#Ran-GTP

Protein Sorting and Trafficking

Which of the following processes is not directly dependent on Ran-GTP?

Most nuclear import of NLS proteins using importin-alpha-beta heterodimer and export of NES proteins via CRM1 strictly consume Ran-GTP cycles, with RCC1 generating Ran-GTP inside nucleus and RanGAP1 hydrolyzing outside. Each cycle consumes one GTP and relies on NTF2 recycling of Ran-GDP. Messenger RNA departure follows divergent energetic logic. Bulk poly(A) mRNA transcribed, spliced and polyadenylated recruits TREX complex and adaptor Aly/REF that loads heterodimer NXF1-NXT1 which binds FG repeats directly without Ran. At cytoplasmic filaments of pore, DEAD-box helicase Dbp5/DDX19 activated b

Ref: Stewart M, Nature Rev Mol Cell Biol 8: 2007, Ran-Dependent Protein Transport versus Ran-Independent mRNA Export.

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Protein Sorting and Trafficking

Which protein is responsible for releasing cargo from the importin receptor in the nucleus?

Efficient nuclear import demands timely liberation of cargo after arrival inside nucleoplasm so it can engage chromatin, transcription machinery or splicing. Importin-beta-cargo interaction stable in cytoplasm where Ran-GTP scarce becomes unstable upon encountering high nuclear Ran-GTP concentration. Ran-GTP docks onto N-terminal arch of importin-beta composed of HEAT repeats, inducing large allosteric opening that widens superhelical curvature and disrupts binding interface for importin-alpha IBB domain and for FG nucleoporins. Importin-alpha affinity for basic NLS drops, cargo released aided

Ref: Vetter et al., Nature 392: 1998, RanGTP Dissociates Import Complexes in Nucleus.

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Protein Sorting and Trafficking

What ensures directionality in nuclear protein transport?

Unidirectional accumulation of proteins against concentration gradients through nuclear pores cannot arise from gate selectivity alone because FG nucleoporin mesh permits diffusion in both directions. Direction emerges from asymmetric distribution of Ran regulators generating chemical potential. Nuclear RCC1 bound to chromatin continuously exchanges GDP for GTP using nuclear GTP pool, while cytoplasmic RanGAP1 SUMOylated and tethered to RanBP2/Nup358 plus soluble RanBP1 hydrolyzes GTP outside, creating gradient high inside low outside, more than hundred-fold difference. Importins bind NLS carg

Ref: Nature Reviews Mol Cell Biol 20: 2019, Ran GTPase Gradient as Directionality Determinant in Nuclear Transport.

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Protein Sorting and Trafficking

Ran-GTP is primarily involved in:

Directionality of nucleocytoplasmic transport relies on asymmetric distribution of small GTPase Ran nucleotide states forming gradient across nuclear envelope. Regulator RCC1 RanGEF bound to chromatin generates high Ran-GTP concentration inside nucleus through exchange of GDP for GTP, while cytoplasmic filaments of nuclear pore complex associated with RanGAP and RanBP1 stimulate GTP hydrolysis to Ran-GDP in cytosol, depleting Ran-GTP outside. Importin alpha/beta-cargo complexes formed in cytoplasm traverse pore via interactions with FG nucleoporins, encountering Ran-GTP in nucleus which binds

Ref: Gorlich & Kutay, Annu Rev Cell Dev Biol 1999, Ran Gradient. Alberts 7th ed., Chapter 12, Transport.

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