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Transmission Genetics: Concepts and Principles

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Transmission genetics is the transmission of genetic information from one generation to the next or from one part of a cell to another. Read the article to know more.

Written by

Hemamalini. R

Medically reviewed by

Dr. Arpit Varshney

Published At March 1, 2023
Reviewed AtDecember 29, 2023

Introduction

Genetic transmission is the driving force behind evolution. Therefore, the fundamental laws of inheritance are essential for understanding disease transmission patterns. The inheritance patterns of single-gene disorders are referred to as Mendelian since Gregor Mendel was the first to notice the various patterns of gene segregation for particular traits in garden peas and was able to calculate the likelihood of a trait recurring in later generations. A complete family history will be necessary to determine a pattern of transmission if a family is affected by a disease. Family history might also aid in ruling out hereditary diseases, particularly for prevalent diseases when environment and behavior are major contributors.

What Are Transmission Genetics?

Transmission genetics is a branch of genetics dealing with the study of inheritance in people. It is the transmission of genetic information from one generation to the next (from parents to children) or from one part of a cell to another, nearly identical to heredity. It is otherwise known as classical genetics. In transmission genetics, cross-sexual reproduction occurs between individuals, and the development of traits in children is studied. The basis of classical or transmission genetics is Gregor Mendel's analysis of the hereditary behavior of seven genes.

What Is the Focus of Transmission Genetics?

Transmission genetics is the field of genetics that studies the processes involved in transferring genes from parents to their offspring. Cell division, cell cycle, reproduction, replication, transcription, and signal transduction are some of the fundamental biological processes examined under it. The basis of classical or transmission genetics is cell division, including chromosomes, which comprise inheritance-containing units called genes. Mitosis is the division of somatic cells that contain 46 chromosomes (22 pairs of autosomes and two sex chromosomes, either XX or YY). A single somatic cell undergoes mitosis, resulting in two daughter cells, each having two diploid chromosomes (46). Only germ cells undergo meiosis, producing two gametes, each with a haploid number of chromosomes (23).

What Is Mendel's Concept of a Gene?

Gregor Mendel is the father of genetics. He was the first to demonstrate the inheritance pattern of traits from one generation to the next. In 1866, he developed the fundamental laws of genetics based on his research on the trait inheritance in the garden pea, Pisum sativum. Mendel started with pure-bred pea plants because they consistently produced offspring with the same trait as the parent plant. Then, he cross-bred pea plants to discover the inheritance pattern over many generations.

He followed the inheritance of the seven characteristics of the pea plant, including:

  • Pea color (green or yellow).

  • Pea shape (wrinkled or round).

  • Plant height (short or tall).

  • Flower color (white or purple).

  • Flower position (axial or terminal).

  • Pod color (green or yellow).

  • Pod shape (constricted or inflated).

Mendel's experiments would not have been successful unless he had chosen traits that were entirely dominant or recessive (contrasting traits) or traits that were all found on distinct chromosomes (pea plants have seven chromosomes). Some basics of Mendel's genetics include the following:

  • Alleles refer to each gene's two different forms.

  • An organism is said to be homozygous if it has two copies of the same allele.

  • An organism is said to be heterozygous if it has various alleles of the same gene.

  • If an allele is dominant, it is expressed anytime that allele is present.

  • Recessive traits are those that are hidden by one another.

  • A recessive allele is covered or hidden by a dominant allele.

  • The genotype is all an individual's genetic information about a specific trait. In a diploid organism, this indicates two copies.

  • The phenotype of an individual comprises those features that are manifested and may be observed (physical traits) or measured (chemical characteristics). A heterozygous individual for quality might only exhibit the effects of one allele (a dominant one) and not the other recessive one.

  • Cross-breeding or crossing is the process of combining two genetically distinct species.

  • Hybrids are the offspring of such crosses.

  • The P or paternal generation refers to the parents.

  • The F1 generation refers to the children of these parents (first filial).

Why Did Mendel Select the Pea Plant for His Experiment?

Mendel chooses Pisum sativa (pea plant) as it has the following characteristics:

  • There are many variants with contrasting traits.

  • True-breeding, self-pollinating varieties.

  • It is simple to cut portions to cross-pollinate.

  • Requires little space.

  • Produces many offspring.

