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胚系 PTPN11(HGNC:9644)变异的选择对 Noonan 综合征的高出生率和导致胎儿异常的散发性癌症变异的传播都有重要贡献。

Germline selection of PTPN11 (HGNC:9644) variants make a major contribution to both Noonan syndrome's high birth rate and the transmission of sporadic cancer variants resulting in fetal abnormality.

机构信息

Department of Biological Sciences, Molecular and Computational Biology Program, University of Southern California, Los Angeles, California, USA.

Department of Chemistry, Bridge Institute, University of Southern California, Los Angeles, California, USA.

出版信息

Hum Mutat. 2022 Dec;43(12):2205-2221. doi: 10.1002/humu.24493. Epub 2022 Nov 24.

DOI:10.1002/humu.24493
PMID:36349709
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10099774/
Abstract

Some spontaneous germline gain-of-function mutations promote spermatogonial stem cell clonal expansion and disproportionate variant sperm production leading to unexpectedly high transmission rates for some human genetic conditions. To measure the frequency and spatial distribution of de novo mutations we divided three testes into 192 pieces each and used error-corrected deep-sequencing on each piece. We focused on PTPN11 (HGNC:9644) Exon 3 that contains 30 different PTPN11 Noonan syndrome (NS) mutation sites. We found 14 of these variants formed clusters among the testes; one testis had 11 different variant clusters. The mutation frequencies of these different clusters were not correlated with their case-recurrence rates nor were case recurrence rates of PTPN11 variants correlated with their tyrosine phosphatase levels thereby confusing PTPN11's role in germline clonal expansion. Six of the PTPN11 exon 3 de novo variants associated with somatic mutation-induced sporadic cancers (but not NS) also formed testis clusters. Further, three of these six variants were observed among fetuses that underwent prenatal ultrasound screening for NS-like features. Mathematical modeling showed that germline selection can explain both the mutation clusters and the high incidence of NS (1/1000-1/2500).

摘要

一些自发的种系获得性功能突变促进精原干细胞克隆扩增和不成比例的变异精子产生,导致一些人类遗传疾病的意外高传播率。为了测量新生突变的频率和空间分布,我们将三个睾丸分为 192 块,对每一块进行纠错深度测序。我们集中研究含有 30 个不同 Noonan 综合征(NS)突变位点的 PTPN11(HGNC:9644)外显子 3。我们发现这些变体中有 14 个在睾丸中形成簇;一个睾丸有 11 个不同的变体簇。这些不同簇的突变频率与其病例复发率无关,PTPN11 变体的病例复发率也与其酪氨酸磷酸酶水平无关,从而混淆了 PTPN11 在种系克隆扩增中的作用。与体细胞突变诱导的散发性癌症(而非 NS)相关的 PTPN11 外显子 3 的 6 个新生变体也形成了睾丸簇。此外,在接受 NS 样特征产前超声筛查的胎儿中观察到这 6 个变体中的 3 个。数学模型表明,种系选择可以解释突变簇和 NS 的高发生率(1/1000-1/2500)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/8826dfc75f40/HUMU-43-2205-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/69ed3d2f7459/HUMU-43-2205-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/73ecc7fd706f/HUMU-43-2205-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/a346161861fe/HUMU-43-2205-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/5fb7d41fd10f/HUMU-43-2205-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/ce37c4fc6038/HUMU-43-2205-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/8826dfc75f40/HUMU-43-2205-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/69ed3d2f7459/HUMU-43-2205-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/73ecc7fd706f/HUMU-43-2205-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/a346161861fe/HUMU-43-2205-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/5fb7d41fd10f/HUMU-43-2205-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/ce37c4fc6038/HUMU-43-2205-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5124/10099774/8826dfc75f40/HUMU-43-2205-g002.jpg

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