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Science 9 Q1 M4
Science 9 Q1 M4
Science 9
First Quarter
Module No. 4 of 6
Non-Mendellian Patterns of Inheritance
Writer: Roland R. Agra
HONOR CODE
AS A MEMBER OF THE NAMUAC ACADEMY EAGLES FAMILY, I WILL CONDUCT
MYSELF WITH INTEGRITY & SINCERITY AT ALL TIMES, DEMONSTRATE COMPASSION &
JUSTICE IN ALL MY ACTIONS, UPHOLD THE VALUE OF EXCELLENCE, AND ABIDE BY THE
EXPECTATIONS SET FORTH IN THE STUDENT HANDBOOK.
I MAKE THIS PLEDGE IN THE SPIRIT OF HONOR & TRUST.
GOAL To perform an instrumental piece about caring for the respiratory and
circulatory systems
ROLE Song Writer, health advocate, performer
EXPECTATIONS
In Grade 8, you have learned that traits can be dominant or recessive through Gregor Mendel’s
study on the characteristics of the pea plants. Dominant traits are characteristics that are expressed in
an organism. On the other hand, recessive traits are characteristics that are hidden/not expressed in an
organism. Traits are the physical features of an individual. And these are passed from one generation to
another through genes.
Genes are segments of DNA coding for a specific trait. A dominant trait is expressed when a
dominant gene masks the recessive gene. So, the question is, are all traits controlled by a dominant or
a recessive gene? What about those traits that have more than two phenotypes? Do they follow
Mendelian patterns of inheritance?
But not all traits are controlled by alleles found in the body chromosomes (autosomes). There
are traits governed by the sex chromosomes. These traits are called sex-linked traits. Sex-linked traits
affect both males and females. But in some cases, one particular sex is more prone to have a sex-linked
trait.
PRE-TEST
Directions: Choose the letter of the correct answer. Write your answers beside the number.
5. In ABO Blood Group system, O is recessive. Therefore, for this blood type to be
expressed, ___________.
a. Two O alleles must be present.
b. One O allele and 1 B allele must be present.
c. The alleles A, B and O must all be present.
d. The alleles A, B and O must all be present.
OVERVIEW
In Grade 8, you learned that cells divide to produce new cells and meiosis is one of the processes
producing genetic variations in Mendelian patterns of inheritance. In Grade 9, you will focus on describing
the location of genes in chromosomes, explain the different patterns of non- Mendelian inheritance and
describe the molecular structure of the DNA.
Father Gregor Johann Mendel’s principles form the base for the understanding of heredity and
variation. Although Mendel’s work failed to discuss thoroughly the ‘factors’ or genes he mentioned in his
laws of inheritance, his findings prompted other scientists to probe further into the mystery of heredity.
Several researches were conducted after the rediscovery of Mendel’s work.
Walter Sutton and Theodore Boveri became popular because they found the best evidence that
an inherited trait is determined by chromosomes. Chromosome Theory of Inheritance explained that
genes are in the chromosomes.
Mendelian laws of inheritance have important exceptions to them. For example, not all genes
show simple patterns of dominant and recessive alleles.
LESSON PROPER
To determine the phenotypes of the offspring, a Punnett square is used. A Punnett square is a
tool used to determine the chance of inheriting a specific trait.
A genotype is an individual's collection of genes. In the example that follows, RR and WW are
the possible genotypes of a four o’clock flower. When a true-breeding, pure red-flowered four o’clock
plant (represented by RR) crosses with a true-breeding, pure white-flowered four o’clock plant
(represented by WW), their offspring are all pink-flowered plants (represented by RW) which are
heterozygous. They neither produced red nor white-flowered plants because neither of the two is
completely dominant.
In incomplete dominance, one-half of the gametes of the heterozygotes (pink flowers) carry the
allele for the red flower and the other one-half of it carry the allele for the white flower. Thus, the results
of a heterozygote self-cross can still be predicted both the genotypic and phenotypic ratios is 1:2:1. In
this case, the genotypic ratio would be 1 RR: 2 RW: 1 WW, and the phenotypic ratio would be 1:2:1
for red: pink: white.
Examples of this include petal coloration in some flower species (such as carnations and four
o’clock flowers), curliness of human hair, and human hypercholesterolemia (also called high cholesterol,
is the presence of high levels of cholesterol in the blood).
