• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

POU1F1 内含子变异与犬垂体性侏儒症相关。

Intronic variant in POU1F1 associated with canine pituitary dwarfism.

机构信息

Department of Medical and Clinical Genetics, University of Helsinki, Helsinki, Finland.

Department of Veterinary Biosciences, University of Helsinki, Helsinki, Finland.

出版信息

Hum Genet. 2021 Nov;140(11):1553-1562. doi: 10.1007/s00439-021-02259-2. Epub 2021 Feb 6.

DOI:10.1007/s00439-021-02259-2
PMID:33550451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8519942/
Abstract

The anterior pituitary gland secretes several endocrine hormones, essential for growth, reproduction and other basic physiological functions. Abnormal development or function of the pituitary gland leads to isolated or combined pituitary hormone deficiency (CPHD). At least 30 genes have been associated with human CPHD, including many transcription factors, such as POU1F1. CPHD occurs spontaneously also in mice and dogs. Two affected breeds have been reported in dogs: German Shepherds with a splice defect in the LHX3 gene and Karelian Bear Dogs (KBD) with an unknown genetic cause. We obtained samples from five KBDs presenting dwarfism and abnormal coats. A combined analysis of genome-wide association and next-generation sequencing mapped the disease to a region in chromosome 31 and identified a homozygous intronic variant in the fourth exon of the POU1F1 gene in the affected dogs. The identified variant, c.605-3C>A, resided in the splice region and was predicted to affect splicing. The variant's screening in three new prospective cases, related breeds, and ~ 8000 dogs from 207 breeds indicated complete segregation in KBDs with a carrier frequency of 8%, and high breed-specificity as carriers were found at a low frequency only in Lapponian Herders, a related breed. Our study establishes a novel canine model for CPHD with a candidate POU1F1 defect.

摘要

垂体前叶分泌多种内分泌激素,对生长、繁殖和其他基本生理功能至关重要。垂体发育或功能异常可导致孤立性或联合性垂体激素缺乏症(CPHD)。至少有 30 个基因与人类 CPHD 有关,包括许多转录因子,如 POU1F1。CPHD 在小鼠和犬中也自发发生。在犬中已经报道了两种受影响的品种:LHX3 基因剪接缺陷的德国牧羊犬和原因不明的遗传的 Karelian 熊犬(KBD)。我们从 5 只表现为矮小症和异常被毛的 KBD 中获得了样本。全基因组关联分析和下一代测序的联合分析将该疾病定位到染色体 31 上的一个区域,并在受影响的犬中鉴定出 POU1F1 基因第四外显子中的纯合内含子变异。鉴定出的变异,c.605-3C>A,位于剪接区,预计会影响剪接。该变异在三个新的前瞻性病例、相关品种和 207 个品种的~8000 只犬中的筛查表明,KBD 中存在完全分离,携带频率为 8%,并且仅在相关品种拉普兰牧羊犬中以低频率发现高品种特异性携带。我们的研究建立了一种新的 CPHD 犬模型,候选 POU1F1 缺陷。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/ee659bb0b49c/439_2021_2259_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/8fd271ed68d4/439_2021_2259_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/f1ef4c1d3396/439_2021_2259_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/ee659bb0b49c/439_2021_2259_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/8fd271ed68d4/439_2021_2259_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/f1ef4c1d3396/439_2021_2259_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fce9/8519942/ee659bb0b49c/439_2021_2259_Fig3_HTML.jpg

相似文献

1
Intronic variant in POU1F1 associated with canine pituitary dwarfism.POU1F1 内含子变异与犬垂体性侏儒症相关。
Hum Genet. 2021 Nov;140(11):1553-1562. doi: 10.1007/s00439-021-02259-2. Epub 2021 Feb 6.
2
Cloning of the canine gene encoding transcription factor Pit-1 and its exclusion as candidate gene in a canine model of pituitary dwarfism.犬类编码转录因子Pit-1基因的克隆及其在垂体性侏儒症犬模型中作为候选基因的排除。
Mamm Genome. 2000 Jan;11(1):31-6. doi: 10.1007/s003350010006.
3
A novel heterozygous intronic mutation in POU1F1 is associated with combined pituitary hormone deficiency.POU1F1基因中的一种新型杂合内含子突变与垂体激素联合缺乏症相关。
Endocr J. 2017 Feb 27;64(2):229-234. doi: 10.1507/endocrj.EJ16-0361. Epub 2016 Nov 22.
4
A contracted DNA repeat in LHX3 intron 5 is associated with aberrant splicing and pituitary dwarfism in German shepherd dogs.LHX3 内含子 5 中的一个 DNA 重复序列与德国牧羊犬的异常剪接和垂体性矮小相关。
PLoS One. 2011;6(11):e27940. doi: 10.1371/journal.pone.0027940. Epub 2011 Nov 23.
5
Pituitary dwarfism in Saarloos and Czechoslovakian wolfdogs is associated with a mutation in LHX3.萨阿路斯狼犬和捷克斯洛伐克狼犬的垂体性侏儒症与LHX3基因的突变有关。
J Vet Intern Med. 2014 Nov-Dec;28(6):1770-4. doi: 10.1111/jvim.12448. Epub 2014 Oct 1.
6
A mutation of the β-domain in POU1F1 causes pituitary deficiency due to dominant PIT-1β expression.POU1F1 的β-结构域突变导致由于显性 PIT-1β 表达引起的垂体功能减退。
Eur J Endocrinol. 2021 May 21;185(1):1-12. doi: 10.1530/EJE-20-1313.
7
Atlanto-axial malformation and instability in dogs with pituitary dwarfism due to an LHX3 mutation.因LHX3突变导致垂体性侏儒症的犬类寰枢椎畸形与不稳定
J Vet Intern Med. 2015 Jan;29(1):207-13. doi: 10.1111/jvim.12523. Epub 2015 Jan 14.
8
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study.土耳其联合垂体激素缺乏症患者中PROP1、POU1F1、LHX3和HESX1的分子分析:一项多中心研究
Endocrine. 2015 Jun;49(2):479-91. doi: 10.1007/s12020-014-0498-1. Epub 2014 Dec 11.
9
A Novel Splice-Site Deletion in the Gene Causes Combined Pituitary Hormone Deficiency in Multiple Sudanese Pedigrees.一个新的剪接位点缺失导致多个苏丹家系的联合垂体激素缺乏症。
Genes (Basel). 2022 Apr 8;13(4):657. doi: 10.3390/genes13040657.
10
A novel germline mutation, IVS4+1G>A, of the POU1F1 gene underlying combined pituitary hormone deficiency.一种导致联合垂体激素缺乏的POU1F1基因的新型种系突变,IVS4+1G>A。
Horm Res. 2008;69(1):60-4. doi: 10.1159/000111797. Epub 2007 Dec 4.

