PRINCIPLES OF INHERITANCE AND VARIATION

 

Sex determination in birds:

  • Female birds have two different sex chromosomes designated as Z and W.
  • Male birds have two similar sex chromosomes and called ZZ.
  • Such type of sex determination is called female heterogammety and male homogamety.

Sex determination in Honey bee:

  • Sex determination in honey bee based on the number of sets of chromosomes an individual receives.
  • An offspring formed from the fertilization of a sperm and an egg developed into either queen (female) or worker (female).
  • An unfertilized egg develops as a male (drone), by means of parthenogenesis.
  • The male have half the number of chromosome than that of female.
  • The female are diploid having 32 chromosomes and males are haploid i.e. having 16 numbers of chromosomes.
  • This is called haplodiploid sex determination system.
  • Male produce sperms by mitosis, they don not have father and thus cannot have sons, but have grandsons.

MUTATION:

  • Mutation is a phenomenon which results in alteration of DNA sequences and consequently results in changes in the genotype and phenotype of an organism.
  • In addition to recombination, mutation is another phenomenon that leads to variation in DNA.
  • Loss (deletion) or gain (insertion/duplication) of a segment of DNA results in alteration in chromosomes.
  • Since genes are located on the chromosome, alteration in chromosomes results in abnormalities or aberration.
  • Chromosomal aberrations are commonly observed in cancerous cells.
  • Mutations also arise due to change in a single base pair of DNA. This is known as point mutation. E.g. sickle cell anemia.
  • Deletion and insertions of base pairs of DNA causes frame shift mutations.

GENETIC DISORDERS:

Pedigree Analysis:

  • Analysis of traits in several of generations of a family is called the pedigree analysis.
  • In the pedigree analysis the inheritance of a particular trait is represented in the family tree over generations.

Autosomal Dominant:

  • Affected individuals have at least one affected parent
  • The phenotype generally appears every generation
  • Two unaffected parents only have unaffected offspring
  • Traits are controlled by dominant genes
  • Both males and females are equally affected
  • Traits do not skip generations
  • e.g. polydactyly, tongue rolling ability etc

Autosomal recessive:

  • Unaffected parents can have affected offspring
  • Traits controlled by recessive  genes and
  • Appear only when homozygous 
  • Both male and female equally affected
  • Traits may skip generations
  • 3:1 ratio between normal and affected. 
  • Appearance of affected children from normal parents (heterozygous)
  • All children of affected parents are also affected.
  • e.g.- Albinism, sickle cell anaemia etc

 

 

CBSE Biology (Chapter Wise) Class XII ( By Mr. Hare Krushna Giri )
Email Id : harekrushnagiri@yahoo.com



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