attention in biology for the next century. The entire body of
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4.1 Mendel's Laws of Inheritance
Explanation4.1 Mendel's Laws of Inheritance
Genetics is the branch of biology that studies inheritance and variation of characters from parents to offspring. Gregor Mendel, through his pioneering hybridisation experiments on garden pea plants from 1856 to 1863, established the foundational principles of inheritance. Mendel's approach was unique because he applied statistical analysis and mathematical logic to biological problems, using a large sample size to ensure reliability and reproducibility of results across generations. He studied seven pairs of contrasting traits in pea plants, such as tall vs dwarf plants and yellow vs green seeds, which allowed him to formulate general rules of inheritance. Mendel used true-breeding pea lines, which consistently produced the same trait over generations, to perform controlled crosses. His work demonstrated that traits are inherited as discrete units, later called genes, which occur in pairs known as alleles. Mendel's experiments revealed that in a cross between two contrasting traits, the F1 generation expressed only one trait (dominant), while the other (recessive) reappeared in the F2 generation in a 3:1 ratio. This led to the formulation of Mendel's Laws of Inheritance, which explain how traits are transmitted and expressed without blending. These laws laid the groundwork for modern genetics and explained the predictable patterns of inheritance observed in living organisms.
- Mendel studied inheritance using garden pea plants with contrasting traits.
- He applied statistical methods to biological inheritance.
- True-breeding lines ensured stable trait inheritance.
- Traits are controlled by discrete units called factors (genes).
- F1 generation shows dominant trait; recessive trait reappears in F2 in 3:1 ratio.
- Mendel's work established the laws of inheritance.
- 📌 Genetics: Study of inheritance and variation of traits.
- 📌 True-breeding: Organisms that produce offspring with the same trait over generations.
- 📌 Gene: Unit of inheritance controlling a trait.
4.2 Inheritance of One Gene
Explanation4.2 Inheritance of One Gene
Mendel's monohybrid cross experiments focused on inheritance of a single gene controlling a trait, such as plant height. Crossing true-breeding tall (TT) and dwarf (tt) pea plants produced F1 progeny that were all tall (Tt), demonstrating dominance of the tall allele. Self-pollination of F1 plants yielded an F2 generation with a phenotypic ratio of approximately 3 tall : 1 dwarf, and a genotypic ratio of 1 TT : 2 Tt : 1 tt. This showed that alleles segregate during gamete formation, with each gamete receiving only one allele (Law of Segregation). Dominant alleles mask the expression of recessive alleles in heterozygotes (Law of Dominance). Mendel used capital letters for dominant alleles and lowercase for recessive alleles. The Punnett square is a graphical tool to predict genotypic and phenotypic ratios in offspring. Test crosses, where an organism with dominant phenotype but unknown genotype is crossed with a homozygous recessive individual, help determine the unknown genotype based on progeny ratios. Variations to simple dominance include incomplete dominance, where heterozygotes show intermediate phenotype (e.g., pink flowers in snapdragon), and co-dominance, where both alleles express equally (e.g., ABO blood groups). These concepts explain the diversity of inheritance patterns beyond Mendel's original laws.
- Monohybrid cross studies inheritance of a single gene.
- Dominant allele expresses in heterozygotes; recessive allele is masked.
- Alleles segregate during gamete formation (Law of Segregation).
- F2 generation shows 3:1 phenotypic ratio and 1:2:1 genotypic ratio.
- Punnett square predicts offspring genotypes and phenotypes.
- Test cross determines genotype of dominant phenotype individual.
- 📌 Monohybrid cross: Cross involving one gene with two alleles.
- 📌 Dominant allele: Allele expressed in heterozygous condition.
- 📌 Recessive allele: Allele masked in heterozygous condition.
4.2.2.1 Incomplete Dominance
Concept4.2.2.1 Incomplete Dominance
Incomplete dominance occurs when the heterozygous phenotype is intermediate between the two homozygous phenotypes, rather than one allele being completely dominant over the other. A classic example is flower colour in snapdragon (Antirrhinum sp.). Cr
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Q1.1. Mention the advantages of selecting pea plant for experiment by Mendel.
Answer:
Mendel selected pea plants for his experiments because they have several advantages: - Pea plants have easily distinguishable traits (such as flower color, seed shape). - They have a short life cycle, allowing multiple generations in a short time. - Pea plants can self-pollinate as well as cross-pollinate, enabling controlled breeding. - They produce a large number of offspring, providing sufficient data for statistical analysis. - The traits studied are inherited in a clear dominant-recessive pattern, simplifying analysis.
Explanation:
These advantages allowed Mendel to observe clear patterns of inheritance and formulate his laws of genetics.
Q2.2. Differentiate between the following - (a) Dominance and Recessive (b) Homozygous and Heterozygous (c) Monohybrid and Dihybrid.
Answer:
(a) Dominance and Recessive: - Dominance: The allele that expresses its trait even when present in a single copy (heterozygous condition). - Recessive: The allele whose trait is masked in the presence of a dominant allele and only expressed when homozygous. (b) Homozygous and Heterozygous: - Homozygous: An organism having two identical alleles for a particular gene (e.g., AA or aa). - Heterozygous: An organism having two different alleles for a particular gene (e.g., Aa). (c) Monohybrid and Dihybrid: - Monohybrid: A cross involving a single pair of contrasting traits (one gene locus). - Dihybrid: A cross involving two pairs of contrasting traits (two gene loci).
