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近端15q的遗传性间质重复:基因型与表型的相关性

Inherited interstitial duplications of proximal 15q: genotype-phenotype correlations.

作者信息

Browne C E, Dennis N R, Maher E, Long F L, Nicholson J C, Sillibourne J, Barber J C

机构信息

Wessex Regional Genetics Laboratory, Salisbury District Hospital, United Kingdom.

出版信息

Am J Hum Genet. 1997 Dec;61(6):1342-52. doi: 10.1086/301624.

DOI:10.1086/301624
PMID:9399882
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1716086/
Abstract

We present the cytogenetic, molecular cytogenetic, and molecular genetic results on 20 unrelated patients with an interstitial duplication of the proximal long arm of chromosome 15. Multiple probes showed that the Prader-Willi/Angelman critical region (PWACR) was included in the duplication in 4/20 patients, each ascertained with developmental delay. The duplication was also found in two affected but not in three unaffected sibs of one of these patients. All four probands had inherited their duplication from their mothers, three of whom were also affected. Two of the affected mothers also carried a maternally inherited duplication, whereas the duplication in the unaffected mother and in an unaffected grandmother was paternal in origin, raising the possibility of a parental-origin effect. The PWACR was not duplicated in the remaining 16 patients, of whom 4 were referred with developmental delay. In the 14 families for which parental samples were available, the duplication was inherited with equal frequency from a phenotypically normal parent, mother or father. Comparative genomic hybridization undertaken on two patients suggested that proximal 15q outside the PWACR was the origin of the duplicated material. The use of PWACR probes discriminates between a large group of duplications of no apparent clinical significance and a smaller group, in which a maternally derived PWACR duplication is consistently associated with developmental delay and speech difficulties but not with overt features of either Prader-Willi syndrome or Angelman syndrome.

摘要

我们展示了20例非亲缘关系的15号染色体长臂近端间质性重复患者的细胞遗传学、分子细胞遗传学和分子遗传学结果。多个探针显示,在20例患者中有4例的重复区域包含普拉德-威利/安吉尔曼临界区域(PWACR),这4例均因发育迟缓确诊。在其中1例患者的2名患病同胞中也发现了该重复,但在3名未患病同胞中未发现。所有4例先证者的重复均遗传自其母亲,其中3名母亲也患病。2名患病母亲也携带母系遗传的重复,而未患病母亲和1名未患病祖母的重复来源于父系,这增加了亲本来源效应的可能性。其余16例患者的PWACR未发生重复,其中4例因发育迟缓前来就诊。在可获取亲本样本的14个家庭中,该重复从表型正常的亲本(母亲或父亲)遗传而来的频率相同。对2例患者进行的比较基因组杂交表明,PWACR以外的15q近端是重复片段的来源。使用PWACR探针可区分一大组无明显临床意义的重复和一小组重复,其中母系来源的PWACR重复始终与发育迟缓和言语困难相关,但与普拉德-威利综合征或安吉尔曼综合征的明显特征无关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/1c2a27738bb5/ajhg00012-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/cb9cf3482e48/ajhg00012-0139-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/84a9d271dfe7/ajhg00012-0141-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/067da5052ffa/ajhg00012-0143-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/31f04543e760/ajhg00012-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/1c2a27738bb5/ajhg00012-0146-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/cb9cf3482e48/ajhg00012-0139-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/84a9d271dfe7/ajhg00012-0141-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/067da5052ffa/ajhg00012-0143-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/31f04543e760/ajhg00012-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8b23/1716086/1c2a27738bb5/ajhg00012-0146-a.jpg

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2
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Eur J Hum Genet. 1996;4(2):88-100. doi: 10.1159/000472176.
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Good genes in bad neighbourhoods.身处不良环境中的优良基因。
J Appl Genet. 2023 May;64(2):303-317. doi: 10.1007/s13353-022-00742-8. Epub 2023 Jan 30.
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Genetic dissection identifies Necdin as a driver gene in a mouse model of paternal 15q duplications.遗传剖析确定 Necdin 为父源 15q 重复小鼠模型中的驱动基因。
Nat Commun. 2021 Jul 1;12(1):4056. doi: 10.1038/s41467-021-24359-3.
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Rare partial octosomy and hexasomy of 15q11-q13 associated with intellectual impairment and development delay: report of two cases and review of literature.与智力障碍和发育迟缓相关的罕见的15q11 - q13部分八体性和六体性:两例报告及文献复习
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