What Are the Principles of Inheritance?

Two principles behind inheritance include the following:

1. Principle of Unit Factors: In every organism, single factors cause their features. It is called unit factors. Mendel did not know how these attributes were passed down, and now Mendel's unit factors are called genes.

2. Principle of Dominance: In an organism, some traits are visible or pronounced, and some are hidden, i.e., dominant and recessive.

  • Dominant Genes - Dominant Genes are called functional alleles. Functional genes or dominant genes are written in uppercase letters.

    • Melanin gene M.

    • Pepsin gene P.

    • Free earlobe gene = F.

    • Polydactyly = P.

  • Recessive Genes - Recessive genes are called non-functional alleles. This non-functional or dysfunctional gene is written in lowercase letters.

    • mutated melanin gene = m.

    • mutated free ear lobe gene = f.

    • nonfunctional polydactyly gene = p.

  • Recessive traits are those that are hidden by one another. When an allele has two copies and no other alleles, it is said to be homozygous, and only then does it manifest itself. A recessive allele is covered or hidden by a dominant allele.

  • Dominance - Functional genes are responsible for dominant conditions. The trait can be caused by a single copy of the gene called polydactyly Pp. Examples: Rolling of the tongue, hitchhiker's thumb.

  • Incomplete Dominance - Dominance does not occur in some allele combinations. Instead, the two features are expressed equally. For instance, the color dominance of snapdragon blossoms needs to be completed.

  • Codominance or Multiple Alleles - Genes can mutate or alter. There may be various DNA sequences for a trait. When a gene exhibits co-dominance, all its variants are active and equally responsible for the phenotype. It is also referred to as multiple alleles. AB antigen type and sickle cell trait (Hbs) are two examples.

  • Polygenic Inheritance - Although alleles influence many traits at a single location on the chromosome, some features are influenced by the interaction of genes on several chromosomes or at different locations on a single chromosome. The Inheritance of this condition is polygenic.

  • Sex-Linked Traits - Genes on the X or Y chromatin are responsible for sex-related characteristics. Genes on the X or Y chromatin strands might be dominant or recessive. The likelihood of having a sex-related attribute depends on the person's gender. Examples include hemophilia A and red-green colorblindness.

What Are the Results of Mendel's Experiments?

Mendel tested inheritance patterns through breeding experiments in the garden of his monastery. Over numerous generations, he crossed common pea plants (Pisum sativum) with specified features. After crossing two plants that differed in a single feature, Mendel found that the first generation, or F1, was exclusively composed of individuals expressing one of the traits (short stems vs. tall stems, round vs. wrinkled peas, purple flowers vs. white flowers, etc.). However, when this generation was crossed, its children, the F2 (second filial generation), displayed a 3:1 ratio, meaning that three offspring shared one parent's trait and one offspring shared the characteristic of the other parent.

Mendel then proposed that genes can be composed of three pairs of hereditary units, which he referred to as factors: AA, Aa, and aa. The large A stands for the dominant factor, whereas the small A stands for the recessive factor. In Mendel's crosses, the F1 generation was Aa, the F2 generation was AA, Aa, or aa, and the starting plants were homozygous AA or aa. The relationship between these two determines the physical trait.

What Are Mendel's Laws of Inheritance?

The following three principles, or laws, summarize Mendel's observations and conclusions.

Law of Dominance - Mendel's law of dominance states that when two organisms with different traits combine, each offspring only demonstrates the characteristic of one parent. A person will develop the dominant feature if the dominant factor is present. If both elements are recessive, the recessive trait will only manifest.

Law of Segregation - According to the law of segregation, although the alleles of a character remain together for a long time, they do not mix and separate during gametogenesis, so each gamete acquires just one allele of a trait, which is either dominant or recessive. When homozygous tall and dwarf pea plants from the F1 generation self-fertilize, tall and dwarf plants are produced in a 3:1 ratio.

Law of Independent Assortment - According to the law of independent assortment, when more than two characters are taken, a character's alleles can go through any combination to produce a phenotype distinct from both parents.

What Are the Exceptions to Mendel's Law?

