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本文引用的文献

1
cis-regulatory mutations are a genetic cause of human limb malformations.顺式调控基因突变是人类肢体畸形的一种遗传病因。
Dev Dyn. 2011 May;240(5):920-30. doi: 10.1002/dvdy.22535. Epub 2011 Jan 11.
2
The chicken polydactyly (Po) locus causes allelic imbalance and ectopic expression of Shh during limb development.鸡多指(Po)基因座在肢体发育过程中导致等位基因失衡和 Shh 的异位表达。
Dev Dyn. 2011 May;240(5):1163-72. doi: 10.1002/dvdy.22623. Epub 2011 Apr 4.
3
Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactyly.鉴定出与家族性桡侧多指畸形相关的 Shh 长距调控因子中的两个新突变。
Clin Genet. 2011 Apr;79(4):371-7. doi: 10.1111/j.1399-0004.2010.01465.x.
4
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.
5
Homozygous feature of isolated triphalangeal thumb-preaxial polydactyly linked to 7q36: no phenotypic difference between homozygotes and heterozygotes.与7q36相关的孤立性三指节拇指-轴前多指畸形的纯合特征:纯合子与杂合子之间无表型差异。
Clin Genet. 2009 Jul;76(1):85-90. doi: 10.1111/j.1399-0004.2009.01192.x. Epub 2009 Jun 9.
6
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.
7
UniPROBE: an online database of protein binding microarray data on protein-DNA interactions.UniPROBE:一个关于蛋白质与DNA相互作用的蛋白质结合微阵列数据在线数据库。
Nucleic Acids Res. 2009 Jan;37(Database issue):D77-82. doi: 10.1093/nar/gkn660. Epub 2008 Oct 8.
8
Canine polydactyl mutations with heterogeneous origin in the conserved intronic sequence of LMBR1.犬多趾突变在LMBR1保守内含子序列中具有异质性起源。
Genetics. 2008 Aug;179(4):2163-72. doi: 10.1534/genetics.108.087114. Epub 2008 Aug 9.
9
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.
10
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.

一个新的 13 碱基对插入在 sonic hedgehog ZRS 肢部增强子(ZRS/LMBR1)中,导致了具有三叉状拇指的前轴多指。

A novel 13 base pair insertion in the sonic hedgehog ZRS limb enhancer (ZRS/LMBR1) causes preaxial polydactyly with triphalangeal thumb.

机构信息

Department of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.

出版信息

Hum Mutat. 2012 Jul;33(7):1063-6. doi: 10.1002/humu.22097. Epub 2012 May 11.

DOI:10.1002/humu.22097
PMID:22495965
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3370115/
Abstract

Mutations in the Sonic hedgehog limb enhancer, the zone of polarizing activity regulatory sequence (ZRS, located within the gene LMBR1), commonly called the ZRS), cause limb malformations. In humans, three classes of mutations have been proposed based on the limb phenotype; single base changes throughout the region cause preaxial polydactyly (PPD), single base changes at one specific site cause Werner mesomelic syndrome, and large duplications cause polysyndactyly. This study presents a novel mutation-a small insertion. In a Swedish family with autosomal-dominant PPD, we found a 13 base pair insertion within the ZRS, NG_009240.1:g.106934_106935insTAAGGAAGTGATT (traditional nomenclature: ZRS603ins13). Computational transcription factor-binding site predictions suggest that this insertion creates new binding sites and a mouse enhancer assay shows that this insertion causes ectopic gene expression. This study is the first to discover a small insertion in an enhancer that causes a human limb malformation and suggests a potential mechanism that could explain the ectopic expression caused by this mutation.

摘要

Sonic hedgehog 肢芽增强子(位于 LMBR1 基因内的极性活动调节序列 (ZRS))中的突变通常被称为 ZRS),可导致肢体畸形。在人类中,根据肢体表型提出了三类突变;整个区域的单个碱基变化导致前轴多指(PPD),一个特定部位的单个碱基变化导致 Werner 中胚层综合征,而大片段重复则导致并指。本研究提出了一种新的突变——小插入。在一个瑞典常染色体显性 PPD 家族中,我们发现 ZRS 内有一个 13 碱基对的插入,NG_009240.1:g.106934_106935insTAAGGAAGTGATT(传统命名法:ZRS603ins13)。计算转录因子结合位点预测表明,该插入产生了新的结合位点,而小鼠增强子试验表明该插入导致异位基因表达。本研究首次发现了一个导致人类肢体畸形的增强子中的小插入,并提出了一种可能的机制,可以解释该突变引起的异位表达。