Do Humans Have 23 or 46 Chromosomes?

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Discussion Overview

The discussion revolves around the number of chromosomes in humans, specifically addressing the confusion between the concepts of chromosome pairs and individual chromosomes. Participants explore the implications of genetic terminology and the processes involved in cell division, particularly meiosis, as well as the pairing and recombination of sex chromosomes.

Discussion Character

  • Exploratory
  • Technical explanation
  • Conceptual clarification
  • Debate/contested

Main Points Raised

  • Some participants assert that humans have 46 chromosomes, consisting of 22 pairs of autosomal chromosomes and one pair of sex chromosomes (XX or XY).
  • There is confusion regarding whether the term "twenty-three chromosomes" refers to chromosome types or pairs, with some participants suggesting that this could lead to misunderstanding the total count.
  • One participant questions the interpretation of a passage about chromosome division and recombination, seeking clarification on whether the original orientation of chromosomes is lost during this process.
  • Another participant explains that recombination occurs between homologous chromosomes, but the orientation remains unchanged, and the combination of genes is altered.
  • Concerns are raised about the frequency of recombination between X and Y chromosomes, with some participants expressing skepticism about its occurrence.
  • One participant provides a visual example to illustrate how genes can be exchanged during recombination while maintaining the overall number of genes.

Areas of Agreement / Disagreement

Participants generally agree that humans have 46 chromosomes, but there is disagreement and confusion regarding the terminology and processes involved in chromosome pairing and recombination, particularly concerning the X and Y chromosomes.

Contextual Notes

Participants express uncertainty about the definitions and implications of chromosome counts, as well as the specifics of genetic recombination, particularly between sex chromosomes. The discussion highlights the complexity of genetic concepts and the potential for misinterpretation of scientific literature.

Jeebus
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I'm reading a book about genetics, but I'm really confused about chromosomes. It's mainly vocabulary trouble. It is my understanding that the human genome has twenty-three pairs of chromosomes. I commonly hear people say that humans have twenty-three chromosomes, does that mean chromosome types? Because if there are twenty-three pairs, then that would make forty-six, right? The book I'm reading is called The language of Genes by Steve Jones. Here is the particular passage that's messing with me:

"Every cell contains two copies of each of the chromosomes. The number is halved during a special kind of cell division in the testis or ovary. During the process, the chromosomes lie together in their pairs and exchange parts of their structure. Sperm or egg cells hence contain combinations of chromosomal material which differ from those in the cells of the parents who produced them."

Now, when I first started reading this, I initially thought that when it said "every cell contains two copies," it was referring to chromosome pairs (two chromosomes of the same type; one from mom, one from dad). Then it says it halves, so we're left with twenty-three independent chromosomes. Then it says that the chromosomes lie together in their pairs, so then I went back and re-evaluated what it meant when it said "two copies," since based on my initial understanding, after it split in half, there would be no more pairs. So, now, my understanding is that there are forty-six chromosome pairs (which divide into the twenty-three chromosome pairs in the process from the quote). Which would now bring the count of individual chromosomes up to ninety-two.

If I'm wrong (which I'm sure I am), please correct me. According to this picture (http://www.ncrtec.org/tl/camp/gene/male.gif), there are at least forty-six chromosomes (two times twenty-three). I'm totally confused by an apparent lack of clarity in what I'm reading (not clarifying whether it's about pairs of chromosomes or individual chromosomes, I'm just confused here).

http://biology.udayton.edu/MED/SCI230/LECTHELP-2/1DNA-intro.htm - This is another source I was using to clear my confusion. This site further reinforces my idea that there are forty-six.

Can someone straighten me out here?
 
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Hi Jeebus, this topic belongs in Biology, but anyway:

A normal human cell contains 46 chromosomes. There are 22 autosomal chromosomes (which are identical in males and females) and they are numbered 1-22.

Everyone has two autosomal chromosomes of each type. One is passed down from the mother and the other is passed down from the father of the child.

Besides the two copies of autosomal chromosomes (total 44) everyone is supposed to have two sex chromosomes. Females have XX and males have XY. Thus giving you a total of 46 chromosomes.


There are diseases known where people have an abnormal number of chromosomes. Trisomy 21 (three copies of chr. 21) leads to the Down syndrome. Or, XXY leads to Klinefelter syndrome (poor secondary sexual development).
 
Originally posted by Monique
..Everyone has two autosomal chromosomes of each type. One is passed down from the mother and the other is passed down from the father of the child.

Besides the two copies of autosomal chromosomes (total 44) everyone is supposed to have two sex chromosomes. Females have XX and males have XY. Thus giving you a total of 46 chromosomes.

All right. For some reason, I was reading that passage a weird way and I think I get it now. Is the passage saying that as the chromosome pairs are divided, the two chromosomes exchange certain genes back and forth and whatnot right before the division, so the original orientation is lost? Are the X and Y chromosomes actually paired up? If so, why are certain traits always with the X and are never exchanged during this process with the Y? If not, do they just randomly join one of the gametes?
 
Originally posted by Jeebus
Is the passage saying that as the chromosome pairs are divided, the two chromosomes exchange certain genes back and forth and whatnot right before the division, so the original orientation is lost?

The only thing wrong is the orientation lost. The orientation is not changed but the combination of genes on a given chromosome after the exchange (called recombination) is different.

Originally posted by Jeebus
Are the X and Y chromosomes actually paired up? If so, why are certain traits always with the X and are never exchanged during this process with the Y? If not, do they just randomly join one of the gametes?

Yes X and Y more or less paired up and recombination occurs for regions that are share by Y and X. Y is smaller than X and share some homology with X. Some traits are only with X because it is missing from Y and there no recombination in this case. The split up of the chromosome is more or less random. Half will get X and the other will get Y but it is not predetermined which harlf get what.
 
Lets say you have two identical chromosomes which line up:
Code:
AAAAAAAAAAAAAAAAAAAAA
      X   X
BBBBBBBBBBBBBBBBBBBBB
The two X's mark the place of recombination, the result is:

Code:
AAAAAAABBBAAAAAAAAAAA

BBBBBBBAAABBBBBBBBBBB
So in this example 3 genes were exchanged, but the number of genes and the identity of the genes is still the same. The only thing different is the origin of the genes (mixure of paternal/maternal genes).

Ian, I am very surprised that you say that recombinations occur between X and Y. How sure are you of that?
 
Originally posted by Monique
Ian, I am very surprised that you say that recombinations occur between X and Y. How sure are you of that?

It does occur but at very low frequency and sometimes it can lead to problem. X and Y recombination is not a usual event.

http://www.pubmedcentral.nih.gov/articlerender.fcgi?rendertype=abstract&artid=42981
 

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