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1
Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS.桡侧多指/复拇指与长程顺式调控元件 ZRS 中的新点突变家族中的转录因子结合亲和力改变有关。
Eur J Hum Genet. 2010 Jun;18(6):733-6. doi: 10.1038/ejhg.2009.225. Epub 2010 Jan 13.
2
Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.三个患有三指拇指和轴前多指畸形的家族中,长程SHH增强子出现两个新的点突变。
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3
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A novel mutation in the SHH long-range regulator (ZRS) is associated with preaxial polydactyly, triphalangeal thumb, and severe radial ray deficiency.一个新的 SHH 长距调控区(ZRS)突变与桡侧多指、三叉手和严重的桡侧射线缺如相关。
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Variable expression of subclinical phenotypes instead of reduced penetrance in families with mild triphalangeal thumb phenotypes.家族性轻度三叉手拇指表型中,亚临床表型的可变表达而非外显率降低。
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A novel ZRS mutation leads to preaxial polydactyly type 2 in a heterozygous form and Werner mesomelic syndrome in a homozygous form.一种新的ZRS突变以杂合形式导致2型轴前多指畸形,以纯合形式导致维尔纳中肢发育不全综合征。
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Variable expression of subclinical phenotypes instead of reduced penetrance in families with mild triphalangeal thumb phenotypes.家族性轻度三叉手拇指表型中,亚临床表型的可变表达而非外显率降低。
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A multidisciplinary review of triphalangeal thumb.三指节拇指的多学科综述。
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本文引用的文献

1
HnRNP U mediates the long-range regulation of Shh expression during limb development.HnRNP U在肢体发育过程中介导Shh表达的远程调控。
Hum Mol Genet. 2009 Aug 15;18(16):3090-7. doi: 10.1093/hmg/ddp250. Epub 2009 May 28.
2
A variant in the sonic hedgehog regulatory sequence (ZRS) is associated with triphalangeal thumb and deregulates expression in the developing limb.音猬因子调控序列(ZRS)中的一个变异与三指节拇指相关,并在发育中的肢体中使表达失调。
Hum Mol Genet. 2008 Aug 15;17(16):2417-23. doi: 10.1093/hmg/ddn141. Epub 2008 May 7.
3
Triphalangeal thumb-polysyndactyly syndrome and syndactyly type IV are caused by genomic duplications involving the long range, limb-specific SHH enhancer.三指节拇指-多指并指综合征和IV型并指是由涉及长程、肢体特异性SHH增强子的基因组重复引起的。
J Med Genet. 2008 Sep;45(9):589-95. doi: 10.1136/jmg.2008.057646. Epub 2008 Apr 16.
4
A microduplication of the long range SHH limb regulator (ZRS) is associated with triphalangeal thumb-polysyndactyly syndrome.长程音猬因子肢体调节基因(ZRS)的微重复与三指节拇指-多指畸形综合征相关。
J Med Genet. 2008 Jun;45(6):370-5. doi: 10.1136/jmg.2007.055699. Epub 2008 Jan 4.
5
Point mutations in a distant sonic hedgehog cis-regulator generate a variable regulatory output responsible for preaxial polydactyly.在一个远距离的音猬因子顺式调控元件中的点突变产生了一种可变的调控输出,该输出导致了轴前多指畸形。
Hum Mol Genet. 2008 Apr 1;17(7):978-85. doi: 10.1093/hmg/ddm370. Epub 2007 Dec 21.
6
Two novel point mutations in the long-range SHH enhancer in three families with triphalangeal thumb and preaxial polydactyly.三个患有三指拇指和轴前多指畸形的家族中,长程SHH增强子出现两个新的点突变。
Am J Med Genet A. 2007 Jan 1;143A(1):27-32. doi: 10.1002/ajmg.a.31563.
7
A series of ENU-induced single-base substitutions in a long-range cis-element altering Sonic hedgehog expression in the developing mouse limb bud.一系列ENU诱导的长程顺式元件单碱基替换改变了发育中小鼠肢芽中 Sonic hedgehog 的表达。
Genomics. 2007 Feb;89(2):207-14. doi: 10.1016/j.ygeno.2006.09.005. Epub 2006 Oct 13.
8
Elimination of a long-range cis-regulatory module causes complete loss of limb-specific Shh expression and truncation of the mouse limb.消除一个长程顺式调控模块会导致肢体特异性 Sonic Hedgehog(Shh)表达完全丧失以及小鼠肢体截断。
Development. 2005 Feb;132(4):797-803. doi: 10.1242/dev.01613.
9
Phylogenetic conservation of a limb-specific, cis-acting regulator of Sonic hedgehog ( Shh).音猬因子(Shh)肢体特异性顺式作用调节因子的系统发育保守性
Mamm Genome. 2004 Jan;15(1):23-34. doi: 10.1007/s00335-033-2317-5.
10
A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly.一个远距离的 Sonic Hedgehog(Shh)增强子调控发育中的肢体和鳍中的表达,并与多指(趾)畸形相关。
Hum Mol Genet. 2003 Jul 15;12(14):1725-35. doi: 10.1093/hmg/ddg180.

桡侧多指/复拇指与长程顺式调控元件 ZRS 中的新点突变家族中的转录因子结合亲和力改变有关。

Preaxial polydactyly/triphalangeal thumb is associated with changed transcription factor-binding affinity in a family with a novel point mutation in the long-range cis-regulatory element ZRS.

机构信息

Human Molecular Genetics Laboratory, Health Biotechnology Division, National Institute for Biotechnology & Genetic Engineering (NIBGE), Faisalabad, Pakistan.

出版信息

Eur J Hum Genet. 2010 Jun;18(6):733-6. doi: 10.1038/ejhg.2009.225. Epub 2010 Jan 13.

DOI:10.1038/ejhg.2009.225
PMID:20068592
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2987342/
Abstract

A cis-regulatory sequence also known as zone of polarizing activity (ZPA) regulatory sequence (ZRS) located in intron 5 of LMBR1 is essential for expression of sonic hedgehog (SHH) in the developing posterior limb bud mesenchyme. Even though many point mutations causing preaxial duplication defects have been reported in ZRS, the underlying regulatory mechanism is still unknown. In this study, we analyzed the effect on transcription factor binding of a novel ZRS point mutation (463T>G) in a Pakistani family with preaxial polydactyly and triphalangeal thumb. Electrophoretical mobility shift assay demonstrated a marked difference between wild-type and the mutant probe, which uniquely bound one or several transcription factors extracted from Caco-2 cells. This finding supports a model in which ectopic anterior SHH expression in the developing limb results from abnormal binding of one or more transcription factors to the mutant sequence.

摘要

一个顺式调控序列也被称为极性活动区(ZPA)调控序列(ZRS),位于 LMBR1 内含子 5 中,对于 sonic hedgehog(SHH)在发育中的后肢芽间充质中的表达是必需的。尽管已经报道了许多导致前轴重复缺陷的 ZRS 点突变,但潜在的调控机制仍然未知。在这项研究中,我们分析了一个巴基斯坦多指并三指畸形家族中 ZRS 点突变(463T>G)对转录因子结合的影响。电泳迁移率变动分析显示,野生型和突变探针之间存在显著差异,突变探针仅与从 Caco-2 细胞中提取的一个或多个转录因子结合。这一发现支持了这样一种模型,即发育中的肢体中异常的前 SHH 表达是由于一个或多个转录因子与突变序列的异常结合所致。