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EXOSC9 encodes a component of the human exosome, a exoribonuclease complex which processes and degrades RNA in the nucleus and cytoplasm. Additionally we are shipping EXOSC9 Antibodies (47) and EXOSC9 Kits (1) and many more products for this protein.
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inactivation of both exosc9, which encodes a component of the RNA exosome, and ptbp1, which encodes an RNA-binding protein abundant in Xenopus embryonic skin, impairs embryonic Xenopus skin development.
Although not required for exosome stability, PM/Scl-100 (show EXOSC10 Proteins) and PM/Scl-75 are involved in mRNA degradation.
Protein-protein interactions between human exosome components support the assembly of RNase PH-type subunits into a six-membered PNPase (show PNPT1 Proteins)-like ring.
The association of the human PM/Scl-75 autoantigen with the exosome is dependent on a newly identified N terminus.
The mammalian exosome mediates the efficient degradation of mRNAs that contain AU-rich elements, possibly by direct binding of PM/Scl-75 to these RNA regions.
PM-Scl-75 is the main autoantigen in patients with the polymyositis/scleroderma overlap syndrome.
This gene encodes a component of the human exosome, a exoribonuclease complex which processes and degrades RNA in the nucleus and cytoplasm. This component may play a role in mRNA degradation and the polymyositis/scleroderma autoantigen complex. Alternative splicing results in multiple transcript variants.
, exosome complex exonuclease RRP45
, exosome component 9
, exosome complex exonuclease RRP45-like
, polymyositis/scleroderma autoantigen 1
, P75 polymyositis-scleroderma overlap syndrome associated autoantigen
, P75 polymyositis-scleroderma overlap syndrome-associated autoantigen
, PMSCL autoantigen, 75kD
, autoantigen PM/Scl 1
, exosome complex component RRP45
, polymyositis/scleroderma autoantigen 1, 75kDa
, polymyositis/scleroderma autoantigen 75 kDa