I have taken this bait.
Please enjoy this wall of text! Prepared with love....every cell in the human body is designated an x or a y trust me there’s no discussing this...
...every single cell in your body is made up of 22 or so chromosomes...
With the exception of germline cells (sperm and mature eggs), most cells are diploid, and will have two copies of each chromosome; a set of 23 derived from the egg, and a set derived from the sperm. In most humans* this is a total of 46 different chromosomes. As previously stated, this is a set from both parents; as a result, cells from a genetically male human will have
both X and Y chromosomes present, whereas cells from a genetically female human will have
two X chromsomes** present.
Germline cells (sperm and egg cells) are haploid, and will have a total of 23 chromosomes (as a result of meiosis) [with exceptions causing *]; this includes either X or Y (in sperm), or one copy of X (in eggs). These are the only cells which could be considered "designated X or Y".
Some cells (red blood cells and platelets***) are enucleated, meaning they have no chromosomes at all. (Red blood cells yeet their nucleus during their development, to save space; they stop transcribing their DNA, and downregulate translation/protein synthesis).
Notably, none of these numbers is 22.
Organ donation between sex works simply because each cell is designated x or y not because it is and doesn’t work...
to be honest, I'm not even entirely sure what this sentence is saying.
The basis of organ transplant rejection is attack by the recipient's immune system towards donor cells, in response to foreign antigen presented on cell surfaces.
Hyperacute rejection commonly happens as a result of blood type mismatch; blood vessel walls are attacked by recipient antibody; the same mechanism as the "acute haemolytic transfusion reaction" you'll get from wrong-bloodbagging.
Acute rejection occurs due to recognition of MHC (the major histocompatibility complex, used for presenting antigen to immune cells) as foreign. MHC is coded for on
chromosome 6, with the major part needing to be matched being the HLA loci. Sibling transplants are more commonly accepted because closely shared ancestry means HLA haplotypes are more likely to match up, reducing the chance that they're seen as "foreign".
Presence or absence of an X or Y chromosome has little bearing on transplant rejection. This is because, as mentioned, MHC is coded for on chromosome 6. However, as there are some non-identical genes between X and Y, dead cells in tranplants may contain peptides from Y-chromosome transcripts which induce an indirect immune response within the transplant, generally in organs from a genetically male donor into a genetically female recipient.
...sry genome is responsible for making an x from a y so the x autosme is just a modified x...
The SRY gene is largely responsible for driving initial sex determination, but SRY is not the only difference between X and Y chromosomes. The Y chromosome is mostly gene-deficient compared to X - this is evidenced by sex-linked disorders (since males have no "backup copy" of X, a recessive X mutation will always be expressed in males - red-green colourblindness is an often-given example), as well as "X-only" aneuploidy being non-lethal, whereas "Y-only" aneuploidy is (see *). In addition, Y has paralogues of some genes on X - structurally similar but non-identical proteins.
Also, the sex chromosomes are not autosomes. please don't call them autosomes.
please read real scientific papers and not some random angry leftists view from YouTube
Source:
dude just trust me i'm a second-year undergraduate studying biochem and pathology at cambs rn
Some of my lecturers might be angry youtube leftists, but they're all qualified academics (as far as the uni knows)
Go wash your hands all that cheese dust starting to effect the way you think
no. i will inhale the cheese dust and you cannot stop me. it gives me super brain powers.
god I love footnotes:
* Aneuploidy (abnormality in the number of chromosomes) exists; Down syndrome is a prime example, where there are three copies of chromosome 21 present (for a total of 47); other trisomies on autosomes (the non-sex chromosomes) are usually fatal, though some others are survivable. Aneuploidy of sex chromosomes is generally non-fatal unless there is altogether no X chromosome; there have been recorded rare cases of women with 5 X chromsomes.
** X chromosomes within a cell, except for the first, are inactivated and segregated as a Barr body within the nucleus. The presence of a Barr body is a common basis for chromosomal tests, used to diagnose sex chromosome aneuploidies (see above).
*** platelets aren't really cells, they're more cell-fragment-buds from megakaryocytes. They still have
strong cell vibes though.