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January 15, 1993Science337 citations

Retinal Degeneration in Choroideremia: Deficiency of Rab Geranylgeranyl Transferase

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MSMiguel C. SeabraMBMichael S. BrownJGJoseph L. Goldstein

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Abstract

Rab geranylgeranyl transferase (GG transferase) is a two-component enzyme that attaches 20-carbon isoprenoid groups to cysteine residues in Rab proteins, a family of guanosine triphosphate-binding proteins that regulate vesicular traffic. The mutant gene in human choroideremia, an X-linked form of retinal degeneration, encodes a protein that resembles component A of rat Rab GG transferase. Lymphoblasts from choroideremia subjects showed a marked deficiency in the activity of component A, but not component B, of Rab GG transferase. The deficiency was more pronounced when the substrate was Rab3A, a synaptic vesicle protein, than it was when the substrate was Rab1A, a protein of the endoplasmic reticulum. The data imply the existence of multiple component A proteins, one of which is missing in choroideremia.

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Cite This Study

Seabra et al. (1993) studied this question.

synapsesocial.com/papers/69d73d76aa68b335b4f30a23https://doi.org/10.1126/science.8380507
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Purification of component A of Rab geranylgeranyl transferase: Possible identity with the choroideremia gene product1992 · 302 citations
  2. 2An autosomal homologue of the choroideremia gene colocalizes with the usher syndrome type II locus on the distal part of chromosome 1q1992 · 73 citations
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  4. 4Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa1991 · 473 citations
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