引用本文的文献

1
A Nonsynonymous Substitution of Leads to Changes in Body Size in Dogs and Mice.一个非同义替换导致狗和老鼠的体型变化。
Genes (Basel). 2024 Jun 4;15(6):739. doi: 10.3390/genes15060739.
2
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human.鉴定扩张型心肌病的新型遗传风险因素:从犬到人类。
Genome Med. 2023 Sep 18;15(1):73. doi: 10.1186/s13073-023-01221-3.
3
Missense Variant in Vizslas with Disproportionate Dwarfism.具有不成比例矮小症的维兹拉犬中的错义变异。

本文引用的文献

1
Clinical lessons learned in constitutional hypopituitarism from two decades of experience in a large international cohort.从一个大型国际队列二十年的经验中汲取的体质性垂体功能减退症的临床教训。
Clin Endocrinol (Oxf). 2021 Feb;94(2):277-289. doi: 10.1111/cen.14355. Epub 2020 Dec 21.
2
webGQT: A Shiny Server for Genotype Query Tools for Model-Based Variant Filtering.网络基因查询工具(webGQT):用于基于模型的变异过滤的基因型查询工具的闪亮服务器。
Front Genet. 2020 Mar 3;11:152. doi: 10.3389/fgene.2020.00152. eCollection 2020.
3
A comprehensive biomedical variant catalogue based on whole genome sequences of 582 dogs and eight wolves.
Genes (Basel). 2022 Dec 13;13(12):2354. doi: 10.3390/genes13122354.
基于 582 只狗和 8 只狼的全基因组序列构建的综合生物医学变异目录。
Anim Genet. 2019 Dec;50(6):695-704. doi: 10.1111/age.12834. Epub 2019 Sep 5.
4
A homozygous missense variant in the alkaline phosphatase gene ALPL is associated with a severe form of canine hypophosphatasia.
Sci Rep. 2019 Jan 30;9(1):973. doi: 10.1038/s41598-018-37801-2.
5
The Mobile Element Locator Tool (MELT): population-scale mobile element discovery and biology.移动元件定位工具(MELT):大规模移动元件发现与生物学。
Genome Res. 2017 Nov;27(11):1916-1929. doi: 10.1101/gr.218032.116. Epub 2017 Aug 30.
6
Genetics of Combined Pituitary Hormone Deficiency: Roadmap into the Genome Era.联合垂体激素缺乏症的遗传学:迈向基因组时代的路线图
Endocr Rev. 2016 Dec;37(6):636-675. doi: 10.1210/er.2016-1101. Epub 2016 Nov 9.
7
Molecular Characterization of Three Canine Models of Human Rare Bone Diseases: Caffey, van den Ende-Gupta, and Raine Syndromes.三种人类罕见骨病犬类模型的分子特征:卡菲病、范登恩德-古普塔综合征和雷恩综合征
PLoS Genet. 2016 May 17;12(5):e1006037. doi: 10.1371/journal.pgen.1006037. eCollection 2016 May.
8
MECHANISMS IN ENDOCRINOLOGY: An update in the genetic aetiologies of combined pituitary hormone deficiency.内分泌学机制:垂体激素联合缺乏症遗传病因学的最新进展
Eur J Endocrinol. 2016 Jun;174(6):R239-47. doi: 10.1530/EJE-15-1095. Epub 2016 Jan 5.
9
Functional characterization of a human POU1F1 mutation associated with isolated growth hormone deficiency: a novel etiology for IGHD.与孤立性生长激素缺乏症相关的人类POU1F1突变的功能特征:一种导致孤立性生长激素缺乏症的新病因。
Hum Mol Genet. 2016 Feb 1;25(3):472-83. doi: 10.1093/hmg/ddv486. Epub 2015 Nov 26.
10
Efficient genotype compression and analysis of large genetic-variation data sets.大型基因变异数据集的高效基因型压缩与分析
Nat Methods. 2016 Jan;13(1):63-5. doi: 10.1038/nmeth.3654. Epub 2015 Nov 9.