@article {Fr{\"u}hwald501, author = {Michael C Fr{\"u}hwald and M Sue O{\textquoteright}Dorisio and Laura J Rush and Jill L Reiter and Dominic J Smiraglia and Gail Wenger and Joseph F Costello and Peter S White and Ralf Krahe and Garrett M Brodeur and Christoph Plass}, title = {Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon}, volume = {37}, number = {7}, pages = {501--509}, year = {2000}, doi = {10.1136/jmg.37.7.501}, publisher = {BMJ Publishing Group Ltd}, abstract = {OBJECTIVES The pathological entity of primitive neuroectodermal tumour/medulloblastoma (PNET/MB) comprises a very heterogeneous group of neoplasms on a clinical as well as on a molecular level. We evaluated the importance of DNA amplification in medulloblastomas and other primitive neuroectodermal tumours (PNETs) of the CNS. METHOD Restriction landmark genomic scanning (RLGS), a method that allows the detection of low level amplification, was used. RLGS provides direct access to DNA sequences circumventing positional cloning efforts. Furthermore, we analysed several samples by CGH. DESIGN Twenty primary medulloblastomas, five supratentorial PNETs, and five medulloblastoma cell lines were studied. RESULTS Although our analysis confirms that gene amplification is generally a rare event in childhood PNET/MB, we found a total of 17 DNA fragments that were amplified in seven different tumours. Cloning and sequencing of several of these fragments confirmed the previous finding ofMYC amplification in the cell line D341 Med and identified novel DNA sequences amplified in PNET/MB. We describe for the first time amplification of the novel gene,NAG, in a subset of PNET/MB. Despite genomic amplification, NAG was not overexpressed in the tumours studied. We have determined thatNAG maps less than 50 kb 5' ofDDX1 and approximately 400 kb telomeric ofMYCN on chromosome 2p24. CONCLUSION We found a similar but slightly higher frequency of amplification than previously reported. We present several DNA fragments that may belong to the CpG islands of novel genes amplified in a small subset of PNET/MB. As an example we describe for the first time the amplification ofNAG in the MYCNamplicon in PNET/MB.}, issn = {0022-2593}, URL = {https://jmg.bmj.com/content/37/7/501}, eprint = {https://jmg.bmj.com/content/37/7/501.full.pdf}, journal = {Journal of Medical Genetics} }