Some exceptions to Mendel's rules or laws have been identified as our understanding of genes, and heredity has grown. For example, the independent assortment principle is not applicable if the genes are close to one another (or connected) on a chromosome. Moreover, alleles may not necessarily interact in a typical recessive or dominant manner, especially if they are codominant or differ in penetrance or expressivity.

Conclusion

Transmission genetics, often known as classical genetics, studies the transmission of genes from parents to children. Mendel's research has provided scientists with the foundation for mathematically forecasting the chances of genotypes and phenotypes in the offspring of a genetic cross. On the other hand, not all genetic observations can be predicted and explained using Mendelian genetics. The concepts of Inheritance and the understanding of unit inheritance were the basis of our modern science of genetics.

Frequently Asked Questions

1.

How Does Transmission Genetics Differ from Molecular Genetics?

Transmission genetics focuses on how traits are passed from generation to generation through the study of inheritance patterns and Mendelian principles. It primarily explores the observable characteristics and their predictable transmission patterns within populations. On the other hand, molecular genetics delves into the mechanisms underlying heredity, investigating the role of genes, DNA, and genetic information at the molecular level. While transmission genetics emphasizes inheritance patterns, molecular genetics delves into the genetic material and its interactions.

2.

Who Is Credited with the Discovery of Transmission Genetics?

The discovery of transmission genetics is credited to Gregor Mendel, an Austrian scientist and Augustinian friar, who conducted groundbreaking experiments with pea plants in the mid-19th century. Mendel's meticulous observations and systematic breeding experiments unveiled the principles of inheritance and laid the foundation for our understanding of genetic traits being passed from generation to generation. His work became the basis for modern genetics and revolutionized our knowledge of heredity.

3.

What Are the Various Forms of Genetic Inheritance?

Various forms of genetic inheritance include autosomal dominant, autosomal recessive, X-linked dominant, X-linked recessive, and mitochondrial inheritance. Autosomal dominant traits are expressed when a single gene copy is present, while autosomal recessive traits require two copies for expression. X-linked traits are carried on the X chromosome and can be dominant or recessive. Mitochondrial inheritance involves genes located in the mitochondria and is typically passed from mother to offspring. Each form of inheritance follows specific patterns that dictate how genetic traits are transmitted within families.

4.

Is Transmission Genetics Considered a Subdivision of Genetics?

Yes, transmission genetics is indeed considered a subdivision of genetics. It specifically focuses on the study of how genetic traits are passed from parents to offspring through generations. By examining inheritance patterns and understanding the principles of genetic transmission, this field contributes significantly to understanding how traits are inherited, expressed, and distributed within populations.

5.

What Categorizations Exist Within the Field of Genetics?

The field of genetics encompasses several distinct categorizations. These include transmission genetics, which investigates the inheritance of traits between generations; molecular genetics, which delves into the molecular mechanisms underlying genetic information and gene expression; population genetics, which examines how genetic traits change within populations over time; and evolutionary genetics, which explores how genetic variation contributes to the evolution of species. Each category offers unique insights into heredity, inheritance, and genetic diversity.

6.

What Fundamental Concept Underlies Transmission Genetics?

The fundamental concept underlying transmission genetics is the study of how genetic traits are passed from parents to offspring. It involves exploring patterns of inheritance, understanding the role of genes, and deciphering the mechanisms by which traits are transferred across generations. This concept forms the basis for understanding the hereditary factors that shape the characteristics of individuals and populations, contributing to our knowledge of genetic diversity and how traits are propagated through successive generations.

7.

Enumerate Two Mechanisms of Genetic Transfer?

Two mechanisms of genetic transfer are known as meiosis and mitosis. Meiosis is the specialized cell division process that produces gametes (sperm and egg cells) with half the usual number of chromosomes, contributing to genetic diversity. Mitosis, on the other hand, is responsible for cell replication and growth, ensuring that genetic information is accurately transmitted to daughter cells. These mechanisms play crucial roles in the transmission of genetic material during reproduction and growth, allowing for the inheritance of traits and the maintenance of genetic stability.

8.

What Is the Significance of Genetic Transmission?

The significance of genetic transmission lies in its role in passing on hereditary information from one generation to the next. This process ensures the continuity of genetic traits and characteristics within a species. Understanding genetic transmission is essential for comprehending inheritance patterns, predicting the likelihood of traits in offspring, diagnosing genetic disorders, and advancing fields such as medicine, agriculture, and evolutionary biology. By studying genetic transmission, scientists can gain insights into the mechanisms that shape biological diversity and contribute to the overall understanding of life's intricacies.

