Abstract
Nucleocytoplasmic transport of rat liver mRNA is thought to be regulated by a nucleoside triphosphatase whose activity in the intact nuclear envelope is stimulated by the 3'poly(A) tail of poly(A)+ mRNA. In contrast to the liver mRNA, the mRNA from rat brain contains a great population of poly(A)- mRNA's that does not appear until after birth. Measurements of the nuclear-envelope-associated enzyme activities involved in mRNA transport, and their dependence on endogenous (isolated cytoplasmic mRNA-transport-stimulating proteins) and exogenous (poly(A), lectins, and neoglycoproteins) factors during prenatal and postnatal rat brain and liver development, revealed marked organ-dependent differences paralleling the appearance of the poly(A)- mRNA unique in the brain.
Publication types
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Comparative Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Biological Transport
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Brain / growth & development
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Brain / metabolism*
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Carrier Proteins / metabolism
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Cell Nucleus / metabolism
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Cytoplasm / metabolism
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Enzyme Activation / drug effects
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Glycoproteins / pharmacology
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Lectins / pharmacology
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Liver / growth & development
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Liver / metabolism*
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Nuclear Envelope / enzymology
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Nucleocytoplasmic Transport Proteins*
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Nucleoside-Triphosphatase
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Phosphoric Monoester Hydrolases / metabolism
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Poly A / metabolism*
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Poly A / pharmacology
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RNA, Messenger / metabolism*
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RNA-Binding Proteins*
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Rats
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Rats, Inbred Strains
Substances
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Carrier Proteins
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Glycoproteins
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Lectins
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Nucleocytoplasmic Transport Proteins
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RNA, Messenger
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RNA-Binding Proteins
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Poly A
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Phosphoric Monoester Hydrolases
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Nucleoside-Triphosphatase