Briefly discuss Mendel’s laws of Inheritance with suitable examples

Mendel's laws of inheritance are fundamental principles that describe the patterns of inheritance of genetic traits from parents to offspring. Gregor Mendel, an Austrian monk and botanist, discovered these laws in the 19th century after performing experiments with pea plants.

Law of Segregation: This law states that for each trait, an individual inherits two copies (alleles) from each parent, but only one copy is passed on to their offspring. The two alleles segregate during the formation of gametes, so each gamete receives only one allele.

Briefly discuss Mendel’s laws of Inheritance with suitable examples

For example, consider the trait of flower color in pea plants. The allele for purple flowers (P) is dominant over the allele for white flowers (p). If a pea plant with genotype Pp (heterozygous) is crossed with another Pp plant, the offspring will inherit one allele from each parent. The resulting Punnett square shows that 25% of the offspring will be homozygous dominant (PP), 50% will be heterozygous (Pp), and 25% will be homozygous recessive (pp).

For example, consider the traits of flower color and seed color in pea plants. The allele for yellow seeds (Y) is dominant over the allele for green seeds (y). If a pea plant with genotype PpYy (heterozygous for both traits) is crossed with another PpYy plant, the resulting Punnett square shows that there are four possible combinations of alleles in the offspring: PY, Py, pY, and py. Each combination has an equal chance of occurring because the alleles for each trait assort independently of each other.

In summary, Mendel's laws of inheritance provide a framework for understanding how genetic traits are passed down from parents to offspring. The law of segregation explains how alleles are separated during gamete formation, while the law of independent assortment explains how alleles for different traits are inherited independently of each other.

Eye Color: Eye color is an inherited trait that is determined by multiple genes. The gene for brown eyes (B) is dominant over the gene for blue eyes (b). If both parents have brown eyes, but each carries a recessive blue-eyed gene, they can still pass on the blue-eyed gene to their children. For example, if both parents are heterozygous for the brown-eyed gene (Bb), their children have a 25% chance of inheriting two recessive blue-eyed genes (bb) and having blue eyes.

mendel law of inheritance pdf; mendel's law of inheritance notes; mendel law of inheritance class 10; law of segregation; law of dominance; mendel's first law of inheritance; importance of mendel's law of inheritance; mendel's law of inheritance class 12 pdf

Blood Type: Blood type is determined by multiple alleles. There are four blood types: A, B, AB, and O. The A and B alleles are codominant, while the O allele is recessive. If one parent has blood type AB and the other has blood type O, their child could inherit either type A or B, or neither, depending on the combination of alleles inherited from each parent. For example, if the AB parent passes on the A allele and the O parent passes on the O allele, the child will have blood type A.

Cystic Fibrosis: Cystic Fibrosis is an inherited genetic disorder caused by a mutation in the CFTR gene. It is inherited in an autosomal recessive manner, meaning that a person must inherit two copies of the mutated gene (one from each parent) in order to develop the disorder. If both parents are carriers of the mutated gene, each child they have has a 25% chance of inheriting two copies of the mutated gene and developing the disorder.

 

For SOLVED PDF & Handwritten

WhatsApp No :- 7838475079

 

Huntington's Disease: Huntington's Disease is an inherited genetic disorder caused by a mutation in the HTT gene. It is inherited in an autosomal dominant manner, meaning that a person only needs to inherit one copy of the mutated gene from one parent in order to develop the disorder. If one parent has the disorder, each child they have has a 50% chance of inheriting the mutated gene and developing the disorder.

Post a Comment

Previous Post Next Post