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During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).

During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.

If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).

If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.

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12y ago

During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).

During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.

If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).

If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.

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12y ago

During meiosis I of a primary spermatocyte (an immature sperm cell that hasn't gone through either round of meiosis yet), the homologous chromosomes are supposed to separate, so the XX and YY chromosomes should separate into two different secondary spermatocytes (I wrote XX and YY since there are two sister chromatids for each chromosome). If non-disjunction occurs here, you'd get an one secondary spermatocyte with XXYY and one with no sex chromosomes (so, that's the answer to your question).

During meiosis II, this sister chromatids separate (i.e. XX separates so that one X is given to each cell, and so on with the rest of the chromosomes). In the XXYY spermatocyte, one copy of X and one copy of Y go to each daughter cell as the sister chromatids separate. This results in two XY spermatids and two spermatids with no sex chromosomes being produced (as long as there isn't another non-disjunction). Then they eventually becoming a mature sperm.

If one of those XY sperm ever makes its way to an egg and fertilizes it, you'd get an XXY zygote (which would usually be viable and always male).

If one of the sex-chromosome-less sperm fertilizes an egg, the zygote would be X0 (female), but probably wouldn't be viable and die in utero.

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10y ago

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Q: Which one could produce a sperm with two x chromosomes nondisjunction during meiosis 1 or nondisjunction during meiosis 2?
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Related questions

Nondisjunction occurs when?

homologous chromosomes fail to separate during meiosis


What is it called when chromosomes don't separate correctly during meiosis?

Nondisjunction


What happens during meiosis that ultimately results in a defect characterized by the deletion of chromosomes?

Nondisjunction occurs in too many cells or too few cells causing defects


Failuare of homologous chromosomes to separate properly during meiosis result in gametes with too many or too few chromosomes?

nondisjunction


Occurs during prophase 1 of meiosis?

Mistakes such as nondisjunction can occur during meiosis. This is the result of chromosomes failing to separate equally during either anaphase.


What are nondisjunction genes?

Nondisjunction is the failure of homologous chromosomes or chromatids to segregate during mitosis or meisos with the result that one daughter cell has both of a pair of parental chromosomes or chromatids and the other has none. An example is Trisomy 21, which is also called Down's Syndrome. This person has 3 chromosome #21.Nondisjunction of genes occur during meiosis I when homologous chromosomes fail to separate or during meiosis II when there is unequal distribution of chromosomes. This leads to aneuploidy.


What does klinefelters syndrome come from what type of mutation?

Nondisjunction, or sending both chromosomes to one cell during meiosis.


Is fragile x syndrome a result of nondisjunction during meiosis?

yes . it is . nondisjunction is takes place during meiosis.


If nondisjunction occurs during meiosis?

It is the failure of chromosome pairs to separate properly during cell division.


A human cell may have more or less than 46 chromosomes as a result of nondisjunction a process in what?

chromosomes fail to separate during cell division


What causes disorders sush as klinefelter syndrome and turner syndrome?

non disjunction of sex chromosomes


The faillure of chromosomes to separate during meiosis is called?

Its called disconjunction. Sometimes it is so bad that they have a miscarriage or the following happens:Trisomy (extra chromosomeso have 47 chromosomes instead of 46)Down's syndrome (andextra number 21 chromosome)Klinefelter's syndrome (males with an extra X chromosome...XXY)