FEBS Open Bio (Aug 2021)

Expression and cell transformation activity of dynactin‐associated protein isoforms

  • Xiaobo Yin,
  • Shota Yamada,
  • Hiroaki Kobayashi,
  • Ryota Tanaka,
  • Yuki Togo,
  • Miho Hosoi,
  • Mie Tsuchida,
  • Tatsuki Kunoh,
  • Shuichi Wada,
  • Toshinobu Nakamura,
  • Ryuzo Sasaki,
  • Tamio Mizukami,
  • Makoto Hasegawa

DOI
https://doi.org/10.1002/2211-5463.13202
Journal volume & issue
Vol. 11, no. 8
pp. 2110 – 2117

Abstract

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Overexpression of human dynactin‐associated protein isoform a (dynAPa) transforms NIH3T3 cells. DynAPa is a single‐pass transmembrane protein with a carboxy‐terminal region exposed to the outside of cells. According to the NCBI RefSeq database, there may be two other splicing variants of the encoding gene (dynAPb and c). DynAPa and c differ in some amino‐terminal residues (NH2‐MVA in dynAPa and NH2‐MEYQLL in dynAPc). DynAPb has the same amino‐terminal residues as dynAPc, but lacks 55 residues in the intracellular region. All three isoforms have the same carboxy‐terminal region, including the transmembrane domain. Expression of mRNAs of three splicing variants was found in human cancer cell lines ACHN and Caki‐1. The subcellular localization and in vitro cell transformation ability of the three isoforms were examined using NIH3T3 cells overexpressing each respective isoform. All isoforms were found to be localized to the Golgi apparatus and plasma membrane, where the carboxy‐terminal region was exposed to the outside of cells. Cell transformation was tested using focus formation due to loss of contact inhibition of cell proliferation, and colony formation was examined on soft agar and spheroid formation in ultralow U‐bottomed wells. DynAPa robustly formed foci and colonies on soft agar and spheroid, whereas these abilities were considerably decreased for dynAPb and completely lost in dynAPc. These findings warrant dissection studies to identify the dynAP domain that is required for cell transformation.

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