Hammer J A, Jung G, Korn E D
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4655-9. doi: 10.1073/pnas.83.13.4655.
Acanthamoeba castellanii contains two enzymes, myosins IA and IB, that exhibit the catalytic properties of a myosin but possess very unusual physical properties, the most striking of which are their single, low molecular weight heavy chain, their globular shape, and their inability to form bipolar filaments. We have now isolated a putative myosin IB heavy chain gene from Acanthamoeba, using as a heterologous probe a portion of a sarcomeric myosin heavy chain gene from Caenorhabditis elegans. The amoeba genomic clone hybridizes to a 4250-nucleotide RNA species and hybrid-selects an mRNA encoding a 125-kDa polypeptide. This polypeptide comigrates exactly with the heavy chain of purified amoeba myosin IB and is specifically immunoprecipitated with antiserum to myosin IB. We sequenced two restriction enzyme fragments of this gene, and the deduced amino acid sequences show strong homology with the regions of muscle myosins that contain the reactive thiols and the ATP binding site. Our identification of a myosin IB heavy chain gene demonstrates that myosin IB, despite the unusually low molecular weight of its heavy chain, is a true gene product. The sequence results show that, despite its atypical physical properties, myosin IB is clearly related to conventional myosins.
卡氏棘阿米巴含有两种酶,肌球蛋白IA和IB,它们表现出肌球蛋白的催化特性,但具有非常不寻常的物理特性,其中最显著的是它们单一的低分子量重链、球状形状以及无法形成双极丝。我们现在从卡氏棘阿米巴中分离出了一个假定的肌球蛋白IB重链基因,使用秀丽隐杆线虫肌节肌球蛋白重链基因的一部分作为异源探针。该阿米巴基因组克隆与一种4250个核苷酸的RNA物种杂交,并杂交选择出一种编码125 kDa多肽的mRNA。这种多肽与纯化的阿米巴肌球蛋白IB的重链完全共迁移,并且被抗肌球蛋白IB的抗血清特异性免疫沉淀。我们对该基因的两个限制性酶切片段进行了测序,推导的氨基酸序列与肌肉肌球蛋白中含有反应性巯基和ATP结合位点的区域具有很强的同源性。我们对肌球蛋白IB重链基因的鉴定表明,尽管肌球蛋白IB的重链分子量异常低,但它是一个真正的基因产物。序列结果表明,尽管肌球蛋白IB具有非典型的物理特性,但它与传统肌球蛋白明显相关。