Expression and functional significance of mouse paraspeckle protein 1 on spermatogenesis

Biol Reprod. 2004 Sep;71(3):926-32. doi: 10.1095/biolreprod.104.028159. Epub 2004 May 12.

Abstract

Paraspeckle protein 1 (PSP1) in humans is a recently identified component protein of a novel nuclear body, paraspeckle. The protein has a DBHS (Drosophila behavior, human splicing) motif that is found in PSF and p54(nrb)/NonO proteins. These DBHS-containing proteins have been reported to be involved in various nuclear events such as DNA replication, transcription, and mRNA processing. Here we show that mouse paraspeckle protein 1 (mPSP1; encoded by the Pspc1 gene) has two isoforms with different C-termini lengths. Abundant expression of the longer isoform (mPSP1-alpha) and the shorter one (mPSP1-beta) were observed in testis and kidney, respectively. Transiently expressed mPSP1-alpha was localized in nuclei, but mPSP1-beta was localized in both nuclei and cytoplasm. These observations suggest that alternative splicing regulates tissue distribution and subcellular localization. Like other DBHS-containing proteins, mPSP1 has RNA-binding activity. In mouse testis, mPSP1-alpha was found in the nuclear matrix fraction. Furthermore, by coimmunoprecipitation, we confirmed that mPSP1 interacts with other DBHS-containing proteins, PSF and p54(nrb)/NonO. Therefore, we conclude that mPSP1 may regulate multiple phases of important nuclear events during spermatogenesis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Chromatin / physiology
  • DNA-Binding Proteins
  • Gene Expression Regulation, Developmental
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Molecular Sequence Data
  • NIH 3T3 Cells
  • Nuclear Matrix / metabolism
  • Nuclear Matrix-Associated Proteins / metabolism
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / metabolism
  • Octamer Transcription Factors
  • PTB-Associated Splicing Factor
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • RNA-Binding Proteins / genetics*
  • RNA-Binding Proteins / metabolism
  • Spermatogenesis / physiology*
  • Transcriptional Activation / physiology

Substances

  • Chromatin
  • DNA-Binding Proteins
  • NONO protein, human
  • Nuclear Matrix-Associated Proteins
  • Nuclear Proteins
  • Octamer Transcription Factors
  • PSPC1 protein, human
  • PTB-Associated Splicing Factor
  • RNA, Messenger
  • RNA-Binding Proteins
  • paraspeckle protein 1, mouse

Associated data

  • GENBANK/AK017689