So, say I get a set of chromosomes from my Mum which contains the X chromosome and the same from my Dad, but with the Y chromosome. I now have two sets of the same 22 chromosomes, plus an X and a Y.
For chromosome number one for example, is everything from my Dad’s side activated? My Mum’s? Or is is a random selection of genes within each chromosome?
And does the X chromosome do anything for me, or is it turned off, and only used if I pass it on to the next generation?
Follow up question: I believe that women actually recombine their X chromosomes when passing these on, but men can’t recombine X and Y. So everything on your Dad’s side stays the same. Does this have any impact? For example are you more likely to inherit genetic defects from your Dad’s side?
You get half of your chromosomes from each of your parents, so their bodies are in charge of setting which half their child will use.
Afterwards which trait will be present goes into dominant and recessive genes.
(of course this is more complicated and someone might do a better job at explaining it in depth)
So, what: each individual sperm has half the father’s genes? Does each sperm have a different set, or are they all the same? What process in the father decides which genes make it into the half that goes into the sperm?
If the same process is happening in the egg, then same questions.
Yes, each sperm and egg are unique since the process they go through ensures the chromosomes have been mixed.
Both sex cells (gametes) go through meiosis.
shuffles the genes between the two chromosomes in each pair (one received from each parent), producing lots of recombinant chromosomes with unique genetic combinations in every gamete […] produces four genetically unique cells, each with half the number of chromosomes as in the parent
