Literature DB >> 8093354

A rat brain cDNA encoding the neurotransmitter transporter with an unusual structure.

Q R Liu1, S Mandiyan, B López-Corcuera, H Nelson, N Nelson.   

Abstract

A rat cDNA clone encoding the novel membrane protein of the neurotransmitter transporters family was cloned and sequenced. The cDNA was identified as a transcript of the gene NTT4 of which a partial genomic clone was previously sequenced. Alignment of the amino acid sequence of NTT4 with other members of the neurotransmitter transporter family revealed a marked deviation from the conserved structure of all other members of the family. The largest extracellular loop with a potential glycosylation site was identified between membrane segments 7 and 8. The protein retains the common glycosylated loop between transmembrane helices 3 and 4 in all members of the family. The transcript of NTT4 was found exclusively in the central nervous system and is more abundant in the cerebellum and the cerebral cortex.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8093354     DOI: 10.1016/0014-5793(93)81145-p

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  14 in total

Review 1.  The solute carrier 6 family of transporters.

Authors:  Stefan Bröer; Ulrik Gether
Journal:  Br J Pharmacol       Date:  2012-09       Impact factor: 8.739

Review 2.  Molecular biology of glycinergic neurotransmission.

Authors:  F Zafra; C Aragón; C Giménez
Journal:  Mol Neurobiol       Date:  1997-06       Impact factor: 5.590

3.  GABA transporters in Drosophila melanogaster: molecular cloning, behavior, and physiology.

Authors:  W S Neckameyer; R L Cooper
Journal:  Invert Neurosci       Date:  1998-03

Review 4.  Transporters for nitrogenous compounds in plants.

Authors:  W B Frommer; M Kwart; B Hirner; W N Fischer; S Hummel; O Ninnemann
Journal:  Plant Mol Biol       Date:  1994-12       Impact factor: 4.076

Review 5.  Sodium ion-dependent transporters for neurotransmitters: a review of recent developments.

Authors:  D M Worrall; D C Williams
Journal:  Biochem J       Date:  1994-02-01       Impact factor: 3.857

6.  Homozygous SLC6A17 mutations cause autosomal-recessive intellectual disability with progressive tremor, speech impairment, and behavioral problems.

Authors:  Zafar Iqbal; Marjolein H Willemsen; Marie-Amélie Papon; Luciana Musante; Marco Benevento; Hao Hu; Hanka Venselaar; Willemijn M Wissink-Lindhout; Anneke T Vulto-van Silfhout; Lisenka E L M Vissers; Arjan P M de Brouwer; Sylviane Marouillat; Thomas F Wienker; Hans Hilger Ropers; Kimia Kahrizi; Nael Nadif Kasri; Hossein Najmabadi; Frédéric Laumonnier; Tjitske Kleefstra; Hans van Bokhoven
Journal:  Am J Hum Genet       Date:  2015-02-19       Impact factor: 11.025

7.  Synaptic Vesicle Protein NTT4/XT1 (SLC6A17) Catalyzes Na+-coupled Neutral Amino Acid Transport.

Authors:  Kimberly A Zaia; Richard J Reimer
Journal:  J Biol Chem       Date:  2009-01-15       Impact factor: 5.157

8.  The glycinergic system in human startle disease: a genetic screening approach.

Authors:  Jeff S Davies; Seo-Kyung Chung; Rhys H Thomas; Angela Robinson; Carrie L Hammond; Jonathan G L Mullins; Eloisa Carta; Brian R Pearce; Kirsten Harvey; Robert J Harvey; Mark I Rees
Journal:  Front Mol Neurosci       Date:  2010-03-23       Impact factor: 5.639

9.  Hypertension and impaired glycine handling in mice lacking the orphan transporter XT2.

Authors:  Hui Quan; Krairerk Athirakul; William C Wetsel; Gonzalo E Torres; Robert Stevens; Y T Chen; Thomas M Coffman; Marc G Caron
Journal:  Mol Cell Biol       Date:  2004-05       Impact factor: 4.272

10.  PC12 variants deficient in norepinephrine transporter mRNA have wild type activities of several other related transporters.

Authors:  K Houben; K Dardashti; B D Howard
Journal:  Neurochem Res       Date:  1994-06       Impact factor: 3.996

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.