New N-RAP-binding partners α-actinin, filamin and Krp1 detected by yeast two-hybrid screening: implications for myofibril assembly

N-RAP, a muscle-specific protein concentrated at myotendinous junctions in skeletal muscle and intercalated disks in cardiac muscle, has been implicated in myofibril assembly. To discover more about the role of N-RAP in myofibril assembly, we used the yeast two-hybrid system to screen a mouse skeletal muscle cDNA library for proteins capable of binding N-RAP in a eukaryotic cell. From yeast two-hybrid experiments we were able to identify three new N-RAP binding partners: α-actinin, filamin-2, and Krp1 (also called sarcosin). In vitro binding assays were used to verify these interactions and to identify the N-RAP domains involved. Three regions of N-RAP were expressed as His-tagged recombinant proteins, including the nebulin-like super repeat region (N-RAP-SR), the N-terminal LIM domain (N-RAP-LIM), and the region of N-RAP in between the super repeat region and the LIM domain (N-RAP-IB). We detected significant α-actinin binding to N-RAP-IB and N-RAP-LIM, filamin binding to N-RAP-SR, and Krp1 binding to N-RAP-SR and N-RAP-IB. During myofibril assembly in cultured chick cardiomyocytes, N-RAP and filamin appear to co-localize with α-actinin in the earliest myofibril precursors found near the cell periphery, as well as in the nascent myofibrils that form as these structures fuse laterally. In contrast, Krp1 is not localized until late in the assembly process, when it appears at the periphery of myofibrils that appear to be fusing laterally. The results suggest that sequential recruitment of N-RAP binding partners may serve an important role during myofibril assembly.

[1]  A. P. Soler,et al.  Interaction of alpha-actinin with the cadherin/catenin cell-cell adhesion complex via alpha-catenin , 1995, The Journal of cell biology.

[2]  C. Moncman,et al.  Nebulette: a 107 kD nebulin-like protein in cardiac muscle. , 1995, Cell motility and the cytoskeleton.

[3]  S. Fields,et al.  Analyzing protein-protein interactions using two-hybrid system. , 1995, Methods in enzymology.

[4]  K. Johnson,et al.  Characterization of the interactions of alpha-catenin with alpha-actinin and beta-catenin/plakoglobin. , 1997, Journal of cell science.

[5]  L. Kunkel,et al.  Cloning and Characterization of Two Human Skeletal Muscle 0-actinin Genes Located on Chromosomes 1 and 11* , 2022 .

[6]  F. Protasi,et al.  Independent assembly of 1.6 microns long bipolar MHC filaments and I-Z-I bodies. , 1997, Cell structure and function.

[7]  S. Kanner,et al.  Filamin binds to the cytoplasmic domain of the beta1-integrin. Identification of amino acids responsible for this interaction. , 1998, The Journal of biological chemistry.

[8]  J. Sanger,et al.  Myofibrillogenesis visualized in living embryonic cardiomyocytes. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[9]  J. Sanger,et al.  Binding and distribution of fluorescently labeled filamin in permeabilized and living cells. , 1987, Cell motility and the cytoskeleton.

[10]  V. Koteliansky,et al.  The role of actin-binding proteins vinculin, filamin, and fibronectin in intracellular and intercellular linkages in cardiac muscle. , 1985, Advances in myocardiology.

[11]  K. Burridge,et al.  An interaction between alpha-actinin and the beta 1 integrin subunit in vitro , 1990, The Journal of cell biology.

[12]  T. Yatskievych,et al.  Assembly of thick, thin, and titin filaments in chick precardiac explants , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.

[13]  J. Sanger,et al.  The premyofibril: evidence for its role in myofibrillogenesis. , 1994, Cell motility and the cytoskeleton.

[14]  R. Horowits,et al.  Molecular interactions of N-RAP, a nebulin-related protein of striated muscle myotendon junctions and intercalated disks. , 1999, Biochemistry.

