Literature DB >> 14767562

Identification and characterization of Crumbs homolog 2 gene at human chromosome 9q33.3.

Masuko Katoh1, Masaru Katoh.   

Abstract

Drosophila Crumbs (Crb)--Stardust (Sdt)--Discs lost (Dlt) complex plays a pivotal role in the establishment and the maintenance of epithelial polarity. CRB1 and CRB3 are human homologs of Drosophila Crb, MPP1-MPP7 are human homologs of Drosophila Sdt, INADL/PATJ and MPDZ/MUPP1 are human homologs of Drosophila Dlt. Here, we identified and characterized a novel Crumbs family gene, Crumbs homolog 2 (CRB2), by using bioinformatics. CRB2 isoform 1 was assembled by adding nucleotide position 1-3353 of FLJ16786 cDNA (AK123000) to the 5'-end of 5'-truncated FLJ38464 cDNA (NM_173689.1), while that of CRB2 isoform 2 was derived from FLJ16786 cDNA. CRB2 isoform 1, consisting of exon 1-13, encoded a 1285-aa transmembrane protein. CRB2 isoform 2, consisting of exon 1-10 and intron 10, encoded a 1176-aa secreted protein. CRB2 gene was found to encode transmembrane protein as well as secreted protein due to alternative splicing. CRB2 isoform 1, showing 24.4% total amino-acid identity with CRB1, was type I transmembrane protein with 14 extracellular EGF-like domains, 3 extracellular Laminin G-like domains and the Crb cytoplasmic tail (CCT) domain. CCT domain, functioning as the binding site for PDZ domain of Sdt homologs, was conserved among human CRB1, CRB2, CRB3, mouse Crb1, Crb3, Drosophila Crb, and C. elegans crb. Comparative genomics revealed that CRB2-KIAA1608-LHX2-NEK6 locus at human chromosome 9q33.3 and CRB1-MGC27044-LHX9-NEK7 locus at human chromosome 1q31.3 were paralogous regions within the human genome. This is the first report on identification and characterization of the CRB2 gene.

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Year:  2004        PMID: 14767562

Source DB:  PubMed          Journal:  Int J Oncol        ISSN: 1019-6439            Impact factor:   5.650


  12 in total

Review 1.  Cross talk between the Crumbs complex and Hippo signaling in renal epithelial cells.

Authors:  U Michgehl; H Pavenstädt; B Vollenbröker
Journal:  Pflugers Arch       Date:  2017-06-13       Impact factor: 3.657

2.  CRB2 mutations produce a phenotype resembling congenital nephrosis, Finnish type, with cerebral ventriculomegaly and raised alpha-fetoprotein.

Authors:  Anne Slavotinek; Julie Kaylor; Heather Pierce; Michelle Cahr; Stephanie J DeWard; Dina Schneidman-Duhovny; Adnan Alsadah; Fadi Salem; Gabriela Schmajuk; Lakshmi Mehta
Journal:  Am J Hum Genet       Date:  2014-12-31       Impact factor: 11.025

3.  The connecdenn family, Rab35 guanine nucleotide exchange factors interfacing with the clathrin machinery.

Authors:  Andrea L Marat; Peter S McPherson
Journal:  J Biol Chem       Date:  2010-02-12       Impact factor: 5.157

4.  Nok plays an essential role in maintaining the integrity of the outer nuclear layer in the zebrafish retina.

Authors:  Xiangyun Wei; Jian Zou; Masaki Takechi; Shoji Kawamura; Lihua Li
Journal:  Exp Eye Res       Date:  2006-03-10       Impact factor: 3.467

Review 5.  Apico-basal polarity complex and cancer.

Authors:  Mohammed Khursheed; Murali Dharan Bashyam
Journal:  J Biosci       Date:  2014-03       Impact factor: 1.826

Review 6.  Expansion of phenotype and genotypic data in CRB2-related syndrome.

Authors:  Ryan E Lamont; Wen-Hann Tan; A Micheil Innes; Jillian S Parboosingh; Dina Schneidman-Duhovny; Aleksandar Rajkovic; John Pappas; Pablo Altschwager; Stephanie DeWard; Anne Fulton; Kathryn J Gray; Max Krall; Lakshmi Mehta; Lance H Rodan; Devereux N Saller; Deanna Steele; Deborah Stein; Svetlana A Yatsenko; François P Bernier; Anne M Slavotinek
Journal:  Eur J Hum Genet       Date:  2016-03-23       Impact factor: 4.246

7.  Defects of CRB2 cause steroid-resistant nephrotic syndrome.

Authors:  Lwaki Ebarasi; Shazia Ashraf; Agnieszka Bierzynska; Heon Yung Gee; Hugh J McCarthy; Svjetlana Lovric; Carolin E Sadowski; Werner Pabst; Virginia Vega-Warner; Humphrey Fang; Ania Koziell; Michael A Simpson; Ismail Dursun; Erkin Serdaroglu; Shawn Levy; Moin A Saleem; Friedhelm Hildebrandt; Arindam Majumdar
Journal:  Am J Hum Genet       Date:  2014-12-31       Impact factor: 11.025

8.  A case report of CRB2 mutation identified in a Chinese boy with focal segmental glomerulosclerosis.

Authors:  Jiaojiao Fan; Rong Fu; Fuxian Ren; Junjie He; Shujing Wang; Mengfan Gou
Journal:  Medicine (Baltimore)       Date:  2018-09       Impact factor: 1.817

9.  Loss of Crb2b-lf leads to anterior segment defects in old zebrafish.

Authors:  Satu Kujawski; Cátia Crespo; Marta Luz; Michaela Yuan; Sylke Winkler; Elisabeth Knust
Journal:  Biol Open       Date:  2020-02-11       Impact factor: 2.422

10.  Crumbs2 mediates ventricular layer remodelling to form the spinal cord central canal.

Authors:  Christine M Tait; Kavitha Chinnaiya; Elizabeth Manning; Mariyam Murtaza; John-Paul Ashton; Nicholas Furley; Chris J Hill; C Henrique Alves; Jan Wijnholds; Kai S Erdmann; Andrew Furley; Penny Rashbass; Raman M Das; Kate G Storey; Marysia Placzek
Journal:  PLoS Biol       Date:  2020-03-09       Impact factor: 8.029

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