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PMID: 12384794 Published · ppublish English Comment Letter

Molecular characterisation of t(17;22)(q11.2;q11.2) is not consistent with NF1 gene duplication.

Human genetics ·Vol. 111 ·No. 4-5 ·2002-10-00 ·页码 465-7; author reply 468-9

Kehrer-Sawatzki H, Assum G, Hameister H

Abstract

A tandem duplication of the NF1 gene in 17q11.2 has recently been detected by high-resolution fluorescence in situ hybridisation (FISH) on stretched chromosomes and DNA fibres. These findings suggest not only that, in the 17q11.2 region, the NF1 gene is surrounded by NF1 low-copy repeats on each side of the gene, but also that the NF1 gene and its directly flanking regions are duplicated structures. However, if the NF1 gene is duplicated at 17q11.2, this should be observed by FISH analysis on metaphase chromosomes of relevant translocation carriers with the probes originally used to identify the duplication, since hybridisation signals of some of the probes would be expected on both derivative chromosomes, the der(17) and the der(22). We have only been able to obtain signals on the one or the other derivative of a female translocation carrier. Therefore, our results do not support the hypothesis of a duplication of the NF1 gene and its immediately flanking regions at 17q11.2 as had been previously postulated. Rather, our findings suggest that there is one NF1 gene in the 17q11.2 region.

MeSH 主题词
Chromosomes, Human, Pair 17 Chromosomes, Human, Pair 22 Gene Duplication Genes, Neurofibromatosis 1 Humans In Situ Hybridization, Fluorescence Molecular Sequence Data Neurofibromatosis 1/genetics Translocation, Genetic
作者与单位
共 3 位作者,点击展开单位 / ORCID
Kehrer-Sawatzki Hildegard
Assum Günter
Hameister Horst
Article Info
Journal
Human genetics
Abbr.
Hum Genet
ISSN
0340-6717
Published
2002-10-00
电子出版
2002-00-24
页码
465-7; author reply 468-9
Language
English
Country/Region
Germany
NLM ID
7613873
数据资源
GENBANK
AC003101
勘误 / 撤稿关联
CommentOn
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