Pulses Research, KanpurEdited by:Mr.

2 Diwakar UpadhyayaPrinted by : Army Printing Press, 33, Nehru Road, Sadar Cantt, Lucknow Tel: 0522-2481164 Correct citation:Datta, D., Gupta, Sanjeev, Chaturvedi, and Nadarajan, N. (2011): Molecular Markers in Crop Improvement . Indian Institute of Pulses Research,Kanpur - 208 024 PrefaceWith the advent of marker -assisted selection (MAS), a new breedingtool is available to make more accurate and useful selections in breedingpopulations. MAS allows heritable traits to be linked to the DNA segments thatare responsible for controlling that trait. These segments of DNA or QTLs(Quantitative Trait Loci) can be detected through specific laboratory most commonly used method is Polymerase Chain Reaction (PCR)that amplify segments of DNA linked to heritable traits such as yield or diseaseresistance.

3 This method is useful because the DNA that we amplify is different(polymorphic) between cultivars. It is this difference that we use to determinewhether the plant has the desired trait or not. The process in which thedifferential DNA sites (or primer sites) are explored, comes from genetic mappingtechniques, RAPD, microsatellites etc. With a marker assisted selectionbreeding program the simpler methods are necessary since they are time andcost effective. PCR is an effective method for generating large quantities of aspecific DNA sequence from a small amount of starting DNA. This techniqueis useful for a MAS breeding program because the results are learn how MAS works, basic Molecular biology principles need to beunderstood.

4 The present bulletin Molecular Markers in crop Improvement has been designed to provide a basic understanding with regards to use ofmolecular Markers in crop Improvement . This bulletin describes basic conceptsused in marker assisted breeding programme, different applications of MASand basic principles underlying DNA extraction, PCR, running of gel and dataanalysis. The help rendered by Shri Diwakar Upadhyaya in editing the manuscriptis duly acknowledged. We hope that this bulletin will be of immence use forstudents and trainees of Molecular of Molecular Markers in Breeding of Basic Cited491 Basic ConceptsDuring the past 20 years there has been rapid growth in the relatively new field of plantbiotechnology and its associated techniques.

5 These have application, not only for the manipulationof biological systems for the benefit of mankind, but also to undertake studies for better understandingof the fundamental life processes. Consequently, it has become the fastest and most rapidly growingtechnology in the world. Biotechnology is defined as any technique that uses living organisms(or parts of organisms) to make/ modify products, to improve plants and animals or to developmicroorganisms for specific uses . It offers efficient and cost-effective means to produce anarray of novel, value-added products and tools. It has the potential to increase food productivity,reduce the dependency of agriculture on chemicals, lower the cost of raw materials and reduce thenegative environmental impacts associated with traditional production breeding is a dynamic area of applied science.

6 It relies on genetic variation anduses selection to gradually improve plants for traits and characteristics that are of interest for thegrower and the consumer. Another important way of Improvement is the introduction of new geneticmaterial ( , genes for biotic and abiotic stress resistance) from other sources, such as gene bankaccessions and related plant species. Although, current breeding practices have been very successfulin producing a continuous range of improved varieties, recent developments in the field of molecularbiology can be employed to enhance plant breeding efforts and to speed up cultivar biotechnology provides new tools that can facilitate development of improved plant breedingmethods and augment our knowledge of plant genetics.

7 The discovery of restriction enzymes bySmith and Wilcox, and the polymerase chain reaction (PCR) by Kerry Mullis and his group hascreated opportunity to understand the composition of organisms at the DNA level, and obtain a so-called genetic fingerprint. These studies are routinely done by the separation of DNA-fragments ona gel that results from a selective digestion of DNA with enzymes or from a selective amplificationof DNA using PCR. DNA fragments that result in different gel patterns between samples orindividuals are called polymorphic Markers . The visible differences on the gel result from differencesat the DNA level.

8 Not all types of Markers are the same; the information content depends on themethod that is used to obtain the marker data and the population in which the Markers were scored . Advanced tools for the retrieval of marker data and the subsequent analysis have beendeveloped that allow quick and reliable results in most plant (DNA) Markers are segments of DNA that can be detected through specificlaboratory techniques. For detection of Markers , either restriction enzymes or Polymerase ChainReaction (PCR) or their combination are used to generate/amplify the DNA sequences that arelinked to a heritable trait such as yield or disease resistance.

9 With the advent of marker -assistedselection (MAS), a new breeding tool is now available to make more accurate and useful selectionsin breeding populations. The objective of this section is to introduce genetic terminologies andconcepts associated with Molecular alternative form of a given allelic pair - tall and dwarf are the alleles for the height of apea plant. More than two alleles can exist for any specific gene, but only two of them will be foundwithin any diploid individual. In terms of Molecular marker the variant of a DNA sequence isreferred as an allele. An allele defined by Molecular means should have exactly the same geneticproperties as a phenotypically defined allele.

10 Molecular alleles should segregate by the same Mendelianprinciples as phenotypic alleles. Mostly, Molecular alleles are selectively neutral. Theories of populationgenetics apply to Molecular alleles as is the cross of an F1 hybrid to any one of the homozygous is the cross of any individual to a homozygous recessive parent. It is used to determine ifthe individual is homozygous dominant or lineAn individual that breeds true to type for a particular trait. This was an important innovationbecause any non-pure (heterozygous parents) would confuse the segregation ratio in individual which contains only one allele at the allelic pair, for example TT is homozygousdominant and tt is homozygous recessive.


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