Literature DB >> 1284470

Identification and developmental expression of the Xenopus laevis cystic fibrosis transmembrane conductance regulator gene.

S J Tucker1, D Tannahill, C F Higgins.   

Abstract

An amphibian homologue of the human cystic fibrosis transmembrane conductance regulator (CFTR) gene has been isolated from Xenopus laevis by polymerase chain reaction (PCR) amplification. The 4455bp sequence encodes a predicted polypeptide of 1485 amino acids which has an overall homology at the amino acid level of 77% identity and 88% similarity with human CFTR. Comparison of these evolutionarily diverse CFTR sequences has structure-function implications. Investigation of the expression of the Xenopus gene during early stages of development (Stages 1-48), using RNAase protection assays and PCR analysis of total Xenopus RNA, shows CFTR mRNA to be present at the very earliest stages of development, including the oocyte and blastula stages, with increasing amounts during subsequent development. The identification of mRNA for a CFTR homologue in the Xenopus oocyte and early stages of development has implications for its biological role.

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Year:  1992        PMID: 1284470     DOI: 10.1093/hmg/1.2.77

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


  16 in total

1.  New nucleotide sequence data on the EMBL File Server.

Authors: 
Journal:  Nucleic Acids Res       Date:  1992-07-25       Impact factor: 16.971

2.  Hypotonicity activates a native chloride current in Xenopus oocytes.

Authors:  M J Ackerman; K D Wickman; D E Clapham
Journal:  J Gen Physiol       Date:  1994-02       Impact factor: 4.086

3.  CFTR: the nucleotide binding folds regulate the accessibility and stability of the activated state.

Authors:  D J Wilkinson; M K Mansoura; P Y Watson; L S Smit; F S Collins; D C Dawson
Journal:  J Gen Physiol       Date:  1996-01       Impact factor: 4.086

4.  Cystic fibrosis transmembrane conductance regulator (CFTR) anion binding as a probe of the pore.

Authors:  M K Mansoura; S S Smith; A D Choi; N W Richards; T V Strong; M L Drumm; F S Collins; D C Dawson
Journal:  Biophys J       Date:  1998-03       Impact factor: 4.033

5.  Molecular cloning of a mammalian ABC transporter homologous to Drosophila white gene.

Authors:  S Savary; F Denizot; M Luciani; M Mattei; G Chimini
Journal:  Mamm Genome       Date:  1996-09       Impact factor: 2.957

6.  An ovine CFTR variant as a putative cystic fibrosis causing mutation.

Authors:  S J Tebbutt; A Harris; D F Hill
Journal:  J Med Genet       Date:  1996-07       Impact factor: 6.318

7.  A hyperpolarization-activated ion current of amphibian oocytes.

Authors:  L D Ochoa-de la Paz; D B Salazar-Soto; J P Reyes; R Miledi; A Martinez-Torres
Journal:  Pflugers Arch       Date:  2013-02-26       Impact factor: 3.657

8.  Four adult patients with the missense mutation L206W and a mild cystic fibrosis phenotype.

Authors:  M Desgeorges; M Rodier; M Piot; J Demaille; M Claustres
Journal:  Hum Genet       Date:  1995-12       Impact factor: 4.132

9.  Identification of three novel mutations (457 TAT-->G, D192G, Q685X) in the Slovenian CF patients.

Authors:  M P Audrézet; N Canki-Klain; B Mercier; D Bracar; C Verlingue; C Férec
Journal:  Hum Genet       Date:  1994-06       Impact factor: 4.132

10.  Retrospective study of the cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations in Guthrie cards from a large cohort of neonatal screening for cystic fibrosis.

Authors:  C Verlingue; B Mercier; I Lecoq; M P Audrézet; D Laroche; G Travert; C Férec
Journal:  Hum Genet       Date:  1994-04       Impact factor: 4.132

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