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Y Chromosome Meaning
In therian mammals, such as humans and many other animals, the Y chromosome is one of the two sex chromosomes (allosomes). The X chromosome is the other. In several species, the presence or absence of the Y chromosome determines whether the offspring are born male or female, making it the sex-determining chromosome in these species.
Each cell in an individual typically contains one set of sex chromosomes. Males possess one X and one Y chromosome, whereas females possess two X chromosomes.
Y Chromosome Structure
The human Y chromosome is similar in size to chromosome 19 and has roughly 59 million base pairs of DNA. Only fathers and sons share the Y chromosome.
The SRY gene, found on the Y chromosome in mammals, causes male embryonic development. Other genes required for typical sperm production can also be found on the Y chromosomes of mammals and humans.
However, there are a few exceptions. In humans, some men have the “XXY” syndrome (two Xs and a Y), or the “XYY syndrome”(one X and two Ys), while some females have a single X instead of a double X or three Xs. Other exceptions occur when SRY is damaged (resulting in an XY female) or transferred to the X (resulting in an XX male).
Related Links:
- Homologous Chromosome – Structure and Functions
- Chromosomal Abnormalities in Humans
- Important Notes for NEET Biology – Chromosome Structure
Main Page: BYJU’S NEET
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