12.07.2015 Views

marker-assisted selection in wheat - ictsd

marker-assisted selection in wheat - ictsd

marker-assisted selection in wheat - ictsd

SHOW MORE
SHOW LESS
  • No tags were found...

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

108Marker-<strong>assisted</strong> <strong>selection</strong> – Current status and future perspectives <strong>in</strong> crops, livestock, forestry and fishuntil some benefit is extracted from it.On the other hand, far too much efforthas been expended <strong>in</strong> the identification of<strong>marker</strong>s for traits without carry<strong>in</strong>g thesethrough to application. Often gene tagg<strong>in</strong>gis a component of a short-term project, anddoes not receive the necessary follow up <strong>in</strong>implementation. In each case, the essentialquestion is: what are the key genes foreach crop? And once def<strong>in</strong>ed, which genesmerit the <strong>in</strong>vestment to develop molecular<strong>marker</strong>s? For <strong>in</strong>vestments <strong>in</strong> molecular<strong>marker</strong> development to yield results, itis important that traits are chosen forwhich molecular breed<strong>in</strong>g has both a clearadvantage over field-based <strong>selection</strong> and isfeasible <strong>in</strong> the short to medium term. It isalso important that emphasis be given toselect<strong>in</strong>g the relevant crosses, pedigrees andpopulations <strong>in</strong> which to practise MAS, andto have <strong>in</strong> place appropriate phenotyp<strong>in</strong>gstrategies for the confirmation of MASresults. In this regard, the use of parentalsurveys of many of the genotypes <strong>in</strong>volved<strong>in</strong> a given breed<strong>in</strong>g programme is animportant first step <strong>in</strong> implement<strong>in</strong>g MAS.Short- and long-term research relatedto MASThe present research structure that is normallybased on short-term projects, usuallyof three years’ duration, can seldom beexpected to deliver results of usable <strong>marker</strong>sfor complex traits. Such short-term projectsthat seek to establish the basis for MASor to implement <strong>selection</strong> should limittheir objectives to simply <strong>in</strong>herited traits.On the other hand, longer-term fund<strong>in</strong>geither of a programmatic or successiveproject fund<strong>in</strong>g nature, must be obta<strong>in</strong>edto address more complex traits governedby QTL as these would normally requireat least two phases of three-year projects.The first phase might be expected to revealthe <strong>in</strong>heritance of a given trait, establish<strong>in</strong>gthe location and numbers of QTL, while asecond phase would be required to validatethese over more environments and to f<strong>in</strong>d<strong>marker</strong>s that are polymorphic over a widenumber of genotypes and therefore widelyuseful for breed<strong>in</strong>g, as well as adapted torapid laboratory techniques. A mediumtolong-term <strong>in</strong>vestment likewise impliescareful prioritization of such traits, withregard to potential impact and the eventualneed for MAS. These reflections are basedupon presently available laboratory techniques,but as techniques for more detailedand widespread evaluation of loci and genotypesare developed (e.g. gene chips foranalysis of multiple loci), conclusions couldchange significantly.Scal<strong>in</strong>g-up technologiesAfter the development of molecular <strong>marker</strong>sfor a trait and their <strong>in</strong>itial implementation,a period of scal<strong>in</strong>g-up <strong>in</strong> use of the specific<strong>marker</strong>s is necessary. Sometimes this<strong>in</strong>volves changes to MAS protocols, <strong>in</strong>the <strong>marker</strong> detection technique or <strong>in</strong> the<strong>marker</strong>s themselves. Marker re-design hasbeen a common element of scal<strong>in</strong>g-up exercisesand can <strong>in</strong>volve someth<strong>in</strong>g as simpleas chang<strong>in</strong>g a PCR fragment size to implement<strong>in</strong>ga SNP assay for the actual sequencedifferences between alleles. Technologiesthat speed up the implementation processand lower the costs associated with scal<strong>in</strong>gupare crucial to the success of MAS and areoften neglected.Development of <strong>marker</strong>s that areuseful <strong>in</strong> a large number of crossesOften a <strong>marker</strong> developed for a particulartrait <strong>in</strong> one or a few related genotypes willnot work for other genotypes with highvalue of the trait due to differences <strong>in</strong> geneor allelic effects. Unravell<strong>in</strong>g the genetics of

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!