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1.
Anal Sci ; 20(2): 311-4, 2004 Feb.
Article in English | MEDLINE | ID: mdl-15055957

ABSTRACT

Zirconium oxy-salts were hydrolyzed to form positively charged polymer or cluster species in acidic solutions. The zirconium hydrolyzed polymer was found to react with a negatively charged polyelectrolyte, such as poly(vinyl sulfate), and to form a stoichiometric polyion complex. Thus, colloidal titration with poly(vinyl sulfate) was applied to measure the zirconium concentration in an acidic solution by using a Toluidine Blue selective plasticized poly(vinyl chloride) membrane electrode as a potentiometric end-point detecting device. The determination could be performed with 1% of the relative standard deviation. The colloidal titration stoichiometry at pH < or = 2 was one mol of zirconium per equivalent mol of poly(vinyl sulfate).

2.
Physiol Genomics ; 11(2): 91-8, 2002 Oct 29.
Article in English | MEDLINE | ID: mdl-12388799

ABSTRACT

Vertebrate hematopoiesis is regulated by distinct cell-specific transcription factors such as GATA-1 and SCL. Mammalian p45-NFE2 was characterized for its ability to bind the hypersensitive sites of the globin locus control region. NFE2 is a member of a cap'n'collar (CNC) and basic zipper (BZIP) superfamily that regulates gene transcription. It has been implicated in diverse processes such as globin gene expression, oxidative stress, and platelet lineage differentiation. Here, we have isolated the zebrafish ortholog of NFE2. The gene is highly homologous, particularly in the DNA-binding domain. Mapping the zebrafish NFE2 to linkage group 23 establishes a region of chromosomal synteny with human chromosome 12, further suggesting evolutionary conservation. During embryogenesis, the zebrafish gene is expressed specifically in erythroid cells and also in the developing ear. NFE2 expression is lacking in zebrafish mutants that have no hematopoietic cells. An analysis of the sauternes mutant, which carries a mutation in the ALAS-2 gene and thus has defective heme synthesis, demonstrates higher levels of NFE2 expression than normal. This further establishes the block to erythroid differentiation in the sauternes mutant. Our studies demonstrate conservation of the vertebrate genetic program for the erythroid lineage.


Subject(s)
DNA-Binding Proteins/chemistry , DNA-Binding Proteins/genetics , Transcription Factors/chemistry , Transcription Factors/genetics , Zebrafish/genetics , Animals , Base Sequence , Chromosomes, Human, Pair 21/genetics , Erythroid-Specific DNA-Binding Factors , GATA1 Transcription Factor , Gene Expression Profiling/methods , Gene Expression Regulation, Developmental/genetics , Humans , Kidney/chemistry , Molecular Sequence Data , Mutation/genetics , NF-E2 Transcription Factor, p45 Subunit , Synteny/genetics , Zebrafish Proteins/chemistry , Zebrafish Proteins/genetics
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