[Fragile X mental retardation protein interacts with human NDK/Nm23-H2]

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2001 Dec;23(6):580-4.
[Article in Chinese]

Abstract

Objective: To investigate the physiological role of fragile X mental retardation protein (FMRP) and screen the proteins interacting with FMRP in human fetal hippocampus cDNA library.

Methods: Human fetal hippocampus cDNA library was constructed in yeast two-hybrid DAD vector pGAD10. Quality of the library was measured by picking up random colonies as templates for PCR testing. Proteins interacting with FMRP were screened by yeast two-hybrid system. Furthermore, the interaction site of FMRP was mapped in yeast.

Results: The average length of inserts of the two-hybrid library was 1.5 kb, and the ratio of recombinant colonies was about 90%. Human NDK/Nm23-H2 was found interacting with FMRP. NDK/Nm23-H2 interacted with FMRP exon 1-12, as well as FMRP isoforms without exon 12, and exons 14-17. NDK/Nm23-H2 couldn't interact with FMRP exon 1-6 and exon 2-7 fragments.

Conclusions: Human NDK/Nm23-H2 can bind FMRP directly. The interaction site of FMRP is located at its exon 1-11. This interaction in vitro might alter the intracellular distribution of NDK/Nm23-H2, and even regulates the transcription and expression of FMRP.

Publication types

  • English Abstract
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Fragile X Mental Retardation Protein
  • Fragile X Syndrome* / metabolism
  • Humans
  • In Vitro Techniques
  • NM23 Nucleoside Diphosphate Kinases
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism*
  • Nucleoside-Diphosphate Kinase / metabolism*
  • Protein Binding
  • Proteins / metabolism*
  • RNA-Binding Proteins / genetics
  • RNA-Binding Proteins / metabolism*
  • Recombinant Proteins / metabolism
  • Two-Hybrid System Techniques

Substances

  • FMR1 protein, human
  • NM23 Nucleoside Diphosphate Kinases
  • Nerve Tissue Proteins
  • Proteins
  • RNA-Binding Proteins
  • Recombinant Proteins
  • Fragile X Mental Retardation Protein
  • NME1 protein, human
  • Nucleoside-Diphosphate Kinase