首页> 外文期刊>American journal of medical genetics, Part A >Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36.
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Genetic heterogeneity in type III familial cutaneous syndactyly and linkage to chromosome 7q36.

机译:III型家族皮肤的遗传异质性与染色体7q36连锁。

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摘要

The ZRS (zone of polarizing activity regulatory sequence) is a long-range limb-specific Sonic Hedgehog (SHH) enhancer. In humans, the ZRS is located in chromosome 7q36 within intron 5 of LMBR1; approximately 1 Mb telomeric of SHH. Point mutations and duplications of the ZRS lead to a variable phenotype of preaxial polydactyly/triphalangeal thumb, tibial hypoplasia, radial ray deficiency, and type IV familial syndactyly (syndactyly of all digits with polydactyly). The ZRS is conserved among mammals and fish and regulates the expression of SHH. In mice, the conserved ZRS within the Lmbr1 gene is found in chromosome 5. The Hammertoe (Hm) mouse mutants have a mutation in the Lmbr1 locus and show syndactyly of digits 2-5 without polydactyly. No previous reports have described isolated syndactyly without polydactyly to be related to the LMBR1 locus in humans. In this report, we describe a family with simple cutaneous syndactyly involving digits 2-5, without polydactyly which is consistent with the phenotype of type III syndactyly. The locus we identified on ch7q36.3 is syntenic to the Hm locus; and affected members of the family had a phenotype analogous to Hm. Hence, the type of syndactyly described in the current report may be equivalent to Hm mice.
机译:ZRS(极化活性调节序列区)是一种远程肢体特异性Sonic Hedgehog(SHH)增强剂。在人类中,ZRS位于LMBR1内含子5内的7q36染色体上。大约1 Mb SHH端粒。 ZRS的点突变和重复会导致前轴多指/三趾拇指,胫骨发育不全,radial骨射线缺乏和IV型家族性综合征(所有数字同指多指)的可变表型。 ZRS在哺乳动物和鱼类中是保守的,并调节SHH的表达。在小鼠中,Lmbr1基因内的保守ZRS在第5号染色体上发现。Hammertoe(Hm)小鼠突变体在Lmbr1基因座中具有突变,并显示2-5位的合子,而没有多义性。没有先前的报道描述过分离地无人多指地与人类的LMBR1基因座相关。在这份报告中,我们描述了一个家庭,其皮肤上涉及2-5位数的简单皮肤,而没有与3型表型相同的多指。我们在ch7q36.3上确定的基因座与Hm基因座是同义的。受影响家庭的表型与Hm类似。因此,本报告中描述的综合征类型可能等同于Hm小鼠。

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