Kim H-W, Chang E S, Mykles D L
Department of Biology, Colorado State University, Fort Collins, CO 80523, USA.
J Exp Biol. 2005 Aug;208(Pt 16):3177-97. doi: 10.1242/jeb.01754.
Crustacean muscle has four calpain-like proteinase activities (CDP I, IIa, IIb and III) that are involved in molt-induced claw muscle atrophy, as they degrade myofibrillar proteins in vitro and in situ. Using PCR cloning techniques, three full-length calpain cDNAs (Gl-CalpB, Gl-CalpM and Gl-CalpT) were isolated from limb regenerates of the tropical land crab Gecarcinus lateralis. All three had highly conserved catalytic (dII) and C2-like (dIII) domains. Gl-CalpB was classified as a typical, or EF-hand, calpain, as the deduced amino acid sequence had a calmodulin-like domain IV in the C-terminus and was most similar to Drosophila calpains A and B. Based on its estimated mass (approximately 88.9 kDa) and cross-immunoreactivity with a polyclonal antibody raised against Dm-CalpA, Gl-CalpB may encode CDP IIb, which is a homodimer of a 95-kDa subunit. It was expressed in all tissues examined, including skeletal muscle, heart, integument, gill, digestive gland, hindgut, nerve ganglia, gonads and Y-organ (molting gland). Both Gl-CalpM and Gl-CalpT were classified as atypical, or non-EF-hand, calpains, as they lacked a domain IV sequence. Gl-CalpM was a homolog of Ha-CalpM from lobster, based on similarities in deduced amino acid sequence, estimated mass (approximately 65.2 kDa) and structural organization (both were truncated at the C-terminal end of dIII). It was expressed at varying levels in most tissues, except Y-organ. Gl-CalpT (approximately 74.6 kDa) was similar to TRA-3 in the nematode Caenorhabditis elegans; domain IV was replaced by a unique ;T domain' sequence. It was expressed in most tissues, except eyestalk ganglia and Y-organ. The effects of elevated ecdysteroid, induced by eyestalk ablation, on calpain and ecdysone receptor (Gl-EcR) mRNA levels in skeletal muscles were quantified by real-time PCR. At 1 day after eyestalk ablation, Gl-EcR and Gl-CalpT mRNA levels increased 15- and 19.3-fold, respectively, in claw muscle but not in thoracic muscle. At 3 days after eyestalk ablation, Gl-EcR and Gl-CalpT mRNA levels in claw muscle had decreased to 2.8-fold and 4.3-fold higher than those in intact controls, respectively, suggesting a feedback inhibition by ecdysteroid. There was no significant effect of eyestalk ablation on Gl-CalpB and Gl-CalpM mRNA levels. Gl-CalpT and Gl-EcR mRNA levels were significantly correlated in both claw and thoracic muscles from intact and eyestalk-ablated animals. The data suggest that Gl-CalpT is involved in initiation of claw muscle atrophy by ecdysteroids. Premolt reduction in claw muscle mass and concomitant remodeling of the sarcomere probably result from post-transcriptional regulation of calpains.
甲壳类动物肌肉具有四种钙蛋白酶样蛋白酶活性(CDP I、IIa、IIb和III),它们参与蜕皮诱导的爪肌萎缩,因为它们在体外和原位降解肌原纤维蛋白。利用PCR克隆技术,从热带陆地蟹Gecarcinus lateralis的肢体再生组织中分离出三个全长钙蛋白酶cDNA(Gl-CalpB、Gl-CalpM和Gl-CalpT)。这三种钙蛋白酶都具有高度保守的催化结构域(dII)和C2样结构域(dIII)。Gl-CalpB被归类为典型的或EF-手型钙蛋白酶,因为推导的氨基酸序列在C端有一个钙调蛋白样结构域IV,并且与果蝇钙蛋白酶A和B最相似。根据其估计质量(约88.9 kDa)以及与针对Dm-CalpA产生的多克隆抗体的交叉免疫反应性,Gl-CalpB可能编码CDP IIb,它是一个95-kDa亚基的同二聚体。它在所有检测的组织中都有表达,包括骨骼肌、心脏、表皮、鳃、消化腺、后肠、神经节、性腺和Y器官(蜕皮腺)。Gl-CalpM和Gl-CalpT都被归类为非典型的或非EF-手型钙蛋白酶,因为它们缺乏结构域IV序列。基于推导的氨基酸序列、估计质量(约65.2 kDa)和结构组织的相似性(两者在dIII的C末端都被截断),Gl-CalpM是龙虾Ha-CalpM的同源物。它在大多数组织中以不同水平表达,Y器官除外。Gl-CalpT(约74.6 kDa)与秀丽隐杆线虫中的TRA-3相似;结构域IV被一个独特的“T结构域”序列取代。它在大多数组织中表达,眼柄神经节和Y器官除外。通过实时PCR定量了眼柄切除诱导的蜕皮类固醇升高对骨骼肌中钙蛋白酶和蜕皮激素受体(Gl-EcR)mRNA水平的影响。眼柄切除后1天,爪肌中Gl-EcR和Gl-CalpT mRNA水平分别增加了15倍和19.3倍,而胸肌中没有增加。眼柄切除后3天,爪肌中Gl-EcR和Gl-CalpT mRNA水平分别降至比完整对照组高2.8倍和4.3倍,表明蜕皮类固醇存在反馈抑制。眼柄切除对Gl-CalpB和Gl-CalpM mRNA水平没有显著影响。在完整和眼柄切除动物的爪肌和胸肌中,Gl-CalpT和Gl-EcR mRNA水平都显著相关。数据表明,Gl-CalpT参与蜕皮类固醇诱导的爪肌萎缩的起始过程。蜕皮前爪肌质量的减少和肌节的伴随重塑可能是由于钙蛋白酶的转录后调控。