Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Pivot Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Target Concepts:
Gene/Protein
Disease
Symptom
Drug
Enzyme
Compound
Query: UNIPROT:P01178 (
oxytocin
)
15,767
document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)
Intranuclear inclusions composed of tubular filaments constitute a pathological hallmark of
oculopharyngeal muscular dystrophy
(
OPMD
). Autosomal dominant
OPMD
is caused by (GCG) repeat expansions in the gene that encodes for poly(A) binding protein nuclear 1 (
PABPN1
). The mutation results in the expansion of a polyalanine stretch in the N-terminus of the protein. It has been proposed that mutated
PABPN1
induces protein aggregation, which in turn causes the formation of the filamentous nuclear inclusions. Here we report the presence of intranuclear inclusions composed of tubular filaments in
oxytocin
-producing neurons from normal rat hypothalamus. Like
OPMD
inclusions, the filamentous structures in neurosecretory neurons accumulate
PABPN1
, poly(A) RNA, ubiquitin and proteasomes. These inclusions do not contain members of Hsp40 and HDJ-2/DNAJ families of chaperones. The proportion of
oxytocin
-producing neurons that contain inclusions decreases during parturition and lactation (when synthesis and release of
oxytocin
is maximal) and increases at 1 day post-weaning (when occurs a drastic reduction in the production of the hormone). Thus,
PABPN1
filaments in normal neurons are dynamic structures, the appearance of which correlate with changes in cellular activity. These data provide the first physiological evidence that polyalanine expansions are not essential to induce polymerization of
PABPN1
into filamentous nuclear inclusions.
...
PMID:Oculopharyngeal muscular dystrophy-like nuclear inclusions are present in normal magnocellular neurosecretory neurons of the hypothalamus. 1497 64
Nuclear aggregation of the expanded polyalanine tract in the poly(A)-binding protein nuclear 1 (
PABPN1
) is the pathological hallmark of
oculopharyngeal muscular dystrophy
. However, wild type
PABPN1
aggregates into nuclear inclusion in
oxytocin
-producing neurons under physiological conditions. In this study we have analyzed the nuclear organization and dynamics of
PABPN1
inclusions in
oxytocin
-producing neurons. We demonstrated that
PABPN1
inclusions represent a distinct compartment of the interchromatin region. They establish a spatial relationship with nuclear speckles, Cajal bodies and clastosomes.
PABPN1
inclusions accumulate poly(A) RNA, but do not concentrate highly expressed mRNAs in
oxytocin
producing neurons and the mRNA-binding proteins hnRNP C, Y14 and REF.
PABPN1
inclusions are dynamic structures that appear during the postnatal period and their number decrease in response to the activation of transcription. Our results support that the RNA retained in the
PABPN1
inclusions is a noncoding regulatory RNA involved in some aspects of nuclear RNA metabolism.
...
PMID:Nuclear compartmentalization and dynamics of the poly(A)-binding protein nuclear 1 (PABPN1) inclusions in supraoptic neurons under physiological and osmotic stress conditions. 1825 12