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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