Bijlsma E K, Merel P, Bosch D A, Westerveld A, Delattre O, Thomas G, Hulsebos T J
Institute of Human Genetics, Academic Medical Centre, University of Amsterdam, The Netherlands.
Genes Chromosomes Cancer. 1994 Sep;11(1):7-14. doi: 10.1002/gcc.2870110103.
Schwannomas are benign tumors of cranial, spinal, and other nerve sheaths that develop sporadically or are inherited as part of neurofibromatosis type 2 (NF2). The NF2 gene (SCH) on chromosome 22 has recently been identified and shown to be inactivated by mutation and allele loss in some schwannomas. However, only limited regions in the SCH coding region were examined for mutations. We have extended these studies by screening virtually all coding sequences of the SCH gene (95% coverage) and adjacent splice site sequences for the presence of mutations in 48 schwannomas. All tumors (34 vestibular schwannomas and 14 schwannomas of other locations) were additionally characterized for allele loss on chromosome 22. By PCR-DGGE screening of the 16 known exons of the SCH gene, 22 mutations were found. Most of these give rise to a premature stop codon and are expected to result in the synthesis of a truncated gene product (schwannomin). Although there was no apparent hotspot for mutations, 16 of the 22 mutations occurred in the first eight exons or adjacent splice site sequences of the SCH gene. In several vestibular as well as other schwannomas loss of one SCH allele and mutational inactivation of the second allele were identified in the same tumor. Our data indicate that the SCH gene is implicated in the development of schwannomas of all locations in the nervous system.
施万细胞瘤是颅神经、脊神经及其他神经鞘的良性肿瘤,可散发发生,或作为2型神经纤维瘤病(NF2)的一部分而遗传。22号染色体上的NF2基因(SCH)最近已被鉴定出来,并且在一些施万细胞瘤中显示因突变和等位基因缺失而失活。然而,仅对SCH编码区的有限区域进行了突变检测。我们通过筛查48例施万细胞瘤中SCH基因的几乎所有编码序列(95%覆盖率)及相邻剪接位点序列中的突变,扩展了这些研究。所有肿瘤(34例前庭神经鞘瘤和14例其他部位的神经鞘瘤)还进行了22号染色体等位基因缺失的特征分析。通过PCR-DGGE筛查SCH基因的16个已知外显子,发现了22个突变。其中大多数会产生提前终止密码子,预计会导致截短的基因产物(施万蛋白)的合成。虽然没有明显的突变热点,但22个突变中有16个发生在SCH基因的前8个外显子或相邻剪接位点序列中。在一些前庭神经鞘瘤以及其他神经鞘瘤中,在同一肿瘤中鉴定出一个SCH等位基因缺失,另一个等位基因发生突变失活。我们的数据表明,SCH基因与神经系统所有部位的神经鞘瘤的发生有关。