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Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors

Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors
Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors
Human trisomy is attributable to many different mechanisms and the relative importance of each mechanism is highly chromosome specific. The association between altered recombination and maternal non-disjunction is well documented: reductions in recombination have been reported for maternal meiosis I (MI) errors involving chromosomes 15, 16, 18 and 21 and increased recombination has been reported for meiosis II (MII) errors involving chromosome 21. We therefore investigated maternal X chromosome non-disjunction, to determine whether the effects of recombination are unique to the X chromosome or similar to any of the autosomes thus far studied. We genotyped 45 47,XXX females and 95 47,XXY males of maternal origin. Our results demonstrate that 49% arose during MI, 29% during MII and 16% were postzygotic events; a further 7% were meiotic but could not be assigned as either MI or MII because of recombination at the centromere. Among the MI cases, a majority (56%) had no detectable transitions and so absent recombination is an important factor for X chromosome non-disjunction. However, similar to trisomy 15 and unlike trisomy 21, we observed a significant increase in the mean maternal age of transitional MI errors compared with nullitransitional cases. In our studies of MII errors, recombination appeared normal and there was no obvious effect of maternal age, distinguishing our results from MII non-disjunction of chromosomes 18 or 21. Thus, surprisingly, the risk factors associated with both MI and MII non-disjunction appear to be different for virtually every chromosome that has been adequately studied.
243-250
Thomas, N. Simon
1a601957-288d-4f12-a9f7-4f4279b7f9b3
Ennis, Sarah
7b57f188-9d91-4beb-b217-09856146f1e9
Sharp, Andrew J.
4f814cb9-0069-4850-ad81-5ad57435f414
Durkie, Miranda
7caca497-e12f-4f13-99e0-f40e767f0163
Hassold, Terry J.
93117e5b-0687-4fd2-9816-97c2972824a0
Collins, Andrew R.
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Jacobs, Patricia A.
d87ec15b-13c3-4868-96f1-b4b99030fa5b
Thomas, N. Simon
1a601957-288d-4f12-a9f7-4f4279b7f9b3
Ennis, Sarah
7b57f188-9d91-4beb-b217-09856146f1e9
Sharp, Andrew J.
4f814cb9-0069-4850-ad81-5ad57435f414
Durkie, Miranda
7caca497-e12f-4f13-99e0-f40e767f0163
Hassold, Terry J.
93117e5b-0687-4fd2-9816-97c2972824a0
Collins, Andrew R.
7daa83eb-0b21-43b2-af1a-e38fb36e2a64
Jacobs, Patricia A.
d87ec15b-13c3-4868-96f1-b4b99030fa5b

Thomas, N. Simon, Ennis, Sarah, Sharp, Andrew J., Durkie, Miranda, Hassold, Terry J., Collins, Andrew R. and Jacobs, Patricia A. (2001) Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factors. Human Molecular Genetics, 10 (3), 243-250. (doi:10.1093/hmg/10.3.243).

Record type: Article

Abstract

Human trisomy is attributable to many different mechanisms and the relative importance of each mechanism is highly chromosome specific. The association between altered recombination and maternal non-disjunction is well documented: reductions in recombination have been reported for maternal meiosis I (MI) errors involving chromosomes 15, 16, 18 and 21 and increased recombination has been reported for meiosis II (MII) errors involving chromosome 21. We therefore investigated maternal X chromosome non-disjunction, to determine whether the effects of recombination are unique to the X chromosome or similar to any of the autosomes thus far studied. We genotyped 45 47,XXX females and 95 47,XXY males of maternal origin. Our results demonstrate that 49% arose during MI, 29% during MII and 16% were postzygotic events; a further 7% were meiotic but could not be assigned as either MI or MII because of recombination at the centromere. Among the MI cases, a majority (56%) had no detectable transitions and so absent recombination is an important factor for X chromosome non-disjunction. However, similar to trisomy 15 and unlike trisomy 21, we observed a significant increase in the mean maternal age of transitional MI errors compared with nullitransitional cases. In our studies of MII errors, recombination appeared normal and there was no obvious effect of maternal age, distinguishing our results from MII non-disjunction of chromosomes 18 or 21. Thus, surprisingly, the risk factors associated with both MI and MII non-disjunction appear to be different for virtually every chromosome that has been adequately studied.

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Published date: 1 February 2001

Identifiers

Local EPrints ID: 24983
URI: http://eprints.soton.ac.uk/id/eprint/24983
PURE UUID: 4fa62670-595c-44a7-9334-8f274e695297
ORCID for Sarah Ennis: ORCID iD orcid.org/0000-0003-2648-0869
ORCID for Andrew R. Collins: ORCID iD orcid.org/0000-0001-7108-0771

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Date deposited: 04 Apr 2006
Last modified: 16 Mar 2024 03:07

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Contributors

Author: N. Simon Thomas
Author: Sarah Ennis ORCID iD
Author: Andrew J. Sharp
Author: Miranda Durkie
Author: Terry J. Hassold
Author: Patricia A. Jacobs

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