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非洲爪蟾ADF/丝切蛋白磷酸酶(弹弓蛋白,XSSH)的同源物在原肠胚形成运动中的功能作用。

Functional involvement of Xenopus homologue of ADF/cofilin phosphatase, slingshot (XSSH), in the gastrulation movement.

作者信息

Tanaka Kenji, Nishio Reina, Haneda Kaku, Abe Hiroshi

机构信息

Department of Biology, Chiba University, Japan.

出版信息

Zoolog Sci. 2005 Sep;22(9):955-69. doi: 10.2108/zsj.22.955.

Abstract

ADF/cofilin is a phosphorylation-regulated protein essential for actin filament dynamics in cells. Here, we cloned two cDNAs encoding Xenopus ADF/cofilin (XAC)-specific phosphatase, slingshot (XSSH), one of which contains an extra 15 nucleotides in a coding sequence of the other, possibly generated by alternative splicing. Whole mount in situ hybridization showed XSSH transcripts in the blastopore lip and sensorial ectoderm at stage 11, and subsequently localized to developing brain, branchial arches, developing retina, otic vesicle, cement gland, and spinal chord in neurula to tailbud embryos. Immunostaining of animal-vegetal sections of gastrula embryos demonstrated that both XAC and XSSH proteins are predominant in ectodermal and involuting mesodermal cells. Microinjection of either a wild type (thus induces overexpression) or a phosphatase-defective mutant (functions as dominantly negative form) resulted in defects in gastrulation, and often generated the spina bifida phenotype with reduced head structures. Interestingly, the ratio of phosphorylated XAC to dephosphorylated XAC markedly increased from the early gastrula stage (stage 10.5), although the amount of XSSH protein markedly increased from this stage. These results suggest that gastrulation movement requires ADF/cofilin activity through dynamic regulation of its phosphorylation state.

摘要

ADF/丝切蛋白是一种受磷酸化调节的蛋白质,对细胞中肌动蛋白丝的动态变化至关重要。在此,我们克隆了两个编码非洲爪蟾ADF/丝切蛋白(XAC)特异性磷酸酶弹弓蛋白(XSSH)的cDNA,其中一个在另一个的编码序列中含有额外的15个核苷酸,可能是通过可变剪接产生的。整体原位杂交显示,在第11阶段,XSSH转录本存在于胚孔唇和感觉外胚层中,随后在神经胚至尾芽胚胎中定位于发育中的脑、鳃弓、发育中的视网膜、耳泡、黏液腺和脊髓。对原肠胚动物-植物切片的免疫染色表明,XAC和XSSH蛋白在表皮和内卷中胚层细胞中占主导地位。显微注射野生型(从而诱导过表达)或磷酸酶缺陷型突变体(起显性负性作用)均导致原肠胚形成缺陷,并经常产生头部结构减少的脊柱裂表型。有趣的是,尽管XSSH蛋白的量从早期原肠胚阶段(第10.5阶段)开始显著增加,但磷酸化XAC与去磷酸化XAC的比例从该阶段开始显著增加。这些结果表明,原肠胚形成运动需要通过动态调节ADF/丝切蛋白的磷酸化状态来发挥其活性。

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