[15]  D. V. Vander Woude,et al.  Differential expression of the actin-binding proteins, alpha-actinin-2 and -3, in different species: implications for the evolution of functional redundancy. , 2001, Human molecular genetics.

[16]  R. Gomer,et al.  Different temporal patterns of expression result in the same type, amount, and distribution of filamin (ABP) in cardiac and skeletal myofibrils. , 1994, Cell motility and the cytoskeleton.

[17]  W. Goldmann,et al.  Kinetic determination of focal adhesion protein formation. , 2000, Biochemical and biophysical research communications.

[18]  K. Linask,et al.  N-cadherin is required for the differentiation and initial myofibrillogenesis of chick cardiomyocytes. , 1998, Cell motility and the cytoskeleton.

[19]  J. Zhang,et al.  Ultrastructural and biochemical localization of N-RAP at the interface between myofibrils and intercalated disks in the mouse heart. , 2001, Biochemistry.

[20]  D. Law,et al.  Terminal regions of mouse nebulin: sequence analysis and complementary localization with N-RAP. , 2000, Cell motility and the cytoskeleton.

[21]  Z. Xie,et al.  Molecular cloning of human ABPL, an actin-binding protein homologue. , 1998, Biochemical and biophysical research communications.

[22]  S. Sadiev,et al.  DNA sequence and muscle-specific expression of human sarcosin transcripts , 1998, Molecular and Cellular Biochemistry.

[23]  M. Gautel,et al.  Characterization of muscle filamin isoforms suggests a possible role of gamma-filamin/ABP-L in sarcomeric Z-disc formation. , 2000, Cell motility and the cytoskeleton.

[24]  M. Stromer,et al.  Immunocytochemistry of the muscle cell cytoskeleton , 1995, Microscopy research and technique.

[25]  J. Zhang,et al.  Complete cDNA sequence and tissue localization of N-RAP, a novel nebulin-related protein of striated muscle. , 1997, Cell motility and the cytoskeleton.

[26]  B. Ozanne,et al.  Krp1, a novel kelch related protein that is involved in pseudopod elongation in transformed cells , 2000, Oncogene.

[27]  R. Horowits,et al.  Targeting and functional role of N-RAP, a nebulin-related LIM protein, during myofibril assembly in cultured chick cardiomyocytes. , 2001, Journal of cell science.

[28]  Simon C Watkins,et al.  Filamin 2 (FLN2): A Muscle-specific Sarcoglycan Interacting Protein , 2000 .

[29]  T Masaki,et al.  Differential distribution of subsets of myofibrillar proteins in cardiac nonstriated and striated myofibrils , 1990, The Journal of cell biology.

[30]  P. Bechtel Identification of a high molecular weight actin-binding protein in skeletal muscle. , 1979, The Journal of biological chemistry.

[31]  张哉根,et al.  Leu-M , 1991 .

[32]  J C Perriard,et al.  Myofibrillogenesis in the developing chicken heart: assembly of Z-disk, M-line and the thick filaments. , 1999, Journal of cell science.

[33]  C. Moncman,et al.  Functional dissection of nebulette demonstrates actin binding of nebulin-like repeats and Z-line targeting of SH3 and linker domains. , 1999, Cell motility and the cytoskeleton.

[34]  D. Erle,et al.  Integrin β Cytoplasmic Domains Differentially Bind to Cytoskeletal Proteins* , 1998, The Journal of Biological Chemistry.

[35]  R. Kemler From cadherins to catenins: cytoplasmic protein interactions and regulation of cell adhesion. , 1993, Trends in genetics : TIG.

[36]  S. Kempa,et al.  Indications for a Novel Muscular Dystrophy Pathway , 2000, Journal of Cell Biology.

[37]  P. Caroni,et al.  Alterations at the Intercalated Disk Associated with the Absence of Muscle Lim Protein , 2001, The Journal of cell biology.

[38]  L. Cooley,et al.  The kelch repeat superfamily of proteins: propellers of cell function. , 2000, Trends in cell biology.