Literature DB >> 12951058

Expression analysis of the human adducin gene family and evidence of ADD2 beta4 multiple splicing variants.

Lorena Citterio1, Laura Tizzoni, Marco Catalano, Gianpaolo Zerbini, Giuseppe Bianchi, Cristina Barlassina.   

Abstract

Adducin is a cytoskeleton heterodimeric protein. Its subunits are encoded by three related genes (ADD1, ADD2, and ADD3) which show alternative spliced variants. Adducin polymorphisms are involved in blood pressure regulation in humans and rats. We have analyzed mRNA distribution of ADD gene family in human tissues and cells with Real-Time TaqMan RT-PCR. Whereas ADD1 is ubiquitously distributed, ADD3 is more expressed in kidney medulla and cortex than in fetal kidney, while in adult liver it is less abundant than in fetal liver. ADD2 beta1 and beta4 variants show the same pattern of distribution with the highest expression in brain, fetal liver, and kidney. Conventional RT-PCR identified new beta4 variants. Beta4a is characterized by an in-frame insertion of 21 nucleotides upstream exon 15 predicting a 7 amino acids longer protein with a similar C-terminus region. It is coexpressed with beta1 and beta4 in several tissues. Fetal kidney shows further beta4b, beta4c and beta4d variants containing internal exon deletions that enormously modify the predicted NH(2) and central regions. Our findings could help one to understand the functional role of adducin variants in specific tissues and cells.

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Year:  2003        PMID: 12951058     DOI: 10.1016/j.bbrc.2003.08.011

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


  6 in total

1.  A role for α-adducin (ADD-1) in nematode and human memory.

Authors:  Vanja Vukojevic; Leo Gschwind; Christian Vogler; Philippe Demougin; Dominique J-F de Quervain; Andreas Papassotiropoulos; Attila Stetak
Journal:  EMBO J       Date:  2012-02-03       Impact factor: 11.598

2.  Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

Authors:  Maria-Mercè Garcia-Barceló; Ming-Yiu Yeung; Xiao-Ping Miao; Clara Sze-Man Tang; Guo Cheng; Guo Chen; Man-Ting So; Elly Sau-Wai Ngan; Vincent Chi-Hang Lui; Yan Chen; Xue-Lai Liu; Kenneth-Jeremy W S Hui; Long Li; Wei-Hong Guo; Xiao-Bin Sun; Jin-Fa Tou; Kin-Wai Chan; Xuan-Zhao Wu; You-Qiang Song; Danny Chan; Kenneth Cheung; Patrick Ho-Yu Chung; Kenneth Kak-Yuen Wong; Pak-Chung Sham; Stacey S Cherny; Paul Kwong-Hang Tam
Journal:  Hum Mol Genet       Date:  2010-05-11       Impact factor: 6.150

3.  Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.

Authors:  Ellen A Tsai; Christopher M Grochowski; Kathleen M Loomes; Kazuhiko Bessho; Hakon Hakonarson; Jorge A Bezerra; Pierre A Russo; Barbara A Haber; Nancy B Spinner; Marcella Devoto
Journal:  Hum Genet       Date:  2013-10-09       Impact factor: 4.132

4.  Whole exome sequencing analysis for mutations in isolated type III biliary atresia patients.

Authors:  Kubilay Gürünlüoğlu; Ahmet Koç; Kübra Durmuş; Harika Gözükara Bağ; Canan Ceran; Semra Gürünlüoğlu; Turan Yıldız; Mehmet Gül; Mehmet Demircan
Journal:  Clin Exp Hepatol       Date:  2020-12-30

5.  Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish.

Authors:  Vivian Tang; Zenobia C Cofer; Shuang Cui; Valerie Sapp; Kathleen M Loomes; Randolph P Matthews
Journal:  J Pediatr Gastroenterol Nutr       Date:  2016-11       Impact factor: 2.839

6.  Downregulation of microRNA-145 may contribute to liver fibrosis in biliary atresia by targeting ADD3.

Authors:  Yongqin Ye; Zhihan Li; Qi Feng; Zimin Chen; Zhouguang Wu; Jianyao Wang; Xiaoshuo Ye; Dahao Zhang; Lei Liu; Wei Gao; Lihui Zhang; Bin Wang
Journal:  PLoS One       Date:  2017-09-13       Impact factor: 3.240

  6 in total

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