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Numb and Numblike regulate sarcomere assembly and maintenance
Baolei Wang, … , Min Yang, Shujuan Li
Baolei Wang, … , Min Yang, Shujuan Li
Published February 1, 2022
Citation Information: J Clin Invest. 2022;132(3):e139420. https://doi.org/10.1172/JCI139420.
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Research Article Muscle biology

Numb and Numblike regulate sarcomere assembly and maintenance

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Abstract

A sarcomere is the contractile unit of the myofibril in striated muscles such as cardiac and skeletal muscles. The assembly of sarcomeres depends on multiple molecules that serve as raw materials and participate in the assembly process. However, the mechanism of this critical assembly process remains largely unknown. Here, we found that the cell fate determinant Numb and its homolog Numblike regulated sarcomere assembly and maintenance in striated muscles. We discovered that Numb and Numblike are sarcomeric molecules that were gradually confined to the Z-disc during striated muscle development. Conditional knockout of Numb and Numblike severely compromised sarcomere assembly and its integrity and thus caused organelle dysfunction. Notably, we identified that Numb and Numblike served as sarcomeric α-Actin–binding proteins (ABPs) and shared a conserved domain that can bind to the barbed end of sarcomeric α-Actin. In vitro fluorometric α-Actin polymerization assay showed that Numb and Numblike also played a role in the sarcomeric α-Actin polymerization process. Last, we demonstrate that Numb and Numblike regulate sarcomeric α-Actinin–dependent (ACTN-dependent) Z-disc consolidation in the sarcomere assembly and maintenance. In summary, our studies show that Numb and its homolog Numblike regulate sarcomere assembly and maintenance in striated muscles, and demonstrate a molecular mechanism by which Numb/Numblike, sarcomeric α-Actin, and ACTN cooperate to control thin filament formation and Z-disc consolidation.

Authors

Baolei Wang, Min Yang, Shujuan Li

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Figure 5

Numb and Numblike regulate Z-disc assembly and integrity through ACTN.

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Numb and Numblike regulate Z-disc assembly and integrity through ACTN.
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(A) Double immunofluorescence staining of Numb and ACTN in the CMs of E14.5 CTL and MLC-2v-cre DKO mice after 72-hour culture in vitro (ACTN, green; Numb, red; original magnification, ×630, zoom in ×2; amplified images: original magnification, ×630, zoom in ×5). (B) Double immunofluorescence staining of Numb and ACTN in the SKMs of CKMM-cre DKO mice on P60.5 (ACTN, green; Numb, red; original magnification, ×630, zoom in ×2). (C) Coimmunoprecipitation of N-WASP with other ABPs in heart and SKM lysates of CTL and CKMM-cre DKO mice on P60.5. (D and E) Relative protein level of ABPs immunoprecipitated by N-WASP in heart and SKM lysates of CTL and CKMM-cre DKO mice on P60 (n = 3). (F) Coimmunoprecipitation of α-Actin (ACTC1) with ACTN in heart lysates of CTL and α-MHC-cre DKO mice on P60.5. (G) Relative ACTN protein level immunoprecipitated by ACTC1 in heart lysates of CTL and α-MHC-Cre DKO mice on P60.5 (n = 4). Scale bars: 5 μm. Two-tailed Student’s t test with error bars showing mean ± SD.

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