Literature DB >> 12811562

The human sugar-phosphate/phosphate exchanger family SLC37.

Lucia Bartoloni1, Stylianos E Antonarakis.   

Abstract

The SLC37 family of four predicted proteins is an almost unexplored group of transmembrane sugar transporters. Of the four proteins/genes assigned to date to this family, only one is well known, the SLC37A4 gene (also known as the glucose-6-phosphate transporter 1, G6PT1) mutated in the glycogen storage disease non-1A type. Data on SLC3A1 gene expression are available for humans, while data on SLC37A2 are available for mice. The last SLC37 family member, SLC37A3, is only a putative gene/protein identified by in silico analyses. The four genes are not clustered in a single chromosome as regions and the identity of their predicted polypeptides is between 60 and 20%. Here we propose a new nomenclature for the SLC37 proteins (SPX: sugar- phosphate e xchangers) numbered according to the gene numbering.

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Year:  2003        PMID: 12811562     DOI: 10.1007/s00424-003-1105-0

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  12 in total

1.  Type-1c glycogen storage disease is not caused by mutations in the glucose-6-phosphate transporter gene.

Authors:  B Lin; H Hiraiwa; C J Pan; R C Nordlie; J Y Chou
Journal:  Hum Genet       Date:  1999-11       Impact factor: 4.132

Review 2.  The molecular basis of the hepatic microsomal glucose-6-phosphatase system.

Authors:  A Burchell; I D Waddell
Journal:  Biochim Biophys Acta       Date:  1991-04-17

3.  Identification of the glpT-encoded sn-glycerol-3-phosphate permease of Escherichia coli, an oligomeric integral membrane protein.

Authors:  T J Larson; G Schumacher; W Boos
Journal:  J Bacteriol       Date:  1982-12       Impact factor: 3.490

4.  Cloning and characterization of a putative human glycerol 3-phosphate permease gene (SLC37A1 or G3PP) on 21q22.3: mutation analysis in two candidate phenotypes, DFNB10 and a glycerol kinase deficiency.

Authors:  L Bartoloni; M Wattenhofer; J Kudoh; A Berry; K Shibuya; K Kawasaki; J Wang; S Asakawa; I Talior; B Bonne-Tamir; C Rossier; J Michaud; E R McCabe; S Minoshima; N Shimizu; H S Scott; S E Antonarakis
Journal:  Genomics       Date:  2000-12-01       Impact factor: 5.736

5.  Molecular Genetics of Type 1 Glycogen Storage Diseases.

Authors: 
Journal:  Trends Endocrinol Metab       Date:  1999-04       Impact factor: 12.015

6.  Identification of cAMP analogue inducible genes in RAW264 macrophages.

Authors:  Y Takahashi; M Miyata; P Zheng; T Imazato; A Horwitz; J D Smith
Journal:  Biochim Biophys Acta       Date:  2000-07-24

7.  Sequence of a putative glucose 6-phosphate translocase, mutated in glycogen storage disease type Ib.

Authors:  I Gerin; M Veiga-da-Cunha; Y Achouri; J F Collet; E Van Schaftingen
Journal:  FEBS Lett       Date:  1997-12-15       Impact factor: 4.124

8.  Quantitative analysis of glucose-6-phosphate translocase gene expression in various human tissues and haematopoietic progenitor cells.

Authors:  K Ihara; A Nomura; S Hikino; H Takada; T Hara
Journal:  J Inherit Metab Dis       Date:  2000-09       Impact factor: 4.982

9.  Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b.

Authors:  H Hiraiwa; C J Pan; B Lin; S W Moses; J Y Chou
Journal:  J Biol Chem       Date:  1999-02-26       Impact factor: 5.157

10.  Genomic structure of the human glucose 6-phosphate translocase gene and novel mutations in the gene of a Japanese patient with glycogen storage disease type Ib.

Authors:  K Ihara; R Kuromaru; T Hara
Journal:  Hum Genet       Date:  1998-10       Impact factor: 4.132

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  12 in total

1.  The Concise Guide to PHARMACOLOGY 2013/14: transporters.

Authors:  Stephen P H Alexander; Helen E Benson; Elena Faccenda; Adam J Pawson; Joanna L Sharman; Michael Spedding; John A Peters; Anthony J Harmar
Journal:  Br J Pharmacol       Date:  2013-12       Impact factor: 8.739

Review 2.  The SLC37 family of sugar-phosphate/phosphate exchangers.

Authors:  Janice Y Chou; Brian C Mansfield
Journal:  Curr Top Membr       Date:  2014       Impact factor: 3.049

Review 3.  The SLC37 family of phosphate-linked sugar phosphate antiporters.

Authors:  Janice Y Chou; Hyun Sik Jun; Brian C Mansfield
Journal:  Mol Aspects Med       Date:  2013 Apr-Jun

4.  SLC37A1 and SLC37A2 are phosphate-linked, glucose-6-phosphate antiporters.

Authors:  Chi-Jiunn Pan; Shih-Yin Chen; Hyun Sik Jun; Su Ru Lin; Brian C Mansfield; Janice Y Chou
Journal:  PLoS One       Date:  2011-09-20       Impact factor: 3.240

5.  Upregulated solute carrier family 37 member 1 in colorectal cancer is associated with poor patient outcome and metastasis.

Authors:  Daiki Kikuchi; Motonobu Saito; Katsuharu Saito; Yohei Watanabe; Yoshiko Matsumoto; Yasuyuki Kanke; Hisashi Onozawa; Suguru Hayase; Wataru Sakamoto; Teruhide Ishigame; Tomoyuki Momma; Shinji Ohki; Seiichi Takenoshita
Journal:  Oncol Lett       Date:  2017-12-08       Impact factor: 2.967

6.  Analysis and update of the human solute carrier (SLC) gene superfamily.

Authors:  Lei He; Konstandinos Vasiliou; Daniel W Nebert
Journal:  Hum Genomics       Date:  2009-01       Impact factor: 4.639

7.  Dynamically regulated miRNA-mRNA networks revealed by exercise.

Authors:  Alexander G Tonevitsky; Diana V Maltseva; Asghar Abbasi; Timur R Samatov; Dmitry A Sakharov; Maxim U Shkurnikov; Alexey E Lebedev; Vladimir V Galatenko; Anatoly I Grigoriev; Hinnak Northoff
Journal:  BMC Physiol       Date:  2013-06-07

8.  Gene expression of transporters and phase I/II metabolic enzymes in murine small intestine during fasting.

Authors:  Heleen M van den Bosch; Meike Bünger; Philip J de Groot; Jolanda van der Meijde; Guido J E J Hooiveld; Michael Müller
Journal:  BMC Genomics       Date:  2007-08-07       Impact factor: 3.969

9.  PPARalpha-mediated effects of dietary lipids on intestinal barrier gene expression.

Authors:  Heleen M de Vogel-van den Bosch; Meike Bünger; Philip J de Groot; Hanneke Bosch-Vermeulen; Guido J E J Hooiveld; Michael Müller
Journal:  BMC Genomics       Date:  2008-05-19       Impact factor: 3.969

10.  Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.

Authors:  Maria Carla Proverbio; Eleonora Mangano; Alessandra Gessi; Roberta Bordoni; Roberta Spinelli; Rosanna Asselta; Paola Sogno Valin; Stefania Di Candia; Ilaria Zamproni; Cecilia Diceglie; Stefano Mora; Manuela Caruso-Nicoletti; Alessandro Salvatoni; Gianluca De Bellis; Cristina Battaglia
Journal:  PLoS One       Date:  2013-07-15       Impact factor: 3.240

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