Literature DB >> 19103300

Characterization of dehydrodolichyl diphosphate synthase gene in rainbow trout (Oncorhynchus mykiss).

Alexander Rebl1, Eckhard Anders, Klaus Wimmers, Tom Goldammer.   

Abstract

Dehydrodolichyl diphosphate synthase (DHDDS) catalyzes cis-prenyl chain elongation to produce the polyprenyl backbone of Dolichol, a glycosyl carrier-lipid required for the co-translational modification of various proteins. The resulting glycoproteins play a role in several physiological and pathological processes. This manuscript characterizes the DHDDS-like gene from rainbow trout (Oncorhynchus mykiss) and its tissue-specific mRNA abundance in two different strains. The ubiquitous expression of DHDDS in trout indicates the essential function of the product Dolichol for metabolic processes. The comparison of the deduced amino acid sequence with DHDDS proteins from different vertebrate, invertebrate, and herbal species reveals a high degree of conserved amino acids and protein regions suggesting a common functional relevance. This is the first report of a prenyltransferase homologue from a teleostean species.

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Year:  2008        PMID: 19103300     DOI: 10.1016/j.cbpb.2008.12.003

Source DB:  PubMed          Journal:  Comp Biochem Physiol B Biochem Mol Biol        ISSN: 1096-4959            Impact factor:   2.231


  4 in total

1.  A missense mutation in DHDDS, encoding dehydrodolichyl diphosphate synthase, is associated with autosomal-recessive retinitis pigmentosa in Ashkenazi Jews.

Authors:  Lina Zelinger; Eyal Banin; Alexey Obolensky; Liliana Mizrahi-Meissonnier; Avigail Beryozkin; Dikla Bandah-Rozenfeld; Shahar Frenkel; Tamar Ben-Yosef; Saul Merin; Sharon B Schwartz; Artur V Cideciyan; Samuel G Jacobson; Dror Sharon
Journal:  Am J Hum Genet       Date:  2011-02-03       Impact factor: 11.025

2.  High Rate of Recurrent De Novo Mutations in Developmental and Epileptic Encephalopathies.

Authors:  Fadi F Hamdan; Candace T Myers; Patrick Cossette; Philippe Lemay; Dan Spiegelman; Alexandre Dionne Laporte; Christina Nassif; Ousmane Diallo; Jean Monlong; Maxime Cadieux-Dion; Sylvia Dobrzeniecka; Caroline Meloche; Kyle Retterer; Megan T Cho; Jill A Rosenfeld; Weimin Bi; Christine Massicotte; Marguerite Miguet; Ledia Brunga; Brigid M Regan; Kelly Mo; Cory Tam; Amy Schneider; Georgie Hollingsworth; David R FitzPatrick; Alan Donaldson; Natalie Canham; Edward Blair; Bronwyn Kerr; Andrew E Fry; Rhys H Thomas; Joss Shelagh; Jane A Hurst; Helen Brittain; Moira Blyth; Robert Roger Lebel; Erica H Gerkes; Laura Davis-Keppen; Quinn Stein; Wendy K Chung; Sara J Dorison; Paul J Benke; Emily Fassi; Nicole Corsten-Janssen; Erik-Jan Kamsteeg; Frederic T Mau-Them; Ange-Line Bruel; Alain Verloes; Katrin Õunap; Monica H Wojcik; Dara V F Albert; Sunita Venkateswaran; Tyson Ware; Dean Jones; Yu-Chi Liu; Shekeeb S Mohammad; Peyman Bizargity; Carlos A Bacino; Vincenzo Leuzzi; Simone Martinelli; Bruno Dallapiccola; Marco Tartaglia; Lubov Blumkin; Klaas J Wierenga; Gabriela Purcarin; James J O'Byrne; Sylvia Stockler; Anna Lehman; Boris Keren; Marie-Christine Nougues; Cyril Mignot; Stéphane Auvin; Caroline Nava; Susan M Hiatt; Martina Bebin; Yunru Shao; Fernando Scaglia; Seema R Lalani; Richard E Frye; Imad T Jarjour; Stéphanie Jacques; Renee-Myriam Boucher; Emilie Riou; Myriam Srour; Lionel Carmant; Anne Lortie; Philippe Major; Paola Diadori; François Dubeau; Guy D'Anjou; Guillaume Bourque; Samuel F Berkovic; Lynette G Sadleir; Philippe M Campeau; Zoha Kibar; Ronald G Lafrenière; Simon L Girard; Saadet Mercimek-Mahmutoglu; Cyrus Boelman; Guy A Rouleau; Ingrid E Scheffer; Heather C Mefford; Danielle M Andrade; Elsa Rossignol; Berge A Minassian; Jacques L Michaud
Journal:  Am J Hum Genet       Date:  2017-11-02       Impact factor: 11.025

3.  Two specific mutations are prevalent causes of recessive retinitis pigmentosa in North American patients of Jewish ancestry.

Authors:  Giulia Venturini; Hanna Koskiniemi-Kuendig; Shyana Harper; Eliot L Berson; Carlo Rivolta
Journal:  Genet Med       Date:  2014-09-25       Impact factor: 8.822

4.  Characterization of Sialic Acid-Binding Immunoglobulin-Type Lectins in Fish Reveals Teleost-Specific Structures and Expression Patterns.

Authors:  Kim F Bornhöfft; Joan Martorell Ribera; Torsten Viergutz; Marzia T Venuto; Ulrike Gimsa; Sebastian P Galuska; Alexander Rebl
Journal:  Cells       Date:  2020-03-31       Impact factor: 6.600

  4 in total

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