Expression of Calmodulin and Myosin Light Chain Kinase during Larval Settlement of the Barnacle Balanus amphitrite

被引:23
作者
Chen, Zhang-Fan [1 ]
Wang, Hao [1 ]
Matsumura, Kiyotaka [1 ]
Qian, Pei-Yuan [1 ]
机构
[1] Hong Kong Univ Sci & Technol, KAUST Global Collaborat Res Program, Div Life Sci, Hong Kong, Hong Kong, Peoples R China
来源
PLOS ONE | 2012年 / 7卷 / 02期
关键词
SIGNAL-TRANSDUCTION; CYPRIS LARVAE; MESSENGER-RNA; METAMORPHOSIS; GENE; PHOSPHORYLATION; PURIFICATION; INVOLVEMENT; CLONING; MODULATOR;
D O I
10.1371/journal.pone.0031337
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Barnacles are one of the most common organisms in intertidal areas. Their life cycle includes seven free-swimming larval stages and sessile juvenile and adult stages. The transition from the swimming to the sessile stages, referred to as larval settlement, is crucial for their survivor success and subsequent population distribution. In this study, we focused on the involvement of calmodulin (CaM) and its binding proteins in the larval settlement of the barnacle, Balanus (=Amphibalanus) amphitrite. The full length of CaM gene was cloned from stage II nauplii of B. amphitrite (referred to as Ba-CaM), encoding 149 amino acid residues that share a high similarity with published CaMs in other organisms. Quantitative real-time PCR showed that Ba-CaM was highly expressed in cyprids, the stage at which swimming larvae are competent to attach and undergo metamorphosis. In situ hybridization revealed that the expressed Ba-CaM gene was localized in compound eyes, posterior ganglion and cement glands, all of which may have essential functions during larval settlement. Larval settlement assays showed that both the CaM inhibitor compound 48/80 and the CaM-dependent myosin light chain kinase (MLCK) inhibitor ML-7 effectively blocked barnacle larval settlement, whereas Ca2+/CaM-dependent kinase II (CaMKII) inhibitors did not show any clear effects. The subsequent real-time PCR assay showed a higher expression level of Ba-MLCK gene in larval stages than in adults, suggesting an important role of Ba-MLCK gene in larval development and competency. Overall, the results suggest that CaM and CaM-dependent MLCK function during larval settlement of B. amphitrite.
引用
收藏
页数:9
相关论文
共 50 条
  • [31] The long myosin light chain kinase is differentially phosphorylated during interphase and mitosis
    Dulyaninova, NG
    Bresnick, AR
    [J]. EXPERIMENTAL CELL RESEARCH, 2004, 299 (02) : 303 - 314
  • [32] MicroRNA Regulation of Nonmuscle Myosin Light Chain Kinase Expression in Human Lung Endothelium
    Adyshev, Djanybek M.
    Moldobaeva, Nurgul
    Mapes, Brandon
    Elangovan, Venkate
    Garcia, Joe G. N.
    [J]. AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2013, 49 (01) : 58 - 66
  • [33] The regulatory role of arginine kinase during larval settlement of the bryozoan Bugula neritina
    Zhang, Yu
    Yang, Xiao-Xue
    Wong, Yue-Him
    Qian, Pei-Yuan
    [J]. MARINE BIOLOGY, 2018, 165 (03)
  • [34] Article Mathematical modeling and biochemical analysis support partially ordered calmodulin-myosin light chain kinase binding
    MacEwen, Melissa J. S.
    Rusnac, Domnita-Valeria
    Ermias, Henok
    Locke, Timothy M.
    Gizinski, Hayden E.
    Dexter, Joseph P.
    Sancak, Yasemin
    [J]. ISCIENCE, 2023, 26 (04)
  • [35] Phosphorylation of caldesmon by myosin light chain kinase increases its binding affinity for phosphorylated myosin filaments
    Sobieszek, Apolinary
    Sarg, Bettina
    Lindner, Herbert
    Seow, Chun Y.
    [J]. BIOLOGICAL CHEMISTRY, 2010, 391 (09) : 1091 - 1104
  • [36] Smooth muscle myosin light chain kinase efficiently phosphorylates serine 15 of cardiac myosin regulatory light chain
    Josephson, Matthew P.
    Sikkink, Laura A.
    Penheiter, Alan R.
    Burghardt, Thomas P.
    Ajtai, Katalin
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2011, 416 (3-4) : 367 - 371
  • [37] Characterization of Ca2+/calmodulin-dependent protein kinase I as a myosin II regulatory light chain kinase in vitro and in vivo
    Suizu, F
    Fukuta, Y
    Ueda, K
    Iwasaki, T
    Tokumitsu, H
    Hosoya, H
    [J]. BIOCHEMICAL JOURNAL, 2002, 367 (02) : 335 - 345
  • [38] Design of peptidase-resistant peptide inhibitors of myosin light chain kinase
    Khapchaev, Asker Y.
    Kazakova, Olga A.
    Samsonov, Mikhail V.
    Sidorova, Maria V.
    Bushuev, Valery N.
    Vilitkevich, Elena L.
    Az'muko, Andrey A.
    Molokoedov, Alexander S.
    Bespalova, Zhanna D.
    Shirinsky, Vladimir P.
    [J]. JOURNAL OF PEPTIDE SCIENCE, 2016, 22 (11-12) : 673 - 681
  • [39] Myosin Light Chain Kinase Is Necessary for Tonic Airway Smooth Muscle Contraction
    Zhang, Wen-Cheng
    Peng, Ya-Jing
    Zhang, Gen-Sheng
    He, Wei-Qi
    Qiao, Yan-Ning
    Dong, Ying-Ying
    Gao, Yun-Qian
    Chen, Chen
    Zhang, Cheng-Hai
    Li, Wen
    Shen, Hua-Hao
    Ning, Wen
    Kamm, Kristine E.
    Stull, James T.
    Gao, Xiang
    Zhu, Min-Sheng
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2010, 285 (08) : 5522 - 5531
  • [40] Albumin Causes Increased Myosin Light Chain Kinase Expression in Astrocytes Via p38 Mitogen-Activated Protein Kinase
    Rossi, Janet L.
    Ranaivo, Hantamalala Ralay
    Patel, Fatima
    Chrzaszcz, MaryAnn
    Venkatesan, Charu
    Wainwright, Mark S.
    [J]. JOURNAL OF NEUROSCIENCE RESEARCH, 2011, 89 (06) : 852 - 861