Literature DB >> 16469493

Tissue-cell- and species-specific expression of gonadotropin-regulated long chain acyl-CoA synthetase (GR-LACS) in gonads, adrenal and brain. Identification of novel forms in the brain.

Jie Li1, Yi Sheng, Pei Zong Tang, Chon-Hwa Tsai-Morris, Maria L Dufau.   

Abstract

Gonadotropin-regulated long chain acyl-CoA synthetase (GR-LACS) is a novel hormonally regulated fatty acyl-CoA synthetase (FACS) with activity for long-chain fatty acids. The presence of this enzyme in the Leydig cells of the mature rat testis and its mode of regulation suggest that it participates in testicular steroidogenesis. This study demonstrates that GR-LACS expression is tissue, cell and species-specific. The 79 kDa GR-LACS protein is expressed in rodent gonads and brain, and only in the mouse in the adrenal cortex. In the ovary of both species it is associated with follicles undergoing atresia. It is present in the newborn and immature testis tubules and after puberty only in the Leydig cells. A distinct GR-LACS protein species of 64 kDa that was more abundant than the 79 kDa long form was found in the rat brain. Also, a minor 73 kDa form was observed in the rat brain and mouse ovary. Two novel species resulting from alternatively splicing of the GR-LACS gene were identified in a rat brain cDNA library: a short form 1 (S1) lacking exon 8 and short form 2 (S2) lacking exons 6-8. Expression studies revealed that the sizes of the S1/S2 proteins are comparable to those of the endogenous variant species. Neither S form contains FACSs activity, suggesting that exon 8 is essential for the enzymatic function. GR-LACS variants exhibit small but significant dominant negative effects on the FACS activity of the long form. GR-LACS variants may regulate the long form's activity in the brain.

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Year:  2006        PMID: 16469493     DOI: 10.1016/j.jsbmb.2005.10.005

Source DB:  PubMed          Journal:  J Steroid Biochem Mol Biol        ISSN: 0960-0760            Impact factor:   4.292


  6 in total

1.  Characterization of splice variants of the genes encoding human mitochondrial HMG-CoA lyase and HMG-CoA synthase, the main enzymes of the ketogenesis pathway.

Authors:  Beatriz Puisac; Mónica Ramos; María Arnedo; Sebastián Menao; María Concepción Gil-Rodríguez; María Esperanza Teresa-Rodrigo; Angeles Pié; Juan Carlos de Karam; Jan-Jaap Wesselink; Ignacio Giménez; Feliciano J Ramos; Nuria Casals; Paulino Gómez-Puertas; Fausto G Hegardt; Juan Pié
Journal:  Mol Biol Rep       Date:  2011-09-28       Impact factor: 2.316

2.  Multiple erythroid isoforms of human long-chain acyl-CoA synthetases are produced by switch of the fatty acid gate domains.

Authors:  Eric Soupene; Frans A Kuypers
Journal:  BMC Mol Biol       Date:  2006-07-11       Impact factor: 2.946

Review 3.  Function of alternative splicing.

Authors:  Olga Kelemen; Paolo Convertini; Zhaiyi Zhang; Yuan Wen; Manli Shen; Marina Falaleeva; Stefan Stamm
Journal:  Gene       Date:  2012-08-15       Impact factor: 3.688

4.  Chiral separation of ibuprofen and chiral pharmacokinetics in healthy Chinese volunteers.

Authors:  Chaonan Zheng; Haiping Hao; Guangji Wang; Guowei Sang; Jianguo Sun; Peng Li; Jing Li
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2008 Jan-Mar       Impact factor: 2.441

Review 5.  Mammalian long-chain acyl-CoA synthetases.

Authors:  Eric Soupene; Frans A Kuypers
Journal:  Exp Biol Med (Maywood)       Date:  2008-03-28

6.  Characterization of a novel HMG-CoA lyase enzyme with a dual location in endoplasmic reticulum and cytosol.

Authors:  María Arnedo; Sebastián Menao; Beatriz Puisac; María E Teresa-Rodrigo; María C Gil-Rodríguez; Eduardo López-Viñas; Paulino Gómez-Puertas; Nuria Casals; César H Casale; Fausto G Hegardt; Juan Pié
Journal:  J Lipid Res       Date:  2012-07-30       Impact factor: 5.922

  6 in total

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