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C型利钠肽与过度生长

C-type natriuretic peptide and overgrowth.

作者信息

Bocciardi Renata, Ravazzolo Roberto

机构信息

Laboratory of Molecular Genetics, G. Gaslini Institute, Genova, Italy.

出版信息

Endocr Dev. 2009;14:61-6. doi: 10.1159/000207477. Epub 2009 Feb 27.

Abstract

Natriuretic peptides are a family of structurally related peptides with different distinct biological effects. C-type natriuretic peptide (CNP)-mediated signaling is important for endochondral ossification and intervenes in the control of chondrocyte maturation by regulating the balance between proliferation and terminal differentiation. CNP is encoded by the NPPC gene on human chromosome 2 for which, so far, no mutations have been described in humans. Recently, two independent articles reported the description of 3 patients with a similar clinical phenotype characterized by the presence of skeletal anomalies and overgrowth. In all 3 cases, the clinical picture was associated with the presence of a balanced translocation involving chromosome 2 and causing overexpression of the NPPC gene and an increased plasma concentration of its product, CNP. Transcriptional dysregulation of NPPC has been ascribed to the separation of the gene unit from the long-range regulatory element with a transcriptional silencing effect on its expression and CNP overproduction has been correlated to the skeletal overgrowth phenotype observed.

摘要

利钠肽是一组结构相关的肽类,具有不同的独特生物学效应。C型利钠肽(CNP)介导的信号传导对于软骨内成骨很重要,并通过调节增殖与终末分化之间的平衡来干预软骨细胞成熟的控制。CNP由人类2号染色体上的NPPC基因编码,迄今为止,尚未在人类中描述该基因的突变。最近,两篇独立的文章报道了3例具有相似临床表型的患者,其特征为存在骨骼异常和过度生长。在所有3例病例中,临床表现均与涉及2号染色体的平衡易位有关,该易位导致NPPC基因过表达及其产物CNP的血浆浓度升高。NPPC的转录失调归因于基因单位与远距离调节元件的分离,对其表达具有转录沉默作用,并且CNP的过量产生与观察到的骨骼过度生长表型相关。

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