Module 1
Module 1
Module 1
CAS NS 3b - Genetics
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PRESIDENT RAMON MAGSAYSAY STATE UNIVERSITY
NOT FOR SALE
CAS NS 3b - Genetics
First Edition, 2021
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Evaluators:
Course Overview
Introduction
This course covers fundamental understanding of how physical and physiological traits are
inherited and the chemical structures that influence those traits. It also focuses on physical
basis of inheritance, Mendelian and non-Mendelian (or transmission) genetics, molecular
genetics, mutation, human and behavioral genetics.
At the end of the lecture course, the students should be able to:
At the end of the laboratory course, the students should be able to:
1. Develop the ability to explain concepts using models during online laboratory class
demonstration;
2. Demonstrate the physical and chemical basis of heredity and variations through the
use of planar and three-dimensional models of genetic materials; and
3. Develop the students’ mastery of the basic concepts of genetics by accurately
demonstrating the different phases of cell division and the processes of DNA
replication, transcription and synthesis through the use teaching models (eg. gene
action kit).
Course Details:
The University LMS will be used for asynchronous learning and assessment. The link and class
code for LMS will be provided at the start of class through the class’ official Facebook
Messenger Group.
Edmodo
Google Classroom
University LMS
Major examinations will be given as scheduled. The scope and coverage of the examination
will be based on the lessons/topics as plotted in the course syllabus.
Module Overview
Introduction
This module provides students an introduction on the science of heredity. The topic
focus on the cytological basis of inheritance, Mendelian and non-Mendelian inheritance,
molecular structure of DNA, mutation and human genetics with focus to behavioral genetics.
This module also equips students with knowledge and skills in doing genetic crosses, that genes
come in pairs, alleles can be dominant or recessive, and how to use Punnet squares to predict
ratios of phenotypes in offspring. Mechanisms of DNA replication, RNA transcription and
protein translation and how gene expression can be regulated were also given emphasis on this
module.
Table of Contents
Genetics
Chapter 1
Introduction to Genetics
Chapter 1
Introduction to Genetics
Introduction
Genetics is a field of biology that studies how traits are passed from parents to their
offspring. The passing of traits from parents to offspring is known as heredity, therefore,
genetics is the study of heredity. These traits are described by the genetic information carried
by a molecule called DNA. The instructions for constructing and operating an organism are
contained in the organism's DNA. Every living thing on earth has DNA in its cells. A gene is
a hereditary unit consisting of DNA that occupies a spot on a chromosome and determines a
characteristic in an organism. Genes are passed on from parent to child and are believed by
many to be an important part of what decides looks and behavior.
This module will introduce you to the importance of understanding Genetics and how
it relates to you. This will provide information about the discovery and the progress that leads
to the development genetic and how it transformed the understanding scientific community
about heredity. It also covers the applications of genetics in agriculture, medicine and other
fields of sciences.
Specific Objectives
Duration
Lesson Proper
Genetics was coined by William Bateson from the Greek word gen, meaning to become
to grow into something.
Genetics is the branch of biology that deals with the principles of heredity and
variation in all living things. It is the core biological science that seeks to understand the
molecular and physical bases of biological diversity.
Beginnings of Genetics
Before Mendel’s time, heredity was thought to be a blending process and that offspring
were essentially mixture of different parental characteristics.
Birth Genetics
Publish his research result in 1866 but remained unrecognized by the scientific world
until 1900 (after his death).
Three scientist from Netherlands, Austria, and Germany rediscovered Mendel’s work.
The significance of his conclusions was recognized, other biologists immediately began
to conduct similar genetic studies on mice, chickens, and other organisms. The results
of these investigations showed that many traits indeed follow Mendel’s rules
The result of his experiments laid the foundation of the science of heredity.
1902, Bateson, Sanders, and Cuenot had provided the information indicating that
Mendel’s Principles also applied to animals.
Fruit fly experiments in Thomas Hunt Morgan’s Laboratory (1910) – his student
Sturtevent had an idea that genes are linearly arranged, next to each other, like pearls
on a necklace. Some genes are close to each other while the others are quite far from
one another.
Researches also try to find the physical place within the cell where heredity begins.
They started with chromosomes – slender strand of materials in the cell nucleus found
out that chromosome of a dividing cell were duplicated, with a copy being send to each
of the two new cells. Sturtevant realized that the chromosomes are likely to be the
physical place of the gene.
1927 – Herman Muller confirmed the idea that genes are located in the
chromosomes. Chromosomes of flies when damage by X-ray also affected the genes.
They found out that genes could be changed or altered.
1944 – monumental discovery when it was showed that genetic information are
contained in a chemical DNA (deoxyribonucleic acid) Avery, Macleod, and McCarty
transferred the DNA of a pneumonia-causing bacterium into a harmless kind,
transforming the letter into a deadly kind of bacterium.
1953 – James Watson and Francis Crick proposed the helical structure of the DNA
1960 – showed that there was a code made up of chemical adenine, thymine, cytosine,
and guanine in a special sequence within the DNA, the code was a triplet of the four
basic chemicals A, T, C, and G (ATC, AAA, AAC)
- Early human studies focused on easily observable characteristics such as urine color,
or the occurrence of serious diseases in a family.
- 1902 Archibald Garrod suggested that diseases were due to inborn errors of
metabolism, meaning that inheritance of defective genes results to the production of
defective enzymes leading to a disease. It is fairly evident that the same disease
clustered in a certain family.
- There about 500 specific gene defects that cause human disease have been identified.
But how many genes are there? Current estimates range from 70,000 to 150,000.
Human Genome Project, which was started in 1989, was organized to sequence the
entire human genome and to discover all human genes. Years of work are still needed
in order to reveal all the secrets of the human DNA.
2. Genetics in Agriculture
3. Legal Applications
4. Genetic Counseling
Suggested Readings
Additional Resources
Pierce, Benjamin A.2016. Essential of Genetics 3rd ed. New York: W. H. Freeman and
Company
Ramirez, D. A., Mendioro, M. S. and Laude, R. P. 2013. Lectures in Genetics 10th ed.
Laguna: University of the Philippines Los Banos.
Snustad, Peter D. & Simmons, Michael J. 2012. Principles of Genetics. 6th ed. John Wiley &
Sons, Inc.
Activity Sheet
ACTIVITY 1
Exercises
A. Matching Type: Match Column A with Column B by writing the letter of the correct
answer.
Column A Column B
In the early years of the twentieth century, why did many biologists and biochemists
believe that proteins were probably the genetic material?
LEVEL DESCRIPTION
Minimal effort.
Minimal grammar mechanics.
3 - Fair
Fair presentation.
Few supporting details
Somewhat unclear.
Shows little effort.
2 - Poor Poor grammar mechanics.
Confusing and choppy, incomplete sentences.
No organization of thoughts.
Assignment
In what particular portion of this learning packet, you feel that you are struggling or lost?
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To further improve this learning packet, what part do you think should be enhanced?
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NOTE: This is an essential part of course module. This must be submitted to the subject
teacher (within the 1st week of the class).