ZC3HC1 Is a Novel Inherent Component of the Nuclear Basket, Resident in a State of Reciprocal Dependence with TPR

Cells. 2021 Jul 30;10(8):1937. doi: 10.3390/cells10081937.

Abstract

The nuclear basket (NB) scaffold, a fibrillar structure anchored to the nuclear pore complex (NPC), is regarded as constructed of polypeptides of the coiled-coil dominated protein TPR to which other proteins can bind without contributing to the NB's structural integrity. Here we report vertebrate protein ZC3HC1 as a novel inherent constituent of the NB, common at the nuclear envelopes (NE) of proliferating and non-dividing, terminally differentiated cells of different morphogenetic origin. Formerly described as a protein of other functions, we instead present the NB component ZC3HC1 as a protein required for enabling distinct amounts of TPR to occur NB-appended, with such ZC3HC1-dependency applying to about half the total amount of TPR at the NEs of different somatic cell types. Furthermore, pointing to an NB structure more complex than previously anticipated, we discuss how ZC3HC1 and the ZC3HC1-dependent TPR polypeptides could enlarge the NB's functional repertoire.

Keywords: NIPA; ZC3HC1; nuclear basket; nuclear interacting partner of ALK; nuclear pore complex; nucleoprotein TPR; translocated promoter region.

MeSH terms

  • Adaptor Proteins, Signal Transducing / genetics
  • Adaptor Proteins, Signal Transducing / metabolism*
  • Animals
  • Cell Cycle Proteins / genetics
  • Cell Cycle Proteins / metabolism*
  • Female
  • HCT116 Cells
  • HeLa Cells
  • Humans
  • Macaca mulatta
  • Neoplasms / genetics
  • Neoplasms / metabolism*
  • Neoplasms / ultrastructure
  • Nuclear Pore / genetics
  • Nuclear Pore / metabolism*
  • Nuclear Pore / ultrastructure
  • Nuclear Pore Complex Proteins / genetics
  • Nuclear Pore Complex Proteins / metabolism*
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism*
  • Oocytes / metabolism*
  • Oocytes / ultrastructure
  • Protein Binding
  • Proto-Oncogene Proteins / genetics
  • Proto-Oncogene Proteins / metabolism*
  • Signal Transduction
  • Xenopus Proteins / genetics
  • Xenopus Proteins / metabolism*
  • Xenopus laevis

Substances

  • Adaptor Proteins, Signal Transducing
  • Cell Cycle Proteins
  • Nuclear Pore Complex Proteins
  • Nuclear Proteins
  • Proto-Oncogene Proteins
  • TPR protein, human
  • Xenopus Proteins
  • ZC3HC1 protein, human