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Nucleocytoplasmic Transport: Integrating mRNA Production and Turnover with Export through the Nuclear Pore

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Separation of the nucleus and cytoplasm, maintained by two membrane bilayers that form the nuclear envelope, allows for spatial control over transcription factors and signaling molecules. This compartmentalization further ensures the presence of specialized environments for different stages of gene expression, such as transcription and protein production. Selective exchange between these two compartments is clearly important as well. Whereas many types of active transport between the nucleus and cytoplasm rely on transport receptors in the importin-β superfamily, export of mRNA utilizes distinct soluble machinery (6, 92). Moreover, in general mRNA export does not depend on a specific motif in the cargo, as has been demonstrated in many other cases of receptor-cargo interactions (22). Recent progress in identifying soluble factors important to mRNA trafficking is beginning to reveal the molecular basis for functional coupling between steps in mRNA biogenesis and how such coupling, rather than a consensus motif, brings specificity to mRNA export.

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