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HAND2 基因剂量过高会导致人类染色体部分三体综合征 4q 远端肢体和心脏缺陷。

Overdosage of Hand2 causes limb and heart defects in the human chromosomal disorder partial trisomy distal 4q.

机构信息

Genetic Strains Research Center, Mammalian Genetics Laboratory, National Institute of Genetics, 1111 Yata, Mishima, Shizuoka 411-8540, Japan.

出版信息

Hum Mol Genet. 2013 Jun 15;22(12):2471-81. doi: 10.1093/hmg/ddt099. Epub 2013 Feb 27.

Abstract

Partial trisomy distal 4q (denoted 4q+) is a human chromosomal disorder caused by duplication of the distal end of the long arm of chromosome 4 (Chr4). This disorder manifests typical phenotypes, including craniofacial, renal, heart and thumb developmental defects. Although these clinical features are likely caused by a dosage imbalance in the gene network involving the trisomic region, the causative gene or genes and the molecular bases are largely unknown. Here, we report mouse Recombination-induced mutation 4 (Rim4) as a model animal of 4q+. The Rim4 genome contains an insertion of a 6.5 Mb fragment from mouse chromosome 8 into chromosome 6. This insertion fragment contains 17 genes, including Hand2, that encode the basic helix-loop-helix transcription factor and is syntenic to the distal end of human Chr4, 4q32.3 to 4q34.1, which is responsible for 4q+. A comparison of phenotypes between patients with Rim4 and 4q+ revealed that Rim4 shows direct parallels with many phenotypes of 4q+ such as craniofacial, heart, cervical vertebra and limb deformities. Rebalancing the gene dosage by a genetic cross with Hand2 knockout mice ameliorated symptoms of the heart and limb deformities of Rim4. Conversely, an increase in copy number of Hand2 in wild-type mice recaptures the heart and limb deformities of Rim4. Our results collectively demonstrate that overdosage of Hand2 is a major cause for at least the limb and heart phenotypes of 4q+ and that mouse Rim4 provides a unique animal model for understanding the molecular bases underlying the complex phenotypes of 4q+.

摘要

部分 4 号染色体长臂远端三体(表示为 4q+)是一种人类染色体疾病,由 4 号染色体(Chr4)长臂末端的重复引起。该疾病表现出典型的表型,包括颅面、肾脏、心脏和拇指发育缺陷。尽管这些临床特征可能是由于涉及三体区域的基因网络中的剂量不平衡引起的,但致病基因或基因以及分子基础在很大程度上仍是未知的。在这里,我们报告了小鼠重组诱导突变 4(Rim4)作为 4q+的模型动物。Rim4 的基因组包含一个从小鼠染色体 8 插入到染色体 6 的 6.5 Mb 片段。该插入片段包含 17 个基因,包括编码基本螺旋-环-螺旋转录因子的 Hand2,与人类 Chr4 的远端 4q32.3 到 4q34.1 同系,负责 4q+。Rim4 与 4q+患者表型的比较表明,Rim4 与许多 4q+表型直接相似,如颅面、心脏、颈椎和肢体畸形。通过与 Hand2 敲除小鼠的遗传杂交来平衡基因剂量可以改善 Rim4 的心脏和肢体畸形症状。相反,在野生型小鼠中增加 Hand2 的拷贝数可以重现 Rim4 的心脏和肢体畸形。我们的结果共同表明,Hand2 的过度表达是至少引起 4q+肢体和心脏表型的主要原因,并且小鼠 Rim4 为理解 4q+复杂表型的分子基础提供了一个独特的动物模型。

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