Explanation:
These distinctions are fundamental to understanding inheritance patterns and genetic crosses.
Q3.3. A diploid organism is heterozygous for 4 loci, how many types of gametes can be produced?
Answer:
If an organism is heterozygous for 4 loci, each locus has two different alleles. The number of types of gametes produced = 2^n, where n = number of heterozygous loci. Here, n = 4. Therefore, number of gametes = 2^4 = 16. Hence, 16 types of gametes can be produced.
Explanation:
Each heterozygous locus can produce two types of alleles, and the gametes receive one allele from each locus independently, so total combinations are 2^4 = 16.
Q4.4. Explain the Law of Dominance using a monohybrid cross.
Answer:
Law of Dominance states that when two contrasting traits are crossed, only one trait (dominant) is expressed in the F1 generation, while the other (recessive) remains hidden. Using a monohybrid cross of pea plants: - Cross pure tall (TT) with pure dwarf (tt). - F1 generation: All plants are tall (Tt) because tall (T) is dominant. - F2 generation (Tt x Tt): Phenotypic ratio is 3 tall : 1 dwarf. This shows that the dominant trait masks the recessive trait in heterozygous condition.
Explanation:
The monohybrid cross demonstrates that dominant alleles express their trait over recessive alleles in heterozygotes, confirming the Law of Dominance.
Q5.5. Define and design a test-cross.
Answer:
Test-cross is a cross between an individual showing the dominant phenotype (but unknown genotype) and a homozygous recessive individual. Purpose: To determine the genotype of the dominant phenotype individual. Design: - Cross the individual with dominant phenotype (genotype could be homozygous dominant or heterozygous) with a homozygous recessive individual. - Analyze the offspring: - If any offspring show recessive phenotype, the tested individual is heterozygous. - If all offspring show dominant phenotype, the tested individual is homozygous dominant.
Explanation:
Test-cross helps in identifying the genotype of an organism showing dominant phenotype by crossing it with a homozygous recessive individual and observing the phenotypes of progeny.
Q6.6. Using a Punnett Square, workout the distribution of phenotypic features in the first filial generation after a cross between a homozygous female and a heterozygous male for a single locus.
Answer:
Let the gene locus have alleles A (dominant) and a (recessive). Female genotype: AA (homozygous dominant) Male genotype: Aa (heterozygous) Punnett Square: A a A | AA Aa A | AA Aa Genotypes of offspring: - 50% AA - 50% Aa Phenotypes: - Both AA and Aa show dominant phenotype. - Therefore, 100% offspring show dominant phenotype.
Explanation:
Crossing homozygous dominant female with heterozygous male results in all offspring showing dominant phenotype, with genotypes split equally between homozygous dominant and heterozygous.
Q7.7. When a cross in made between tall plant with yellow seeds (TtYy) and tall plant with green seed (Ttyy), what proportions of phenotype in the offspring could be expected to be (a) tall and green. (b) dwarf and green.
Answer:
Given: Parent 1 genotype: TtYy (tall, yellow seeds) Parent 2 genotype: Ttyy (tall, green seeds) Genes: T = tall (dominant), t = dwarf (recessive) Y = yellow seeds (dominant), y = green seeds (recessive) Step 1: Determine gametes Parent 1 (TtYy) gametes: TY, Ty, tY, ty Parent 2 (Ttyy) gametes: Ty, ty Step 2: Make Punnett square with 4 x 2 = 8 combinations Offspring genotypes and phenotypes: 1) TY x Ty = TTYY (tall, yellow) 2) TY x ty = TTYy (tall, yellow) 3) Ty x Ty = TTYy (tall, yellow) 4) Ty x ty = TTyy (tall, green) 5) tY x Ty = TtYY (tall, yellow) 6) tY x ty = TtYy (tall, yellow) 7) ty x Ty = TtYy (tall, yellow) 8) ty x ty = Ttyy (tall, green) Note: All offspring have at least one T allele, so all are tall. But question asks for dwarf and green (dwarf = tt), so no dwarf offspring expected. Phenotype proportions: (a) Tall and green: TTyy and Ttyy genotypes From above, TTyy (1/8), Ttyy (1/8) = 2/8 = 1/4 (b) Dwarf and green: tt yy genotype No tt genotype in offspring, so 0. Answer: (a) Tall and green = 1/4 (b) Dwarf and green = 0
Explanation:
By determining gametes and crossing them, we find all offspring have at least one dominant T allele (tall), so no dwarf offspring. Green seed phenotype requires yy genotype, which occurs in 1/4 of offspring.
Q8.8. Two heterozygous parents are crossed. If the two loci are linked what would be the distribution of phenotypic features in $[1mF_1[0m$ generation for a dihybrid cross?
Answer:
When two loci are linked, the genes are located close together on the same chromosome and tend to be inherited together. Given: Both parents heterozygous for two loci (e.g., AaBb x AaBb), but loci are linked. In linked genes, the expected phenotypic ratio deviates from the classic 9:3:3:1 ratio of independent assortment. The phenotypic distribution depends on the recombination frequency: - If no crossing over, only parental combinations appear. - If crossing over occurs, recombinant phenotypes appear but less frequent. Therefore, the F1 generation will have more parental type phenotypes and fewer recombinant phenotypes. Exact distribution depends on recombination frequency, but the key point is linked genes do not assort independently, altering phenotypic ratios.
Explanation:
Linked genes violate Mendel's law of independent assortment, leading to phenotypic ratios skewed towards parental types in F1 generation.
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Biology · Class 12