9.

How Are Patterns of Transmission Determined?

Patterns of genetic transmission are determined by the inheritance principles established by Gregor Mendel, which include segregation and independent assortment. Segregation refers to the separation of alleles during gamete formation, ensuring that each offspring inherits one allele from each parent. Independent assortment involves the random distribution of gene pairs into gametes, generating diverse genetic combinations. These principles govern how genetic traits are passed down and contribute to the variability observed in offspring, playing a fundamental role in shaping the genetic makeup of future generations.

10.

How Do Genes Get Passed from One Generation to the Next?

Genes are passed from one generation to the next through genetic inheritance. Parents transmit their genetic material, including genes, to their offspring during reproduction. This transfer occurs through gametes (sperm and egg cells), which combine during fertilization to create a new individual with a unique combination of genetic traits inherited from both parents. This mechanism ensures the continuity of species and the passing on of genetic information that determines an individual's traits, characteristics, and potential health outcomes.

11.

What Methods Are Used to Analyze Gene Transmission?

Gene transmission is analyzed through various techniques and methodologies in genetics. These include pedigree analysis, where family trees are constructed to track the inheritance of specific traits; molecular techniques like polymerase chain reaction (PCR) to amplify and study specific DNA sequences; and genome sequencing to decode an individual's genetic makeup. These methods provide insights into gene transmission patterns, inheritance probabilities, and the identification of genetic mutations or variations that contribute to traits and diseases. Analyzing gene transmission is essential for understanding genetic diversity, hereditary disorders, and the complex interplay between genes and their transmission across generations.

12.

How Does DNA Facilitate the Conveyance of Genetic Data to Offspring?

DNA facilitates the conveyance of genetic information to offspring through DNA replication and cell division. During reproduction, parent cells undergo meiosis, a specialized cell division that produces gametes with half the genetic material. Fertilization combines the gametes to restore the full complement of DNA in the offspring. The genetic information encoded in DNA sequences determines the traits and characteristics of the offspring, ensuring the inheritance of traits from parents to their progeny. This fundamental process is integral to the perpetuation of species and the preservation of genetic diversity.

13.

What Does Transmission Genetics Signify?

In biology, transmission genetics refers to the study of how genetic traits are inherited and passed from one generation to the next. It focuses on understanding inheritance patterns, the principles governing genetic transfer, and the mechanisms by which traits are propagated within populations. This branch of genetics provides insights into the diversity of life, the variation in traits among individuals, and how genetic information shapes the characteristics of organisms over successive generations.

14.

Which Type of Genetic Recombination Employs Viruses for Gene Transfer?

The type of genetic recombination that relies on viruses to transfer genes is known as transduction. In this process, viruses called bacteriophages (phages) carry bacterial DNA from one bacterium to another. During infection, phages can accidentally package bacterial DNA and transfer it to a recipient bacterium, leading to genetic recombination. Transduction plays a crucial role in bacterial evolution and the exchange of genetic material between different bacterial strains, contributing to genetic diversity and adaptation.

15.

Which Branch of Genetics Is Concerned with the Passage of Hereditary Traits Across Generations?

The branch of genetics concerned with the passage of hereditary traits across generations is called transmission genetics. This field explores the patterns of inheritance, the mechanisms of genetic transfer, and the factors influencing the transmission of traits from parents to offspring. It delves into the principles that govern genetic inheritance and how traits are passed down within populations over time, forming a foundational aspect of our understanding of genetics and heredity.

16.

What Accounts for the Differing Rates of Gene Transfer?

Differing rates of gene transfer can be attributed to several factors, including the type of genetic material being transferred, the mechanisms of transfer involved, and the environmental conditions. Some genes may have higher transfer rates due to their location on mobile genetic elements like plasmids or transposons. Environmental factors such as stress or selective pressures can also influence the frequency of gene transfer events. Additionally, specific molecular mechanisms, such as conjugation, transformation, or transduction, can impact gene transfer efficiency between organisms.
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Dr. Arpit Varshney
Dr. Arpit Varshney

General Medicine

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