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CHROMOSOMAL THEORY OF INHERITANCE

This theory was proposed by Walter Sutton and Theodor Boveri (1902). Following are the main points of this theory

1. Gametes serve as the bridge between two successive generations.

2. Male and Female gametes play an equal role in contributing hereditary components of future generation.

3. Only the nucleus of sperm combines with ovum. Thus, the hereditary information is contained in the nucleus.

4. Chromatin in the nucleus is associated with the cell division in the form of chromosomes.

5. Any type of deletion or addition in the chromosomes can cause structural and functional changes in living beings.

6. A sort of parallelism is observed between Mendelian factors and chromosomes.

7. A number of genes or Mendelian factors are found in each chromosome.

8. Determination of sex in most of the animals and plants is affected by specific chromosomes. These chromosomes are called sex chromosomes.

Parallelism Between Gene and Chromosomes 

1. Chromosomes are also transferred from one generation to the next as in the case of genes (Mendelian factors).

2. The number of chromosomes is fixed in each living species.These are found as homologous pairs in diploid cells. One chromosome from father and the other contributed by the mother constitute a homologous pair.

3. Before cell division, each chromosome as a whole and the alleles of genes get replicated and are separated during mitotic division.

4. Meiosis takes place during gamete formation. Homologous chromosomes form synapses during prophase-I stage which in later course get separated and transferred to daughter cells. Each gamete or a haploid cell has only one allele of each gene present in the chromosome.

5. A characteristic diploid number is again established by the union of the two haploid gametes.

6. Both chromosomes and the alleles (Mendelian factors) behave in accordance to Mendel's law of segregation.

Inheritance of Two Genes: Chromosomal Theory | Additional Study Material for NEETIn the homologus chromosomes of a pure tall plant, allele (T) is found for tallness in each chromosome. Likewise, in a pure dwarf plant (tt), allele (t) is present in each chromosome.

These homologous chromosomes get separated during meiotic division. Hence, each gamete possesses only one chromosome of an each pair. Accordingly, all the gametes of tall plants possess a chromosome with an allele of tallness (T), while the gametes of dwarf plants possess a chromosome with an allele for dwarfness (t). Their cross to produce F1 generation will yield tall hybrid plants with homologous chromosomal pair containing Tt allelic pair. In this generation two kinds of gamete will be formed during gameto -genesis, 50% with the allele (T) for tallness and 50% with the allele for dwarfness (t).Random combination of these gametes will produce offsprings in F2 generation in the ratio of 25% pure tall (TT), 50% hybrid tall (Tt) and 25% dwarf (tt)

Inheritance of Two Genes: Chromosomal Theory | Additional Study Material for NEET

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FAQs on Inheritance of Two Genes: Chromosomal Theory - Additional Study Material for NEET

1. What is the chromosomal theory of inheritance?
Ans. The chromosomal theory of inheritance states that genes are located on chromosomes and that the inheritance of traits is determined by the transmission of chromosomes from parents to offspring during reproduction. This theory was proposed by Thomas Hunt Morgan and his colleagues in the early 20th century based on their experiments with fruit flies.
2. How does the chromosomal theory explain the inheritance of two genes?
Ans. According to the chromosomal theory, each gene is located at a specific position on a chromosome called a locus. When two genes are located on the same chromosome, they tend to be inherited together, a phenomenon known as genetic linkage. The closer the genes are to each other on the chromosome, the less likely they are to be separated during the process of genetic recombination.
3. Can genes located on different chromosomes be inherited together?
Ans. Genes located on different chromosomes are not usually inherited together. This is because during the process of genetic recombination, which occurs during meiosis, chromosomes independently assort and separate from each other. This process leads to the shuffling of genetic material and the independent inheritance of genes located on different chromosomes.
4. How can the chromosomal theory be applied in genetic counseling?
Ans. The chromosomal theory of inheritance provides a foundation for understanding the transmission of genetic traits and diseases. Genetic counseling uses this knowledge to assess the risk of inheriting certain conditions based on the presence or absence of specific genes or chromosomal abnormalities. It helps individuals and families make informed decisions about reproductive options and understand the probability of passing on genetic disorders.
5. Can the chromosomal theory explain all patterns of inheritance?
Ans. While the chromosomal theory of inheritance provides a fundamental framework for understanding genetic inheritance, it does not explain all patterns of inheritance. Some traits, such as those influenced by multiple genes or environmental factors, may not follow simple Mendelian inheritance patterns. Additionally, certain genetic disorders may be caused by mutations in genes located outside the chromosomes, such as in mitochondrial DNA.
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