Zhang Zhen, Duan Yanyu, Wu Zhongping, Zhang Hui, Ren Jun, Huang Lusheng
State Key Laboratory of Pig Genetic Improvement and Production Technology, Jiangxi Agricultural University, Nanchang, 330045, China.
Int J Biol Sci. 2017 May 16;13(5):669-681. doi: 10.7150/ijbs.19714. eCollection 2017.
Peroxisome proliferator-activated receptor beta/delta (PPARD) is an important determinant of multiple biological processes. Our previous studies identified a missense mutation in the gene that significantly reduces its transcription activity, and consequently causes enlarged external ears in pigs. However, the mechanisms underlying the causality has remained largely unknown. Here, we show that PPARD retards the development of auricular cartilage by accelerating the apoptosis of cartilage stem/progenitor cells (CSPCs), the terminal differentiation of cartilage cells and the degradation of cartilage extracellular matrix in the auricle. At the transcription level, PPARD upregulates a set of genes that are associated with CSPCs apoptosis and chondrogenic differentiation, chondroblast differentiation and extracellular matrix degradation. ChIP-seq identified direct target genes of PPARD, including a well-documented gene for cartilage development: . We further show that compared to wild-type PPARD, the G32E mutant up-regulates the expression of and subsequently leads to the downregulation of critical genes that inhibit cartilage growth. These findings allow us to conclude that PPARD is an inhibitor of auricular cartilage growth in pigs. The causative mutation (G32E) in the gene attenuates the PPARD-mediated retardation of cartilage growth in the auricle, contributing to enlarged ears in pigs. The findings advance our understanding of the mechanisms underlying auricular development in mammals, and shed insight into the studies of innate pinna disorders and cartilage regeneration medicine in humans.
过氧化物酶体增殖物激活受体β/δ(PPARD)是多种生物学过程的重要决定因素。我们之前的研究在该基因中鉴定出一个错义突变,该突变显著降低其转录活性,从而导致猪的耳朵增大。然而,这种因果关系背后的机制在很大程度上仍然未知。在此,我们表明PPARD通过加速软骨干/祖细胞(CSPCs)的凋亡、软骨细胞的终末分化以及耳廓软骨细胞外基质的降解来延缓耳廓软骨的发育。在转录水平上,PPARD上调了一组与CSPCs凋亡和软骨生成分化、成软骨细胞分化以及细胞外基质降解相关的基因。ChIP-seq鉴定出PPARD的直接靶基因,包括一个已充分证明与软骨发育相关的基因: 。我们进一步表明,与野生型PPARD相比,G32E突变体上调了 的表达,随后导致抑制软骨生长的关键基因下调。这些发现使我们得出结论,PPARD是猪耳廓软骨生长的抑制剂。该基因中的致病突变(G32E)减弱了PPARD介导的耳廓软骨生长延迟,导致猪耳朵增大。这些发现推进了我们对哺乳动物耳廓发育机制的理解,并为人类先天性耳廓疾病和软骨再生医学的研究提供了见解。