Literature DB >> 11527378

The genomic structure and promoter region of the human parkin gene.

S Asakawa1, A Takayanagi, T Sasaki, A Shimizu, A Shintani, K Kawasaki, A J Mungall, S Beck, S Minoshima, N Shimizu.   

Abstract

Parkin has been identified as a causative gene of the autosomal recessive juvenile parkinsonism (AR-JP). In this study, we determined the genomic structure of the Parkin gene and identified a core promoter region based on the DNA sequence of 1.4 Mb. The 5'-flanking region contained no apparent TATA or CAAT box elements but several putative cis-elements for various transcription factors. The GC- and CpG-rich regions were observed not only in the 5'-flanking sequence but also in the 5'-part of the first intron of Parkin. We identified an exact starting point of Parkin transcription. A core promoter region was determined by transfecting a series of deletion constructs with a dual luciferase reporter system into human neuroblastoma cells. Furthermore, we located a neighboring novel gene in a head-to-head direction with Parkin with only a 198-bp interval. Copyright 2001 Academic Press.

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Year:  2001        PMID: 11527378     DOI: 10.1006/bbrc.2001.5490

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


  11 in total

1.  Parkin transcript variants in rat and human brain.

Authors:  Velia Dagata; Sebastiano Cavallaro
Journal:  Neurochem Res       Date:  2004-09       Impact factor: 3.996

2.  A comprehensive analysis of deletions, multiplications, and copy number variations in PARK2.

Authors:  D M Kay; C F Stevens; T H Hamza; J S Montimurro; C P Zabetian; S A Factor; A Samii; A Griffith; J W Roberts; E S Molho; D S Higgins; S Gancher; L Moses; S Zareparsi; P Poorkaj; T Bird; J Nutt; G D Schellenberg; H Payami
Journal:  Neurology       Date:  2010-09-28       Impact factor: 9.910

Review 3.  The genetics of Parkinson disease.

Authors:  Lynn M Bekris; Ignacio F Mata; Cyrus P Zabetian
Journal:  J Geriatr Psychiatry Neurol       Date:  2010-10-11       Impact factor: 2.680

Review 4.  Significance of the parkin gene and protein in understanding Parkinson's disease.

Authors:  Paul S Fishman; George A Oyler
Journal:  Curr Neurol Neurosci Rep       Date:  2002-07       Impact factor: 5.081

5.  Parkin, a gene implicated in autosomal recessive juvenile parkinsonism, is a candidate tumor suppressor gene on chromosome 6q25-q27.

Authors:  Rossano Cesari; Eric S Martin; George A Calin; Francesca Pentimalli; Roberta Bichi; Holly McAdams; Francesco Trapasso; Alessandra Drusco; Masayoshi Shimizu; Valeria Masciullo; Giuseppina D'Andrilli; Giovanni Scambia; Maria Cristina Picchio; Hansjuerg Alder; Andrew K Godwin; Carlo M Croce
Journal:  Proc Natl Acad Sci U S A       Date:  2003-04-28       Impact factor: 11.205

6.  Identification and characterization of a novel endogenous murine parkin mutation.

Authors:  Chenere P Ramsey; Benoit I Giasson
Journal:  J Neurochem       Date:  2010-01-20       Impact factor: 5.372

7.  Midnolin is a novel regulator of parkin expression and is associated with Parkinson's Disease.

Authors:  Yutaro Obara; Toru Imai; Hidenori Sato; Yuji Takeda; Takeo Kato; Kuniaki Ishii
Journal:  Sci Rep       Date:  2017-07-19       Impact factor: 4.379

8.  Generation and characterisation of a parkin-Pacrg knockout mouse line and a Pacrg knockout mouse line.

Authors:  Sarah E M Stephenson; Timothy D Aumann; Juliet M Taylor; Jessica R Riseley; Ruili Li; Jeffrey R Mann; Doris Tomas; Paul J Lockhart
Journal:  Sci Rep       Date:  2018-05-14       Impact factor: 4.379

9.  Mutation Analysis of Consanguineous Moroccan Patients with Parkinson's Disease Combining Microarray and Gene Panel.

Authors:  Ahmed Bouhouche; Christelle Tesson; Wafaa Regragui; Mounia Rahmani; Valérie Drouet; Houyam Tibar; Zouhayr Souirti; Rafiqua Ben El Haj; Naima Bouslam; Mohamed Yahyaoui; Alexis Brice; Ali Benomar; Suzanne Lesage
Journal:  Front Neurol       Date:  2017-10-31       Impact factor: 4.003

10.  Han Chinese family with early-onset Parkinson's disease carries novel compound heterozygous mutations in the PARK2 gene.

Authors:  Ting Huang; Chen-Yu Gao; Liang Wu; Peng-Yu Gong; Ji-Zheng Wang; You-Yong Tian; Ying-Dong Zhang
Journal:  Brain Behav       Date:  2019-08-06       Impact factor: 2.708

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