In man it has been found that Y-chromosomes are genetically inert in comparison to the X-chromosomes and other chromosomes and only a few genes are present in the human Y-chromosome.
As per the chromosomal make-up of human male and female, females contain a higher dose of functional gene containing chromosome than males (Female chromosome numbers = 44 + XX and Male chromosome number = 44 + XY).
The geneticists have observed that in some cases, female homozygous for the genes in the X-chromosomes do not express a trait more markedly than do hemizygous males.
So, it must be a mechanism of “dosage compensation”, through which the effective dosage of genes of the two sexes is made equal or nearly so.
This mechanism of compensating the differential doses of functional sex chromosomes in male and female human is effected by the inactivation of one X-chromosome in the normal female.
The genetically inactive X- chromosome or condensed X-chromosome is called heterochromatin or sex-chromatin body or Barr body.
Of the two X-chromosomes in females, which X-chromosome becomes inactive is a matter of chance, but it should be remembered that once an X- chromosome has become inactivated, all cells arising from that cell will keep the same inactive X-chromosome.
The inactive-X hypothesis or the Lyon’s hypothesis or the Dosage Compensation is widely known from 1961 which states that only one of the two X chromosomes in the homogametic sex is functional while the other condenses and is inactivated.
The X inactivated in some cells would be that from the father, in other cells it would be that from the mother.
Hence any tissue in the body of a woman would be a mosaic of cells which would show dominance of all genes having diffusible products.