Genetic analysis of Mint/X11 proteins: essential presynaptic functions of a neuronal adaptor protein family

J Neurosci. 2006 Dec 13;26(50):13089-101. doi: 10.1523/JNEUROSCI.2855-06.2006.

Abstract

Mints/X11s are adaptor proteins composed of three isoforms: neuron-specific Mints 1 and 2, and the ubiquitously expressed Mint 3. We have now analyzed constitutive and conditional knock-out mice for all three Mints/X11s. We found that approximately 80% of mice lacking both neuron-specific Mint isoforms (Mints 1 and 2) die at birth, whereas mice lacking any other combination of Mint isoforms survive normally. The approximately 20% surviving Mint 1/2 double knock-out mice exhibit a decrease in weight and deficits in motor behaviors. Hippocampal slice electrophysiology uncovered a decline in spontaneous neurotransmitter release, lowered synaptic strength, and enhanced paired-pulse facilitation in Mint-deficient mice, suggesting a decreased presynaptic release probability. Acute ablation of Mint expression in cultured neurons from conditional Mint 1/2/3 triple knock-in mice also revealed a decline in spontaneous release, confirming that deletion of Mints impair presynaptic function. Quantitation of synaptic proteins showed that acute deletion of Mints caused a selective increase in Munc18-1 and Fe65 proteins, and overexpression of Munc18-1 in wild-type neurons also produced a decrease in spontaneous release, suggesting that the interaction of Mints with Munc18-1 may contribute to the presynaptic phenotype observed in Mint-deficient mice. Our studies thus indicate that Mints are important regulators of presynaptic neurotransmitter release that are essential for mouse survival.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Adaptor Proteins, Signal Transducing / biosynthesis
  • Adaptor Proteins, Signal Transducing / genetics*
  • Adaptor Proteins, Signal Transducing / physiology
  • Adaptor Proteins, Vesicular Transport / biosynthesis
  • Adaptor Proteins, Vesicular Transport / genetics*
  • Adaptor Proteins, Vesicular Transport / physiology
  • Animals
  • Cells, Cultured
  • DNA-Binding Proteins
  • Hippocampus / physiology
  • Mice
  • Mice, Knockout
  • Mice, Mutant Strains
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics*
  • Nerve Tissue Proteins / physiology
  • Neurons / metabolism
  • Neurons / physiology*
  • Neurotransmitter Agents / metabolism
  • Nuclear Proteins / biosynthesis
  • Nuclear Proteins / genetics*
  • Nuclear Proteins / physiology
  • Presynaptic Terminals / metabolism
  • Presynaptic Terminals / physiology*
  • Protein Isoforms / biosynthesis
  • Protein Isoforms / genetics
  • Proteins / genetics
  • Proteins / metabolism
  • RNA-Binding Proteins
  • Synaptic Transmission / genetics

Substances

  • Adaptor Proteins, Signal Transducing
  • Adaptor Proteins, Vesicular Transport
  • Apba1 protein, mouse
  • Apba3 protein, mouse
  • DNA-Binding Proteins
  • Nerve Tissue Proteins
  • Neurotransmitter Agents
  • Nuclear Proteins
  • Protein Isoforms
  • Proteins
  • RNA-Binding Proteins
  • Spen protein, mouse