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Glossary Plant Breeding

a glossary for plant breeding practices and application

a glossary for plant breeding practices and application

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Genetic Male Sterility. A type of male sterility that is governed by the gene(s) carried

on the chromosomes. The male sterile condition is ordinarily monogenic recessive. Its

exploitation in hybrid seed production is rather difficult due to problems involved in

the maintenance of male-sterile line. Male-sterile stocks are maintained by crossing

with heterozygous male-fertile line (Ms ms). This necessitates identification of malesterile

(and male-fertile) plants since the progeny contains the two types in equal

proportions. To circumvent this problem, genetic markers such as tightly linked genes

or pleiotropic effects of male-sterile genes can be used.

Gene Pyramidying. A strategy for management of resistance that involves incorporation

of an increasing number of resistance genes into the same cultivars likely to be

released in succession. Thus, with the available number of genes, the resistance can

be used for a long time. However, there are several disadvantages that limit its use: (a)

considerable efforts are required to incorporate many a major gene into one

genotype, (b) the use of back cross method to incorporate the major genes into one

genotype restricts the agronomic characteristics of the new cultivar, and (c) resistance

of the cultivar may encourage evolution of new virulent races of the pathogen,

particularly if the same major genes are used singly in other varieties being grown in

the adjacent area.

Genetic Assortative Mating. Mating together of individuals more closely related (by

ancestry) than individuals mating at random. Genetic assortative mating at all loci is

called inbreeding. (Inbreeding deals with the entire genome whereas genetic

assortative mating is specific to a locus). It results in an increase in homozygosity.

Genetic Advance. The genetic superiority (and not phenotypic) of selected individuals /

lines/families over the base population. It measures the difference between mean

genotypic values of selected lines (As) and of the original lines (Ao). Thus, Gs = As –

Ao = k × σ P ×H 2 . Therefore, it depends on: k = standardized selection differential

and its value is fixed for a given proportion of lines saved from the base population

(2.06 at 5% selection intensity), σ P = phenotypic standard deviation of the original

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