Characterization and potential function of a novel testis-specific nucleoporin BS-63

Mol Reprod Dev. 2002 Jan;61(1):126-34. doi: 10.1002/mrd.1139.

Abstract

A 1933 bp cDNA fragment, coding a truncated testis-specific novel nucleoporin, was isolated from a human testis lambdaZAPII cDNA library, designated as BS-63 and assigned GenBank accession number: U64675. By applying the methods of rapid amplification of cDNA ends (5' RACE) and PCR, a full-length BS-63 cDNA composed of 5475 bp was obtained. BS-63 cDNA contained an open reading frame consisting of 1765 codons and XFXFG or GLFG repetitive sequence motifs. These repetitive motifs are structural characteristic of nucleoporins. BS-63 cDNA has high homology with Nup358/Ran BP2. A 1599 bp fragment, corresponding to the C-terminus of BS-63 cDNA, was prepared and expressed in E. coli BL21(DE3). The recombinant product was purified by affinity chromatography and SDS-PAGE and polyclonal antibodies raised. In rat testis section, the BS-63 protein was localized at the sites of nuclear pores in spermatids by immuno-gold transmission electron microscopy and on the nuclear membrane of Triton X-treated sperm by colloidal silver immuno-gold scanning electron microscopy. The recombinant BS-63 protein can be phosphorylated in vitro with PKC and p34(cdc2). A yeast two-hybrid system was used to screen a mouse testis cDNA library to identify proteins capable of interacting with BS-63. Using the 1.6 kb cDNA fragment as bait, the following interacting proteins were identified: Ran, transportin (karyopherin beta2), two proteins related to the nucleocytoplasmic transporter and aF10 protein. The latter protein is a putative transcriptor containing a cysteine-rich N-terminus, a LAP/PHD finger, a leucine zipper domain and a glutamine-rich C-terminus. Also it is highly expressed in murine testis and is located in the cell nucleus and cytoplasm. The interaction of BS-63 with aF10 (696-1001aa) was validated by surface plasmon resonance and by affinity precipitation combined with Western blot. aF10 (696-1001aa) interacted in vitro with BS-63 extracted from rat testis germ cells. It is hypothesized that BS-63 is a testis-specific nucleoporin and possibly acts as a docking site and a cotransporter of Ran and transportin. The complex performs the task of a carrier system in transporting aF10 into the nucleus of germ cells during spermiogenesis.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • DNA, Complementary / genetics
  • Glycoproteins / chemistry
  • Glycoproteins / genetics*
  • Glycoproteins / isolation & purification
  • Glycoproteins / metabolism*
  • Humans
  • Karyopherins / chemistry
  • Male
  • Mice
  • Microscopy, Electron, Scanning
  • Molecular Sequence Data
  • Nuclear Envelope / chemistry
  • Nuclear Envelope / metabolism
  • Nuclear Pore / chemistry
  • Nuclear Pore / metabolism
  • Nuclear Pore Complex Proteins
  • Nuclear Proteins
  • Organ Specificity
  • Phosphorylation
  • Protein Binding
  • Protein Kinase C / metabolism
  • Protein Transport
  • Sequence Homology, Nucleic Acid
  • Spermatozoa / cytology
  • Spermatozoa / metabolism
  • Spermatozoa / ultrastructure
  • Testis / cytology
  • Testis / metabolism*
  • Transcription Factors / metabolism
  • Two-Hybrid System Techniques
  • ran GTP-Binding Protein / chemistry

Substances

  • DNA, Complementary
  • Glycoproteins
  • Karyopherins
  • MLLT10 protein, human
  • Mllt10 protein, mouse
  • Nuclear Pore Complex Proteins
  • Nuclear Proteins
  • RGPD8 protein, human
  • Transcription Factors
  • Protein Kinase C
  • ran GTP-Binding Protein