Literature DB >> 17924204

Characterization of the human CUTA isoform2 present in the stably transfected HeLa cells.

Jingchun Yang1, Huirong Yang, Lichong Yan, Liu Yang, Long Yu.   

Abstract

CUTA, Homo sapiens divalent cation tolerance homolog, has been implicated in anchoring of acetylcholinesterase in neuronal cell membranes. However, a protein highly homologous to CUTA in Rattus norvegicus is structurally similar to the signal transduction protein PII, and this similarity suggests an intriguing role of CUTA in signal transduction. Recent researches indicated that CUTA was one of the 35 key genes responsible for lactation in mammary gland development. However, the physiological role of CUTA is still unclear, so more information of this gene is needed. In this study, the expression profile of CUTA gene in human tissues was examined, and our research revealed that CUTA gene was constitutively expressed in all of the 18 tissues tested. As reported, CUTA gene has five variant transcripts encoding three isoforms with different N terminals. CUTA isoform2 is encoded by three of the five variant transcripts as the common part of the three isoforms. So CUTA isoform2 was chose as representative to characterize the CUTA protein. We constructed a HeLa cell line stably transfected with the encoding sequence of CUTA isoform2 for further study. The subcellular location and oligomeric structure of the CUTA isoform2 was analyzed in the stable cell lines. It was found that the CUTA isoform2 was mainly located in mitochondria as a new potential mitochondrial protein. Furthermore, CUTA isoform2 formed trimers in cell lysate with the possible occurrence of heteropolymers. These findings would be helpful to the further study on the specific function of CUTA protein.

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Year:  2007        PMID: 17924204     DOI: 10.1007/s11033-007-9152-9

Source DB:  PubMed          Journal:  Mol Biol Rep        ISSN: 0301-4851            Impact factor:   2.316


  14 in total

1.  X-ray crystal structure of CutA from Thermotoga maritima at 1.4 A resolution.

Authors:  Alexei Savchenko; Tatiana Skarina; Elena Evdokimova; James D Watson; Roman Laskowski; Cheryl H Arrowsmith; Aled M Edwards; Andrzej Joachimiak; Rong-guang Zhang
Journal:  Proteins       Date:  2004-01-01

2.  Gametes alter the oviductal secretory proteome.

Authors:  A Stephen Georgiou; Edita Sostaric; Chi H Wong; Ambrosius P L Snijders; Phillip C Wright; Harry D Moore; Alireza Fazeli
Journal:  Mol Cell Proteomics       Date:  2005-08-16       Impact factor: 5.911

3.  Large-scale analysis of the human and mouse transcriptomes.

Authors:  Andrew I Su; Michael P Cooke; Keith A Ching; Yaron Hakak; John R Walker; Tim Wiltshire; Anthony P Orth; Raquel G Vega; Lisa M Sapinoso; Aziz Moqrich; Ardem Patapoutian; Garret M Hampton; Peter G Schultz; John B Hogenesch
Journal:  Proc Natl Acad Sci U S A       Date:  2002-03-19       Impact factor: 11.205

4.  Construction of a high-resolution 2.5-Mb transcript map of the human 6p21.2-6p21.3 region immediately centromeric of the major histocompatibility complex.

Authors:  N Tripodis; S Palmer; S Phillips; S Milne; S Beck; J Ragoussis
Journal:  Genome Res       Date:  2000-04       Impact factor: 9.043

5.  Hydrophobic protein that copurifies with human brain acetylcholinesterase: amino acid sequence, genomic organization, and chromosomal localization.

Authors:  D S Navaratnam; F S Fernando; J D Priddle; K Giles; S M Clegg; D J Pappin; I Craig; A D Smith
Journal:  J Neurochem       Date:  2000-05       Impact factor: 5.372

6.  Two distinct proteins are associated with tetrameric acetylcholinesterase on the cell surface.

Authors:  A L Perrier; X Cousin; N Boschetti; R Haas; J M Chatel; S Bon; W L Roberts; S R Pickett; J Massoulié; T L Rosenberry; E Krejci
Journal:  J Biol Chem       Date:  2000-11-03       Impact factor: 5.157

7.  Predicting subcellular localization of proteins based on their N-terminal amino acid sequence.

Authors:  O Emanuelsson; H Nielsen; S Brunak; G von Heijne
Journal:  J Mol Biol       Date:  2000-07-21       Impact factor: 5.469

8.  The evolutionarily conserved trimeric structure of CutA1 proteins suggests a role in signal transduction.

Authors:  Fabio Arnesano; Lucia Banci; Manuela Benvenuti; Ivano Bertini; Vito Calderone; Stefano Mangani; Maria Silvia Viezzoli
Journal:  J Biol Chem       Date:  2003-08-29       Impact factor: 5.157

9.  Structural implications for heavy metal-induced reversible assembly and aggregation of a protein: the case of Pyrococcus horikoshii CutA.

Authors:  Yoshikazu Tanaka; Kouhei Tsumoto; Takeshi Nakanishi; Yoshiaki Yasutake; Naoki Sakai; Min Yao; Isao Tanaka; Izumi Kumagai
Journal:  FEBS Lett       Date:  2004-01-02       Impact factor: 4.124

10.  Molecular genetics of a chromosomal locus involved in copper tolerance in Escherichia coli K-12.

Authors:  S T Fong; J Camakaris; B T Lee
Journal:  Mol Microbiol       Date:  1995-03       Impact factor: 3.501

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  5 in total

1.  Structure of a CutA1 divalent-cation tolerance protein from Cryptosporidium parvum, the protozoal parasite responsible for cryptosporidiosis.

Authors:  Garry W Buchko; Jan Abendroth; Matthew C Clifton; Howard Robinson; Yanfeng Zhang; Stephen N Hewitt; Bart L Staker; Thomas E Edwards; Wesley C Van Voorhis; Peter J Myler
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2015-04-18       Impact factor: 1.056

2.  CutA divalent cation tolerance homolog (Escherichia coli) (CUTA) regulates β-cleavage of β-amyloid precursor protein (APP) through interacting with β-site APP cleaving protein 1 (BACE1).

Authors:  Yingjun Zhao; Yunshu Wang; Jin Hu; Xian Zhang; Yun-Wu Zhang
Journal:  J Biol Chem       Date:  2012-02-17       Impact factor: 5.157

3.  Structure of putative CutA1 from Homo sapiens determined at 2.05 A resolution.

Authors:  Bagautdin Bagautdinov; Yoshinori Matsuura; Svetlana Bagautdinova; Naoki Kunishima; Katsuhide Yutani
Journal:  Acta Crystallogr Sect F Struct Biol Cryst Commun       Date:  2008-04-30

4.  The structures of the CutA1 proteins from Thermus thermophilus and Pyrococcus horikoshii: characterization of metal-binding sites and metal-induced assembly.

Authors:  Bagautdin Bagautdinov
Journal:  Acta Crystallogr F Struct Biol Commun       Date:  2014-03-25       Impact factor: 1.056

5.  Microarray and proteomic analysis of breast cancer cell and osteoblast co-cultures: role of osteoblast matrix metalloproteinase (MMP)-13 in bone metastasis.

Authors:  Charlotte Morrison; Stephanie Mancini; Jane Cipollone; Reinhild Kappelhoff; Calvin Roskelley; Christopher Overall
Journal:  J Biol Chem       Date:  2011-07-22       Impact factor: 5.157

  5 in total

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