Lesson 2: Codominance
The second non-Mendelian pattern of inheritance is the law of codominance. It states that both
alleles are expressed equally in the phenotype of the heterozygote. It means to say that both traits are
observed. Thus, a third phenotype is expressed.
One typical example is the coloration of the cow and bull. A red cow results in an offspring with
both red and white hairs called roan. Roan refers to cows with red hair and white blotches and usually
codominance occurs in animals.
In cattle, there are 3 different phenotypes. Those with red coats are homozygous for the red coat
allele. Those with white coats are homozygous for the white coat allele. Lastly, those cattle with red hairs
mixed with white hairs are said to be heterozygous and appears roan. The appearance of roan coats is
due to the codominance of the red and white coat color alleles.
In summary:
Cattle and Horse Coat Color
Genotype Resulting Phenotype
CRCR Red coat
CWCW White coat
CRCW Roan coat (red hairs mixed with white)
Therefore, the trait is neither dominant nor recessive. Just like in incomplete dominance, the
genotypic ratio becomes the phenotypic ratio. Examples of this include A and B blood types in humans,
sickle-cell disease, and coat color in cattle and horses.
The work of Mendel on garden peas and his proposal on his genetic laws suggested that a
specific gene is controlled by just two alleles. In our case today, we can say that it’s not always the
situation. Multiple alleles may exist in a population level and different individuals in the population may
have different pairs of alleles despite the fact that humans and other diploid organisms can only have two
alleles controlling a gene.
In humans, the ABO Blood Group system is a character governed by multiple alleles. There are
3 alleles that governed this system: IA, IB and i.
In summary:
Phenotypes Genotypes Phenotypes Genotypes
Type A I I (homozygous), IAi (heterozygous)
A A Type AB IAIB
Type B IBIB (homozygous), IBi (heterozygous) Type O ii
Humans have 46 chromosomes in each cell. Observation of the human body cells shows
23 pairs of chromosomes for both males and females. Twenty- two pairs are somatic
chromosomes. The 23rd pair consists of sex chromosomes. Human males and some other male
organisms, such as other mammals and fruit flies, have non-identical sex chromosomes (XY).
Females have identical (XX) sex chromosomes while males have the XY sex chromosomes.
Let us study gamete formation based on the sex chromosomes. You will observe in Figure 3 that
all egg cells receive an X chromosome; while half of the sperm cells receive X chromosomes and the
other half receive Y chromosomes.
Male
Male
Female
Sex chromosomes Female
XX
XX
XY XY
Meiosis
X X X Y
Gametes
Gametes
X X
If an egg is fertilized by a sperm with a Y chromosome, as shown in the figure, the offspring is
male. When an egg is fertilized by a sperm carrying an X chromosome, the offspring is female. Note that
there is a 50 percent chance of having a male or female offspring. The greater the number of offspring,
the greater is the chance of getting the expected 1:1 ratio of male and female.
Key Concepts
Males have 44 body chromosomes and two sex chromosomes X and Y. The males
determine the sex of their children. Females have 44 body chromosomes and two sex
chromosomes, both X. The total number in each cell of an individual is 46. These chromosomes
contain the genes, which arethe factors of heredity.
Genes located on the X chromosomes are called X-linked genes. Genes on the Y chromosomes
are called Y-linked genes. An example of an X-linked trait is color blindness. To illustrate the inheritance
of an X-linked trait, we will use color blindness in our discussion. Let us study the table below. The X
chromosome with the gene for color blindness is represented as XC, while the one without is represented
as X.
Can you identify the genotype of the female who is color-blind? Notice that for a female to
become color-blind, she must be homozygous (XC XC) for
the color-blind genes. The trait is, therefore, recessive in
females. If a female has only one X chromosome with the
allele for color blindness, she becomes normal but can pass
on the trait to her offspring. She is therefore a carrier of the
trait. Since males have only one X chromosome, the gene
for color blindness when present in the male, will always be
expressed because it does not have an allele to hide or
prevent its expression. Thus, the male will be color- blind.
This is the reason why color blindness is more common in
males than in females.
Another example of an X-linked trait in humans is hemophilia. A person suffering from hemophilia
could die from loss of blood even from a small wound because the blood either clots very slowly or does
clot at all.
