5.

GENE INTERACTIONS:

The phenomenon of two or more genes governing the development of a single

character in such a way that they affect the expression of each other in various ways is
known as gene interaction.
When one gene affects in any way the expression of another gene, the
phenomenon is called epistatis. Thus all cases of gene interaction are examples of
epistatis. But sometimes the term epistatis has been used to denote the masking effect
of one gene on the expression of another gene.
There are several types of gene interaction. Some of the common gene
interactions are as follows:
1. Typical dihybrid ratio for a single trait (9:3:3:1)
2. Duplicate gene action (15:1)
3. Complementary gene action (9:7)
4. Supplementary gene action (9:3:4)
 5. Inhibitory gene action (13:3)
6. Masking gene action (12:3:1)
7. Polymeric gene action (9:6:1)
8. Additive gene action (1:4:6:4:1)
1) Typical dihybrid ratio for a single trait (9:3:3:1)
This type of gene interaction produces the typical di-hybrid ratio of 9:3:3:1 in
F2 for a single character. Evidently the concerned character is governed by two genes
showing complete dominance.
In case of chickens or fowls, comb shape is governed by two genes. While one
gene gives rise to rose comb, another gives rise to pea comb. Each of these two is
dominant over single comb. However, when both are brought together, a new
phenotype ‘walnut’ appears.
As worked out by Bateson and Punnett, when both dominant alleles are present
‘walnut’ phenotype appears and when both recessive alleles are present ‘single’ comb
appears. ‘Rose’ and ‘Pea’ phenotypes appear due to the presence of different single
dominant alleles. If pea (rrPP) and rose (RRpp) are crossed, F1 birds showed ‘walnut’
comb as it has the dominant alleles of both the genes P and R.
Later on, when the F1 walnut combed birds were inbred together, in F2 generation
there appeared walnut, rose, pea and single combed fowls. These types occurred in the
proportions; 9/16 walnut, 3/16 rose, 3/16 pea and 1/16 single.
The mode of inheritance of the genes for ‘rose’ and ‘pea’ does not differ at all from
the usual Mendelian scheme. The differences that distinguish this and similar cases
from simple di-hybrid inheritance are that (i) the F1 does not resemble with parents
and (ii) apparently new or unusual characters (walnut) results from an interaction
between two independently inherited genes, and the other (single comb) results from
the interaction of their two recessive alleles. These peculiarities are not due to a new
method of inheritance but simply to the fact or circumstance that both genes involved
happen to express themselves in this case (fowl comb).

2) Duplicate gene action (15:1):

The two pairs of factors which have identical effect are known as duplicate
factors. Or Characters showing duplicate factor or gene action are governed by two
dominant factors. These dominant factors produce the same phenotype whether they
are alone or in pairs. (Awned and awnless characters in rice plants)
Genotypes and phenotypes of F2 generation:
 Thus, in duplicate gene action, the presence of a single dominant allele of any
one of two genes governing the dominant phenotype e.g., awned type in rice, while
the recessive phenotype e.g., awnless is produced only when both the genes are in the
homozygous recessive condition.
A similar case of duplicate factor interaction governs the fruit shape in Bursa,
endosperm colour in maize, nodulation in groundnut and certain characters in many
other plants. First of all, the duplicate gene interaction was observed and explained by
G.H. Shull in plant called shepherd’s purse (Capsella bursapastoris.)
3) Complementary gene action (9:7):
In sweet pea (Lathyrus odoratus) two varieties of white flowering plants were
seen. Each variety bred true and produced white flowers in successive generations.
According to Bateson & Punnett, when two such white varieties of sweet pea were
crossed, the offspring were found to have purple coloured flowers in F1 but in
F2generation 9 were purple and 7 white. This is again a modification of 9:3:3:1 ratio,
where only one character i.e., flower colour is involved.
It is clear in the above example that for the production of the purple flower
colour both complementary (C and P) genes are necessary to remain present. In the
absence of either genes (C or P) the flowers are white.
Thus, it is clear that genes C and P interact and presence of both is essential
for the purple colour in the flower. These types of genes in which one gene
complements the action of the other gene, constitute complementary genes or factors.
(Complementation between two non-allelic genes (C and P) are essential for
production of a particular or special phenotype i.e., complementary factor)
 Genotypes and Phenotypes of F2 and breeding behaviour expected in F2 of
complementary factors:

Aleurone colour in maize is also controlled by complementary genes.

