Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping. Issue 3 (16th June 2022)
- Record Type:
- Journal Article
- Title:
- Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping. Issue 3 (16th June 2022)
- Main Title:
- Detection of cryptic balanced chromosomal rearrangements using high-resolution optical genome mapping
- Authors:
- Zhang, Shuo
Pei, Zhenle
Lei, Caixia
Zhu, Saijuan
Deng, Ke
Zhou, Jing
Yang, Jingmin
Lu, Daru
Sun, Xiaoxi
Xu, Chenming
Xu, Congjian - Abstract:
- Abstract : Background: Chromosomal rearrangements have profound consequences in diverse human genetic diseases. Currently, the detection of balanced chromosomal rearrangements (BCRs) mainly relies on routine cytogenetic G-banded karyotyping. However, cryptic BCRs are hard to detect by karyotyping, and the risk of miscarriage or delivering abnormal offspring with congenital malformations in carrier couples is significantly increased. In the present study, we aimed to investigate the potential of single-molecule optical genome mapping (OGM) in unravelling cryptic chromosomal rearrangements. Methods: Eleven couples with normal karyotypes that had abortions/affected offspring with unbalanced rearrangements were enrolled. Ultra-high-molecular-weight DNA was isolated from peripheral blood cells and processed via OGM. The genome assembly was performed followed by variant calling and annotation. Meanwhile, multiple detection strategies, including FISH, long-range-PCR amplicon-based next-generation sequencing and Sanger sequencing were implemented to confirm the results obtained from OGM. Results: High-resolution OGM successfully detected cryptic reciprocal translocation in all recruited couples, which was consistent with the results of FISH and sequencing. All high-confidence cryptic chromosomal translocations detected by OGM were confirmed by sequencing analysis of rearrangement breakpoints. Moreover, OGM revealed additional complex rearrangement events such as invertedAbstract : Background: Chromosomal rearrangements have profound consequences in diverse human genetic diseases. Currently, the detection of balanced chromosomal rearrangements (BCRs) mainly relies on routine cytogenetic G-banded karyotyping. However, cryptic BCRs are hard to detect by karyotyping, and the risk of miscarriage or delivering abnormal offspring with congenital malformations in carrier couples is significantly increased. In the present study, we aimed to investigate the potential of single-molecule optical genome mapping (OGM) in unravelling cryptic chromosomal rearrangements. Methods: Eleven couples with normal karyotypes that had abortions/affected offspring with unbalanced rearrangements were enrolled. Ultra-high-molecular-weight DNA was isolated from peripheral blood cells and processed via OGM. The genome assembly was performed followed by variant calling and annotation. Meanwhile, multiple detection strategies, including FISH, long-range-PCR amplicon-based next-generation sequencing and Sanger sequencing were implemented to confirm the results obtained from OGM. Results: High-resolution OGM successfully detected cryptic reciprocal translocation in all recruited couples, which was consistent with the results of FISH and sequencing. All high-confidence cryptic chromosomal translocations detected by OGM were confirmed by sequencing analysis of rearrangement breakpoints. Moreover, OGM revealed additional complex rearrangement events such as inverted aberrations, further refining potential genetic interpretation. Conclusion: To the best of our knowledge, this is the first study wherein OGM facilitate the rapid and robust detection of cryptic chromosomal reciprocal translocations in clinical practice. With the excellent performance, our findings suggest that OGM is well qualified as an accurate, comprehensive and first-line method for detecting cryptic BCRs in routine clinical testing. … (more)
- Is Part Of:
- Journal of medical genetics. Volume 60:Issue 3(2023)
- Journal:
- Journal of medical genetics
- Issue:
- Volume 60:Issue 3(2023)
- Issue Display:
- Volume 60, Issue 3 (2023)
- Year:
- 2023
- Volume:
- 60
- Issue:
- 3
- Issue Sort Value:
- 2023-0060-0003-0000
- Page Start:
- 274
- Page End:
- 284
- Publication Date:
- 2022-06-16
- Subjects:
- chromosome aberrations -- reproductive health -- genetic testing -- in situ hybridization, fluorescence -- chromosome banding
Medical genetics -- Periodicals
616.042 - Journal URLs:
- http://jmg.bmjjournals.com/ ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jmedgenet-2022-108553 ↗
- Languages:
- English
- ISSNs:
- 1468-6244
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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