Laboratory of Cellular and Molecular Biotechnology, Faculty of Science, Kochi University, Kochi 780-8520, Japan.
Dev Biol. 2012 Aug 15;368(2):393-403. doi: 10.1016/j.ydbio.2012.06.006. Epub 2012 Jun 12.
A homolog of receptor for activated protein kinase C1 (RACK1) was cloned from the budding tunicate Polyandrocarpa misakiensis. By RT-PCR and in situ hybridization analyses, PmRACK1 showed biphasic gene expression during asexual and sexual reproduction. In developing buds, the signal was exclusively observed in the multipotent atrial epithelium and undifferentiated mesenchymal cells that contributed to morphogenesis by the mesenchymal-epithelial transition (MET). In juvenile zooids, the signal was first observable in germline precursor cells that arose as mesenchymal cell aggregated in the ventral hemocoel. In mature zooids, the germinal epithelium in the ovary and the pharynx were the most heavily stained parts. GFP reporter assay indicated that the ovarian expression of PmRACK1 was constitutive from germline precursor cells to oocytes. To elucidate the in vivo function of PmRACK1, RNA interference was challenged. When growing buds were incubated with 5 nmol/mL siRNA, most mesenchymal cells remained round and appeared to have no interactions with the extracellular matrix (ECM), causing lower activity of MET without any apparent effects on cell proliferation. The resultant zooids became growth-deficient. The dwarf zooids did not form buds or mature gonads. Prior to RNAi, buds were treated with human BMP4 that could induce PmRACK1 expression, which resulted in MET activity. We conclude that in P. misakiensis, PmRACK1 plays roles in mesenchymal cell recruitment during formation of somatic and gonad tissues, which contributes to zooidal growth and sexual and asexual reproduction.
从芽胞被囊动物多瘤海鞘 Polyandrocarpa misakiensis 中克隆出了激活蛋白激酶 C1 受体(RACK1)的同源物。通过 RT-PCR 和原位杂交分析,PmRACK1 在无性和有性生殖过程中表现出两相基因表达。在发育中的芽中,信号仅在多能性心房上皮细胞和未分化的间充质细胞中观察到,这些细胞通过间质-上皮转化(MET)为形态发生做出贡献。在幼体浮游生物中,信号首先在生殖细胞前体细胞中观察到,这些细胞是在腹侧血腔中聚集的间充质细胞产生的。在成熟的浮游生物中,卵巢和咽部的生殖上皮是染色最深的部分。GFP 报告基因分析表明,PmRACK1 的卵巢表达从生殖细胞前体细胞到卵母细胞是组成型的。为了阐明 PmRACK1 的体内功能,进行了 RNA 干扰挑战。当生长的芽与 5 nmol/mL siRNA 孵育时,大多数间充质细胞保持圆形,似乎与细胞外基质(ECM)没有相互作用,导致 MET 活性降低,而对细胞增殖没有任何明显影响。由此产生的浮游生物生长不足。矮小的浮游生物不能形成芽或成熟的性腺。在 RNAi 之前,用人类 BMP4 处理芽,BMP4 可以诱导 PmRACK1 的表达,从而导致 MET 活性。我们得出结论,在多瘤海鞘中,PmRACK1 在形成体细胞和性腺组织的间充质细胞募集中发挥作用,这有助于浮游生物的生长和有性和无性繁殖。