Human Genetics

, Volume 137, Issue 6–7, pp 511–520 | Cite as

Extreme clustering of type-1 NF1 deletion breakpoints co-locating with G-quadruplex forming sequences

  • Anna Summerer
  • Victor-Felix Mautner
  • Meena Upadhyaya
  • Kathleen B. M. Claes
  • Josef Högel
  • David N. Cooper
  • Ludwine Messiaen
  • Hildegard Kehrer-Sawatzki
Original Investigation


The breakpoints of type-1 NF1 deletions encompassing 1.4-Mb are located within NF1-REPa and NF1-REPc, which exhibit a complex structure comprising different segmental duplications in direct and inverted orientation. Here, we systematically assessed the proportion of type-1 NF1 deletions caused by nonallelic homologous recombination (NAHR) and those mediated by other mutational mechanisms. To this end, we analyzed 236 unselected type-1 deletions and observed that 179 of them (75.8%) had breakpoints located within the NAHR hotspot PRS2, whereas 39 deletions (16.5%) had breakpoints located within PRS1. Sixteen deletions exhibited breakpoints located outside of these NAHR hotspots but were also mediated by NAHR. Taken together, the breakpoints of 234 (99.2%) of the 236 type-1 NF1 deletions were mediated by NAHR. Thus, NF1-REPa and NF1-REPc are strongly predisposed to recurrent NAHR, the main mechanism underlying type-1 NF1 deletions. We also observed a non-random overlap between type-1 NF1-deletion breakpoints and G-quadruplex forming sequences (GQs) as well as regions flanking PRDM9A binding-sites. These findings imply that GQs and PRDM9A binding-sites contribute to the clustering of type-1 deletion breakpoints. The co-location of both types of sequence was at its highest within PRS2, indicative of their synergistic contribution to the greatly increased NAHR activity within this hotspot.



This work has been funded by the Deutsche Forschungsgemeinschaft (DFG) Grant KE 724/12-2.

Compliance with ethical standards

Conflict of interest

On behalf of all authors, the corresponding author states that there is no conflict of interest.

Supplementary material

439_2018_1904_MOESM1_ESM.pdf (3.4 mb)
Supplementary material 1 (PDF 3502 KB)


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Copyright information

© Springer-Verlag GmbH Germany, part of Springer Nature 2018

Authors and Affiliations

  1. 1.Institute of Human GeneticsUniversity of UlmUlmGermany
  2. 2.Department of NeurologyUniversity Hospital Hamburg EppendorfHamburgGermany
  3. 3.Institute of Medical Genetics, School of MedicineCardiff UniversityCardiffUK
  4. 4.Center for Medical Genetics GhentGhent University HospitalGhentBelgium
  5. 5.Department of GeneticsUniversity of Alabama at BirminghamBirminghamUSA

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