An example of a Y-linked trait, hypertrichosis pinnae auris, a genetic disorder in humans that
causes hairy ears. Since the trait is found in the Y chromosome, then only males can have the trait. A
father who has the condition will pass it on to all his sons, and they, in turn, will pass it on to their own
sons.
If you look at the heterozygous gene pair for baldness (Bb), males express baldness, while
females do not. Baldness may be expressed in females but it occurs more frequently in males. Such trait
is sex-influenced because of a substance that is not produced equally in males and females.
Key Concepts
Sex-linked traits are inherited through the X chromosomes. Males have only one X
chromosome. Thus, if they inherit the affected X, they will have the disorder.
Females have two X chromosomes. Therefore, they can inherit/carry the trait without being
affected if it acts in a recessive manner. Sex-limited traits are those that are expressed
exclusively in one sex. Sex-influenced traits are expressed in both sexes but more frequently in
one than in the other sex.
WRAP- UP
✓ Incomplete dominance occurs when the phenotype of the offspring is somewhere in between
the phenotypes of both parents; a completely dominant allele does not occur.
✓ Codominance occurs when both alleles are expressed equally in the phenotype of the
heterozygote.
✓ Many genes have multiple (more than two) alleles. An example is ABO blood type in humans.
There are three common alleles for the gene that controls this characteristic. The alleles IA and
IB are dominant over i. Another example is the coat color of rabbits.
VALUING
Look at the picture, what will happen if there is an alteration of the genetic make-up
of an organism? What could be its effect on the organism? Observe the picture below.
If the genetic make-up of an organism is altered, mutation will take place. Mutation
is alteration in one’s genetic make-up. How will you inform people to help lessen the
occurrence of mutation?
POST-ASSESSMENT
A. Enrichment Activities
Read and analyze the given problem. Answer the questions that follow.Write your answers neatly in a
sheet of paper.
Problem: Two pink bougainvillea flowers were crossed and they produced offspring with 3
different colors. (RW is the allele for color pink while RR is the allele for color red and WW is
the allele for color white).
Questions:
1. What would be the phenotypes of the offspring? _____________________________
Activity 2. Codominance. A Red Bull (RR) and a white cow (CC) mated. Predict for the possible
offspring ofthe crossbreeding by using a Punnett square.
Questions:
1. What would be the phenotypes of the offspring? _____________________________
Activity 3. Multiple Alleles. Let us try to show the cross between a wife with Type B heterozygous blood
type and the husband with homozygous blood type A.
FEMALE
MALE
Activity 4. When Gender Matters. Read the given problem: Color-blindness is a recessive, sex-linked
disorder in humans. A color-blind man has a child with a woman who is a carrier of the disorder.
1. Illustrate using a Punnett square the probability of having children who will have normal vision
and children who will be color-blind.
Guide Questions:
1. What is the genotype of the male?
2. What is the genotype of the female?
3. What is the chance that the child will be color-blind?
4. What is the chance that a daughter will be color-blind?
5. What is the chance that a son will be color-blind?
B. Post Test
Multiple Choice: Select the letter of the best answer from among the given choices. Write it on a separate
sheet of paper.
1. The blending of colors among the bougainvillea flowers (Bougainvillea glabra) is an example of what
pattern of non-Mendelian Inheritance?
a. Codominance b. Multiple Alleles
c. Incomplete Dominance d. Both B and C
5. What is the phenotypic and genotypic ratios in incomplete dominance and codominance?
a. 2:2
b. 3:1
c. 1:2:1
d. 1:3:0
6. If one of your parents is blood type A and the other is type B, which of the following blood types
would you likely be?
a. A c. B
b. AB d. O
7. A black chicken and a white chicken mate and produce a gray chick. Which type of inheritance
would this be an example of?
a. Recessive
b. Dominance
c. Codominance
d. Incomplete dominance
9. Which among the following conditions of parents will have a child that is hemophiliac?
a. When both her parents are hemophiliac.
b. When both her parents are normal (not hemophiliac).
c. When her father is normal and her mother is hemophiliac.
d. When her father is hemophiliac and her mother is normal (not hemophiliac).
10. A colorblind female marries a man with a normal color vision. What is the probability that any of their
children will become colorblind?
a. 0%
b. 25%
c. 50%
d. 75%