The necdin interactome: evaluating the effects of amino acid substitutions and cell stress using proximity-dependent biotinylation (BioID) and mass spectrometry.
We focused on three important regulatory DNA elements which are all differentially methylated regions (DMRs) methylated on the maternal allele: the PWS imprinting center (PWS-IC) which is a germline DMR and the somatic NDN and MKRN3 DMRs hierarchically controlled by PWS-IC.
the single-nucleotide polymorphism rs850807 which is putatively functional and linked with MAGEL2 and NDN Genetic variation in rs850807 was strongly and exclusively associated with the ideas of reference subscale of the schizophrenia spectrum which is best typified as paranoia
One candidate variant was located in an alpha helix of Necdin (NDN) phased to the paternally inherited allele. NDN is maternally imprinted within the 15q11.2 Prader-Willi Syndrome (PWS) region
NDN is an imprinted tumor suppressor gene which affects cancer cell motility invasion and growth and that its loss of function in ovarian cancer can be caused by both genetic and epigenetic mechanisms.
Necdin expression declined during replicative aging of IMR90 primary human fibroblasts or after induction of premature senescence.Showed that in normal human cells Necdin expression mimicked the effect of p53 inactivation by increasing radioresistance.
necdin has multiple roles within protein complexes in different subcellular compartments and indicate that it can utilize multiple karyopherin-dependent pathways to modulate its localization.
Necdin a negative growth regulator identified as a novel STAT3 target gene whose expression is down-regulated at the mRNA and protein levels when STAT3 is constitutively active.
rare variant of necdin (p.V318A) was described in a family with Kallmann syndrome Familial segregation and in vitro analysis suggested that this non-synonymous variant did not have a direct causative role in hypogonadism phenotype.
Data suggest that the effects of necdin deletion on the developing nervous system may depend on the relative expression of p75NTR and TrkA in the cells of particular regions of the nervous system.
Data suggest that Nogo-A is a novel necdin binding protein and inhibits necdin-accelerated neuronal neurite outgrowth by sequestering necdin in the cytoplasm.
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