Cited by 113Neuroscience and Neuropharmacology ResearchReceptor Mechanisms and SignalingNicotinic Acetylcholine Receptors Study

Cloning, Expression Patterns, and Chromosome Localization of Three Human and Two Mouse Homologues of GABAA Receptor-Associated Protein

Xin, Yurong, Yu, Long, Chen, Zheng, Zheng, Lihua, Fu, Qiang, Jiang, Jianmin, Zhang, Pingzhao, Gong, Romu +1 more·2001·Genomics

Abstract

Type A receptors of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter, contain alpha, beta, delta, gamma, and rho subunits. The gamma subunit has four subtypes: gamma1, gamma2, gamma3, andgamma4. GABA(A) receptor-associated protein (GABARAP) was previously demonstrated to act as a linker protein between microtubules and the gamma2 subunit of GABA(A) receptors. However, no other linker proteins have been identified as mediating the linkage of microtubules and the remaining subunits of GABA(A) receptors. In this study we identified three human paralogues (GABARAPL1, GABARAPL2, and GABARAPL3) and two mouse orthologues (Gabarapl1 and Gabarapl2) of human GABARAP, all of which encoded 117 amino acids, as does Gabarapl. The expression patterns of GABARAPL1, GABARAPL2, and GABARAP in 16 adult tissues showed that they were expressed ubiquitously. The expression levels of GABARAPL1 as a 2.3-kb transcript were very high in brain, heart, peripheral blood leukocytes, liver, kidney, placenta, and skeletal muscle, very low in thymus and small intestine, and moderate in other tissues tested. The unique 1.35-kb transcript of GABARAPL2 was expressed at high levels in heart, brain, testis, prostate, ovary, spleen, and skeletal muscle, at very low levels in lung, thymus, and small intestine, and moderately in other tissues tested. For GABARAP, a 1.3-kb transcript was abundantly expressed in all tested tissues with small variation. The expression patterns of Gabarapl1 and Gabarapl2 w…

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Crossref · 10.1006/geno.2001.6555

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  • The second GABARAP/GATE subfamily comprises GABARAP, GABARAPL1, GATE-16 (aka GABARAPL2) and GABARAP-L3.

    “The second, the GABARAP/GATE subfamily, comprises GABARAP, GABARAPL1, GATE-16 (aka GABARAPL2) and GABARAP-L3 [29,30].”

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Authors
Xin, Y., Yu, L., Chen, Z., Zheng, L., Fu, Q., Jiang, J., Zhang, P., Gong, R., & Zhao, S.
Affiliations
Fudan University (CN)
Corresponding author
Yu, Long
Venue
Genomics
Publisher
Elsevier BV
Published
2001-06
Volume
74
Issue
3
Pages
408-413
ISSN
0888-7543 (ISSN-L)
OpenAlex
W1966635422
Cited by
113
References
0
Citations by year
2026: 2 · 2024: 3 · 2023: 5 · 2022: 3 · 2021: 8 · 2020: 4 · 2019: 2 · 2018: 2 · 2017: 2 · 2016: 6 · 2015: 6 · 2014: 4 · 2013: 5 · 2012: 9
FWCI
1.85
Type
journal article
Language
en
Open access
closed
Locations
  • Genomics (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Receptor Mechanisms and Signaling
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nicotinic Acetylcholine Receptors Study
Keywords
GABARAP, GABARAPL1, GABARAPL2, GABAA receptor, gamma subunit, gene cloning, tissue expression pattern, chromosomal localization, human-mouse sequence comparison
MeSH terms
Amino Acid Sequence, Animals, Base Sequence, Chromosome Mapping, Chromosomes, Human, Pair 12, Chromosomes, Human, Pair 15, Chromosomes, Human, Pair 16, Cloning, Molecular, Female, Humans, Male, Microtubule-Associated Proteins, Molecular Sequence Data, RNA, Tissue Distribution, Blotting, Northern, Gene Expression, Sequence Alignment, Sequence Homology, Amino Acid, Sequence Analysis, DNA, DNA, Complementary, Protein Isoforms, Radiation Hybrid Mapping, Adaptor Proteins, Signal Transducing, Apoptosis Regulatory Proteins, Mice

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