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8 Sep 2005 18:28:52 -0000

Marker Assisted Selective Breeding

press-release

 

 

 

 

 

The Institute of Science in Society Science Society

Sustainability http://www.i-sis.org.uk

 

General Enquiries sam Website/Mailing List

press-release ISIS Director m.w.ho

 

This article can be found on the I-SIS website at

http://www.i-sis.org.uk/MAS.php

========================================================

 

 

ISIS Press Release 08/09/05

 

Marker Assisted Selective Breeding

******************************

 

Prof. Joe Cummins gives the current state

of play in how molecular genetic analysis can aid in

selective breeding without genetic modification

 

The fully referenced version of this article is posted on

ISIS members' website

http://www.i-sis.org.uk/full/MASFull.php.

Details here

http://www.i-sis.org.uk/membership.php

 

Quantitative traits not determined by single genes

Genetically modified (GM) crops are based on inserting

synthetic foreign genes mainly from bacteria, to impart

herbicide tolerance or insect resistance into the genomes of

crop plants. This technology has so far provided little if

any increase in yield, stress tolerance or long-term

resistance to microbes or nematodes. Traditional breeding of

crops and animals has been based on the use of genetic

markers that are inherited. The main agricultural traits

governing yield (or size), stress resistance or long-term

disease protection are quantitative trait loci (QTL, `loci'

is another word for genes). One of the founders of the study

of population genetics, Ronald A. Fisher, described QTL as

many independent loci that added together to determine

traits such as size [1]. QTL are seldom tightly linked on a

chromosome and the loci are dispersed over many chromosomes

in the genome. Selection of QTL traits has been inherently

slow and meticulous, but has resulted in major improvements

to crops and livestock.

 

While Fisher believed that QTL were made up of very many

genes each adding small increments to a trait, recent

findings indicate that some QTL may be made up of a

relatively small number, say twenty or so, genetic markers

that could be easily selectedprovided they could be

identified. Currently, it appears that many QTL may have

relatively few loci but some important QTL may be closer to

the very large number of genes envisioned by Fisher, in

which case, identifying and selecting such traits by the

molecular markers are unlikely to be cost-effective.

 

Molecular markers can be used to aid selective breeding

There is a growing arsenal of molecular markers

(polymorphisms) that aid in identifying QTL and selecting

them for crop and animal enhancement. The process ofusing

such markers is called marker-assisted selection (MAS),

which differs from genetic modification because the genes

being selected for crop or animal improvement are not

altered in any way. The molecular markers used in selection

are probed using sequences from a gene bank and identified.

The markers used to probe the progeny of a cross are not the

QTL genes themselves but they are close to the QTL on the

genetic map. Of course the markers can be used to determine

the molecular identity of the QTL, but the molecular marker

is used even when the QTL is identified because the marker

is cheaper and quicker to use to identify a large number of

progeny. Recombination may separate the marker from a QTL,

but the closer the marker is to the QTL, the more remote is

the chance of separation by recombination. The more

polymorphic markers available for a breeding programme, the

more effective it will be.

 

There are several types of mk but requires a relatively

large amount of DNA and is rather expensive in a large

screening program [2]. RAPD utilizes low stringency

polymerase chain reaction (PCR) amplification with single

primers of arbitrary sequence to generate strain-specific

arrays of anonymous DNA fragments [3]. The method

requiresolecular markers used in MAS; these include

restriction fragment length polymorphism (RFLP), random

amplification of polymorphic DNA (RAPD), amplified

restriction fragment length polymorphism (AFLP), single

sequence repeats (SSR) and single nucleotide polymorphisms

SNPs [2]. RFLP involves the use of restriction enzymes to

cut chromosomal DNA at specific short restriction sites,

polymorphisms result from duplications or deletions between

the sites or mutations at the restriction sites. RFLP

provided the basis for most early wor tiny DNA samples and

analyses a large number of polymorphic loci [2]. AFLP

requires digestion of cellular DNA with a restriction

enzyme, then using PCR and selective nucleotides in the

primers to amplify specific fragments [4]. The method

measures up to 100 polymorphic loci and requires a

relatively small DNA sample for each test [4]. SSR analysis

is based on DNA micro-satellites (short-repeat) sequences

that are widely dispersed throughout the genome of

eukaryotes, which are selectively amplified to detect

variations in simple sequence repeat [5]. SSR analysis

requires tiny DNA samples, and has a low cost per analysis

[2]. SNPs are detected using PCR extension assays that

efficiently pick up point mutations [6]. The procedure

requires little DNA per sample and costs little per sample

once the method is established [2]. One or two methods are

used in a typical MAS breeding programme.

 

MAS has been employed in breeding cereals, and extensively

so in maize breeding. Corporations including Monsanto and

Syngenta have invested heavily in the programme. SNP appear

to be the dominant marker for selection. Wheat has seen

less progress in MAS than maize, but there is good success

in the area of quantitative disease resistance. Rice has

also seen extensive activity in MAS centering on pyramiding

disease resistance genes. SNPs appear to be identified for

all the major cereals [7]. MAS is being used to improve

forage crops through QTL for nitrogen use efficiency, and

there was a strong response [8]. The pome fruits, apple and

pear, have extensive MAS programmes, mainly based on RFLP,

RAPD, SSR and AFLP. The traits being selected include fruit

production, storage and disease resistance [9]. A global

strategy using MAS for livestock genetic improvement in the

developing world was proposed. QTL mapping would be used in

genetic improvement and to bring together desirable traits

from around the world [10]. It has been proposed that

assessment of genetic markers will greatly enhance the

conservation of genetic diversity in wild crop relatives

[11], and the information from wild crop relatives could be

directly employed in MAS of the crop plant.

 

Does MAS actually work? A recent review by William Hill of

Edinburgh University focused on the QTLs for oil production

in maize and for body size in chickens. In neither case

could individual QTL with substantive quality be detected.

Instead, identified QTLs created small additive increments

that could be selected, but only with patience [12]. Hill's

report suggested that Fisher's view of QTLs prevailed and

that the use of MAS might not be cost-effective. It may be

that MAS is effective in traits such as disease resistance

and certain agronomic performance but that important traits

such as oil production in maize or body size in chickens are

most effectively bred using traditional selection methods.

 

Farmers in developing countries and even some farmers in the

developed world face the growing control of seed production

by a few multinational corporations. One solution has been

to help the farmer breed varieties tuned to the local

environment and free of the greedy demands of seed

corporations. It is highly unlikely that indigenous farmers

will take to MAS and molecular genomics. However, those

scientists working with indigenous farmers would recognize

markers linked to valuable agronomic traits and pass on that

knowledge to the indigenous plant breeders to assist them in

making selections that are beneficial.

 

In the long run it seems likely that MAS will play an

important role in plant breeding, even though it may not be

as large as has been claimed by advocates. MAS should not

affect organic certification because transgenes are not

introduced into the crop. Molecular genetics is used only in

analyzing the crosses. Nevertheless, MAS has far more to

offer in crop and animal improvement than genetic

modification.

 

 

 

========================================================

This article can be found on the I-SIS website at

http://www.i-sis.org.uk/MAS.php

 

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General Enquiries sam Website/Mailing List

press-release ISIS Director m.w.ho

 

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