4) Supplementary gene action (9:3:4):
Here only one factor is sufficient to produce a phenotypic expression but
addition of another factor causes the change in expression.
Or
Supplementary genes are two independent dominant genes interacting to
produce a phenotypic expression different from that produced by either gene alone.
Or
In supplementary gene action, the dominant allele of one gene is essential for
the development of the concerned phenotype, while the other gene modifies the
expression of the first gene. For example, the development of grain colour in maize is
governed by 2 dominant genes ‘R’ and ‘P’.
The dominant allele ‘R’ is essential for red colour production; homozygous
state of the recessive allele ‘r’ (rr) checks the production of red colour. The gene ‘P’ is
unable to produce any colour on its own but it modifies the colour produced by the
gene ‘R’ from red to purple. The recessive allele ‘p’ has no effect on grain colour.
Showing genotypes and phenotypes of F2 behaviour of supplementary factors in
grain colour of maize:

Examples of supplementary factors have also been seen in other plants and
animals too. For instance, it is clearly visible in skin colour of house mouse and
guinea pigs. When black mice are crossed with ordinary albinos, the progeny are
usually all agouti like the wild type. When these F1 agouties are inbred, their
progeny consists of 9/16 agouti, 3/16 black and 4/16 albino animals.

5) Inhibitory gene action (13:3):

In this type of modification two pairs of genes are involved and one of the
non-allelic dominant gene inhibits the expression of the other non-allelic dominant
gene.
Or
A gene which inhibits the expression of an active allele situated at different
locus is called as inhibitory gene. Thus, in inhibitory gene action one dominant
inhibitory gene prevents the expression of another dominant gene. Example of
inhibitory gene is pigmentation in rice plants. In rice plants, the presence of gene
‘P’ is responsible for deep purple leaves. But if a gene ‘I’ is present then the
expression of purple leaf colour is inhibited and the leaf becomes normal green.
Thus, in a cross, between green (IIpp) and purple (iiPP), all the off springs in F1 are
green but in F2 progeny, green and purple are obtained in ratio of 13:3. This
modifies the typical 9:3:3:1 F2 ratio in to a 13:3 ratio.
 It is now well understood that pigmentation in rice plant is governed by two
non-allelic genes. ‘P’ gene produces purple colour while its recessive ‘p’ green
colours. Another dominant gene ‘I’ which produces green colour in rice plants,
inhibits or prevents the colour production by ‘P’ when both ‘I’ and ‘P’ are present
together.
The recessive alleles ‘I’ is ineffective and does not affect the colour
production in any way in rice plants. Other examples of inhibitory gene action are
the development of feather colour in fowls, seed colour in maize etc. Bateson and
Punnett for the first time made the discovery of Inhibitory gene in fowls.
 Genotypes and phenotypes of F2 generation:

6) Masking gene action (12:3:1): also known as epistatic gene action.

The term “epistatis” was first used by Bateson (1909). It is the interaction
between non-allelic genes in which one gene suppresses the expression of other
gene. A gene that hides or masks the expression of another non-allelic gene is
called as epistatic factor and the gene that is hidden or suppressed is said to be
hypostatic.
This phenomenon of masking one gene by another non-allelic gene is
known as epistatis and is similar to dominance, except that it occurs between non-
allelomorphic genes, instead of comprising allelomorphic genes. Such a gene
interaction has been also named as masking gene action.
In Cucurbita pepo, there are 3 types of fruit colour- (i) White (ii) Yellow
and (iii) Green. White is found dominant over yellow as well as green colour.
When yellow is crossed with green, yellow is found to be dominant. Here, the
character (colour of fruit) is governed by 2 pair of genes-

White x green → White dominant

Yellow x green → Yellow dominant

Here white is dominant factor and yellow is hypostatic factor.

White x Yellow → White dominant.

If white dominant is represented by ‘W’ and its recessive by ‘Y’, both non-allelic
factors or genes may be represented as follows-

7) Polymeric gene action (9:6:1):

When two genes govern any character separately, their effect is equal but when
both the genes are present together, there phenotypic effect is increased or raised as if
the effects of the two genes were additive or cummulative. It is notable in this case that
both the genes show complete dominance. “Additive or cummulative effect of genes
present at different loci is called polymerism.”
In wheat three types of pericarp colour is found:
(i) Deep red (ii) Light red and (iii) Colourless. When a cross is made between
plants having deep red (AABB) and colourless (aabb) pericarp, the F1 (AaBb) has deep
red pericarp due to the additive effect of both the genes A and B.
In F2 generation, on an average, 9/16 plants will have dominant alleles of both
the genes A and B; as a result these plants will produce deep red per-carp. 6/16 plants
will have light red pericarp since they have either A or B, but not both. The rest 1/16
plant will be homozygous recessive for both the genes and will be therefore, colourless.

