Literature DB >> 16125675

The repertoire of solute carriers of family 6: identification of new human and rodent genes.

Pär J Höglund1, Dijana Adzic, Sara J Scicluna, Jonas Lindblom, Robert Fredriksson.   

Abstract

Tremendous amount of primary sequence information has been made available from the genome sequencing projects, although a complete annotation and identification of all genes is still far from being complete. Here, we present the identification of two new human genes from the pharmacologically important family of transporter proteins, solute carriers family 6 (SLC6). These were named SLC6A17 and SLC6A18 by HUGO. The human repertoire of SLC6 proteins now consists of 19 functional members and four pseudogenes. We also identified the corresponding orthologues and additional genes from mouse and rat genomes. Detailed phylogenetic analysis of the entire family of SLC6 proteins in mammals shows that this family can be divided into four subgroups. We used Hidden Markov Models for these subgroups and identified in total 430 unique SLC6 proteins from 10 animal, one plant, two fungi, and 196 bacterial genomes. It is evident that SLC6 proteins are present in both animals and bacteria, and that three of the four subfamilies of mammalian SLC6 proteins are present in Caenorhabditis elegans, showing that these subfamilies are evolutionary very ancient. Moreover, we performed tissue localization studies on the entire family of SLC6 proteins on a panel of 15 rat tissues and further, the expression of three of the new genes was studied using quantitative real-time PCR showing expression in multiple central and peripheral tissues. This paper presents an overall overview of the gene repertoire of the SLC6 gene family and its expression profile in rats.

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Year:  2005        PMID: 16125675     DOI: 10.1016/j.bbrc.2005.08.048

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  23 in total

1.  Isolation and molecular characterization of the porcine SLC6A14 gene excludes it as a candidate gene for fat deposition and growth.

Authors:  G L Yang; J Ren; S H Zhang; W B Huang; Y M Guo; Y Y Duan; M Z Liu; L S Huang
Journal:  J Appl Genet       Date:  2010       Impact factor: 3.240

2.  C6ORF192 forms a unique evolutionary branch among solute carriers (SLC16, SLC17, and SLC18) and is abundantly expressed in several brain regions.

Authors:  Josefin A Jacobsson; Olga Stephansson; Robert Fredriksson
Journal:  J Mol Neurosci       Date:  2009-08-21       Impact factor: 3.444

3.  The origin and evolution of vertebrate glycine transporters.

Authors:  Max Shpak; Luciana Girotto Gentil; Manuel Miranda
Journal:  J Mol Evol       Date:  2014-03-12       Impact factor: 2.395

4.  Genomic study and Medical Subject Headings enrichment analysis of early pregnancy rate and antral follicle numbers in Nelore heifers.

Authors:  G A Oliveira Júnior; B C Perez; J B Cole; M H A Santana; J Silveira; G Mazzoni; R V Ventura; M L Santana Júnior; H N Kadarmideen; D J Garrick; J B S Ferraz
Journal:  J Anim Sci       Date:  2017-11       Impact factor: 3.159

5.  SLC6 family transporter SNF-10 is required for protease-mediated activation of sperm motility in C. elegans.

Authors:  Kristin E Fenker; Angela A Hansen; Conrad A Chong; Molly C Jud; Brittany A Duffy; J Paul Norton; Jody M Hansen; Gillian M Stanfield
Journal:  Dev Biol       Date:  2014-06-12       Impact factor: 3.582

Review 6.  X-linked creatine transporter deficiency: clinical aspects and pathophysiology.

Authors:  Jiddeke M van de Kamp; Grazia M Mancini; Gajja S Salomons
Journal:  J Inherit Metab Dis       Date:  2014-05-01       Impact factor: 4.982

7.  Synergy and specificity of two Na+-aromatic amino acid symporters in the model alimentary canal of mosquito larvae.

Authors:  Bernard A Okech; Ella A Meleshkevitch; Melissa M Miller; Lyudmila B Popova; William R Harvey; Dmitri Y Boudko
Journal:  J Exp Biol       Date:  2008-05       Impact factor: 3.312

8.  Infantile convulsions with paroxysmal dyskinesia (ICCA syndrome) and copy number variation at human chromosome 16p11.

Authors:  Patrice Roll; Damien Sanlaville; Jennifer Cillario; Audrey Labalme; Nadine Bruneau; Annick Massacrier; Marc Délepine; Philippe Dessen; Vladimir Lazar; Andrée Robaglia-Schlupp; Gaëtan Lesca; Elisabeth Jouve; Gabrielle Rudolf; Jacques Rochette; G Mark Lathrop; Pierre Szepetowski
Journal:  PLoS One       Date:  2010-10-29       Impact factor: 3.240

9.  Iminoglycinuria and hyperglycinuria are discrete human phenotypes resulting from complex mutations in proline and glycine transporters.

Authors:  Stefan Bröer; Charles G Bailey; Sonja Kowalczuk; Cynthia Ng; Jessica M Vanslambrouck; Helen Rodgers; Christiane Auray-Blais; Juleen A Cavanaugh; Angelika Bröer; John E J Rasko
Journal:  J Clin Invest       Date:  2008-11-06       Impact factor: 14.808

10.  Lhx2 specifies regional fate in Emx1 lineage of telencephalic progenitors generating cerebral cortex.

Authors:  Shen-Ju Chou; Carlos G Perez-Garcia; Todd T Kroll; Dennis D M O'Leary
Journal:  Nat Neurosci       Date:  2009-10-11       Impact factor: 24.884

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