Genotypes and phenotypes of the F2 generation:

Thus, polymerism interaction modifies the typical 9:3:3:1 ratio in to 9:6:1 ratio. Other
examples of polymerism interaction are also known, e.g., fruit shape in summer
squash etc.

8) Additive gene action (1:4:6:4:1):

In additive gene action, each positive allele of the two genes governing a trait
produces equal and identical effect on the character. The effects of all the positive
alleles present in an individual at the two loci are additive. As a result, the 9:3:3:1
dihybrid F2 ratio is partitioned into the 1:4:6:4:1 ratio. This gene action is the basis for
the multiple factor hypothesis of Nilsson-Ehle. Therefore, the genes showing additive
gene action are called multiple factors or more commonly, polygenes. Each polygene
has two alleles. One allele of each polygene produces a positive effect in the character
governed by the gene; this is called positive allele. The other allele of each gene has
no effect on the character, and is known as negative allele. The positive alleles are, as
a convention, denoted by capital letters, while negative alleles are given the respective
small letters as symbols. However, this notation does not indicate a dominance of the
positive alleles over the negative ones.
For example, seed colour in tetraploid wheat is governed by two polygenes R1
and R2. The positive alleles of these two genes, viz., R1 and R2, produce colour. Their
negative alleles, namely, r1 and r2, do not produce any colour. Each R1 and R2 allele
produces a small amount of colour. The effects produced by all the R1 and R2 alleles
are additive. Therefore, the total intensity of colour produced depends on the total
number of positive alleles of the two genes present. Thus, R1R1R2R2 produces dark
red colour, R1R1R2r2 generates medium dark red, R1r1R2r2, etc. Yield medium red and
so on. When a variety having dark red (R1R1R2R2) seeds is crossed with a variety
having white seeds (r1r1r2r2), F1 (R1r1R2r2) has medium red seeds, this is because F1
seeds only two positive alleles (one R1 and one R2). In the F2 generation one zygote
out of sixteen will have four positive alleles (R1R1R2R2). the seeds will be identical to
one of the parents, and will have dark red colour. In four (out of 16) seeds, three
positive alleles will be present (R1r1R2R2 and R1R1R2r2). These seeds will be lighter in
colour than the seeds of the dark red colour parent but darker than the F1 seeds; they
will be medium- dark red in colour. Six (out of 16) seeds will have only two positive
alleles each (R1r1R2r2, R1R1r2r2, r1r1R2R2). They will be identical to the F1 seeds
and medium red in colour. In four (out of 16) other seeds (R1r1r2r2, and r1r1R2r2), only
one positive allele will be present. The colour of these seeds will be light red. In the
remaining one seed (out of 16), there will be no positive allele (r 1r1r2r2). This seed will
be white in colour.

Parents R1R1R2R2 r1r1r2r2

Dark red white

R1R2 r1r2
Gametes

♀ ♂ R1R2 R1r2 r1R2 r1r2

R1R1R2R2 R1R1R2r2 R1r1R2R2 R1r1R2r2
R1R2
Dark red Medium dark red Medium dark red medium red
R1R1R2r2 R1R1r2r2 R1r1R2r2 R1r1r2r2
R1r2
Medium Dark red Medium red Medium red Light red
R1r1R2R2 R1r1R2r2 r1r1R2R2 r1r1R2r2
r1R2
Medium dark red Medium red medium red light red
R1r1R2r2 R1r1r2r2 r1r1R2r2 r1r1r2r2
r1r2
Medium red Light red light red white
 Thus the multiple factor hypothesis or the additive gene action is able to fully
explain the 1:4:6:4:1 ratio for seed colour in F2 generation of wheat and oat crosses.
Additive gene action is involved in the expression of quantitative traits. Qualitative traits
show a continuous variation. As a result, they can not be classified into two or more
separate classes. These characters are governed by polygenes. Genes with small
cumulative effects governing a single trait are known as polygenes. In contrast, genes
having a large effect on the characters they govern are called oligogenes or major genes.
Oligogenes generally govern qualitative traits with discrete variation. They permit
classification of individuals into few discrete classes for the characters they govern. All
the other cases of gene interaction described in this chapter are due to oligogenes.
Genotypic and phenotypic frequencies produced by the segregation of two genes,
R1 and R2, with cumulative effect on seed colour in wheat
genotype frequency Number of dominant alleles Phenotype frequency
R1R1R2R2 1 4 Dark red 1
R1r1R2R2 2 3 Medium dark red
4
R1R1R2r2 2 3 Medium dark red
R1r1R2r2 4 2 Medium red
R1R1r2r2 1 2 Medium red 6
r1r1R2R2 1 2 Medium red
R1r1r2r2 2 1 Light red
4
r1r1R2r2 2 1 Light red
r1r1r2r2 1 0 white 1