Cloning the cDNA for a new human zinc finger protein defines a group of closely related krüppel like transcription factors. (1998 Nov)
cloning the cDNA for a new human zinc finger protein defines a group of closely related krüppel like transcription factors . We have identified a novel zinc finger protein that has been named ubiquitous krüppel like factor ( UKLF ) based on structural considerations and the pattern of gene expression . UKLF was isolated by the polymerase chain reaction approach using degenerate oligonucleotides corresponding to the DNA binding domain of erythroid krüppel like factor ( EKLF ) and cDNA prepared from human vascular endothelial cells . The carboxyl terminal portion of UKLF contains three zinc fingers of the Cys2 His2 type and binds in vitro to the caccc motif of the beta globin promoter and to the Sp1 recognition sequence . The amino terminal portion of UKLF consists of a hydrophobic region rich in serines and a negatively charged segment with several glutamic acid residues . The first 47 amino acids of the acidic region are nearly identical to the amino terminal portion of another krüppel like factor , the so called core promoter binding protein ( CPBP ) or Zf9 . Like CPBP / Zf9 , UKLF can function as a transcription activator in co transfection assays . however , this activity is lost when the highly conserved amino terminal segment is deleted . these findings indicate that UKLF and CPBP / Zf9 represent a distinct subgroup of closely related krüppel like activators of transcription . mapping of the UKLF gene to chromosome 2 suggested that UKLF and CPBP …

Zinc finger transcription factors designed for bispecific coregulation of erbb2 and erbb3 receptors : insights into ErbB receptor biology. (2005 Oct)
Zinc finger transcription factors designed for bispecific coregulation of erbb2 and erbb3 receptors : insights into ErbB receptor biology . signaling through the ErbB family of tyrosine kinase receptors in normal and cancer derived cell lines contributes to cell growth and differentiation . In this work , we altered the levels of erbb2 and erbb3 receptors , individually and in combination , by using 6 finger and 12 finger synthetic zinc finger protein artificial transcription factors ( ATFs ) in an epidermoid squamous cell carcinoma line , A431 . We successfully designed 12 finger ATFs capable of coregulating erbb3 and ICAM 1 or erbb2 and erbb3 . With ATFs , the effects of changes in erbb2 and erbb3 receptor levels were evaluated by using cell proliferation , cell migration , and cell signaling assays . Cell proliferation was increased when erbb2 and erbb3 were both overexpressed . Cell migration on collagen was decreased when erbb2 was down regulated , yet migration on laminin was significantly increased with erbb3 overexpression . erbb2 and erbb3 overexpression also stimulated the phosphatidylinositol 3 kinase and mitogen activated protein kinase pathways . Our ATF approach has elucidated differences in ErbB receptor mediated proliferation , migration , and intracellular signaling that cannot be explained merely by the presence or absence of particular ErbB receptors and emphasizes the dynamic nature of the ErbB signaling system . The transcription factor approach developed here provides a gene economical route to the regulation of multiple genes and may be important …

Identification of a novel krueppel related zinc finger gene ( znf184 ) mapping to 6p21. (1997 May)
identification of a novel krueppel related zinc finger gene ( znf184 ) mapping to 6p21 . 3 . cDNA selection and exon trapping were performed on cosmids mapping to a region 3 Mb distal to HLA A . analysis of resulting fragments indicated the presence of two zinc finger transcripts , and one of these was used to isolate a partial cDNA ( znf184 ) from a placental library . The second transcript contained additional sequence of the 5 end of the gene , extending the sequence to 2678 bp . sequence analysis indicates that znf184 is a classical krueppel zinc finger with 19 highly conserved zinc finger motifs at the C terminus and a krueppel associated box at the N terminus of the protein . This gene encodes a 3 . 2 kb transcript that is highly expressed in testis and expressed at a moderate to low level in all other tissues tested . This zinc finger gene maps to a region approximately 200 kb distal to the microsatellite marker d6s105 and approximately 300 kb proximal to d6s1260 .

The biology of the mammalian krüppel like family of transcription factors. (2001 Jan)
The biology of the mammalian krüppel like family of transcription factors . recent advances in molecular cloning have led to the identification of a large number of mammalian zinc finger containing transcription factors that exhibit homology to the drosophila melanogaster protein , krüppel . although the amino acid sequences in the zinc finger domains of these krüppel like factors ( KLFs ) are closely related to one another , the regions outside the zinc fingers of the proteins are usually unique . KLFs display seemingly different and broad biological properties with each functioning as an activator of transcription , a repressor or both . This review article provides a current phylogenetic classification of the identified KLFs to date . More importantly , the currently known biological activities of the KLFs in regulating transcription , cell proliferation , differentiation and development are summarized and compared . further characterization of this interesting protein family should provide additional insights into the their respective regulatory role in various important biological processes .

Genomic organisation and characterisation of the neural sex determination gene fruitless ( fru ) in the hawaiian species drosophila heteroneura. (2000 May)
genomic organisation and characterisation of the neural sex determination gene fruitless ( fru ) in the hawaiian species drosophila heteroneura . there are several mechanisms for the determination of sex . sexual behaviour is part of the sex determination cascade , and in drosophila melanogaster male courtship is controlled in part by the fruitless gene . As part of a study of sexual behaviour in hawaiian drosophila , we have cloned the neural sex determination gene fru from the hawaiian picture wing species drosophila heteroneura . The fru gene has at least seven exons covering a region of 18kb and encodes three transcripts , fruA , fruB and fruC . Each transcript encodes a single ORF of 841 , 678 and 691aa , respectively . The FRUA and FRUB proteins have a BTB protein protein binding domain and two zinc finger like domains and are well conserved with the D . melanogaster proteins . The FRUC protein has a BTB domain but no zinc finger like domains . The fru gene is expressed in 1 7 day old adult males as a 5 . 1kb transcript . This transcript is not seen in adult females , so the fru gene has a different pattern of sex differential expression in the hawaiian drosophila compared with D . melanogaster .

The arabidopsis jagged gene encodes a zinc finger protein that promotes leaf tissue development. (2004 Feb)
The arabidopsis jagged gene encodes a zinc finger protein that promotes leaf tissue development . important goals in understanding leaf development are to identify genes involved in pattern specification , and also genes that translate this information into cell types and tissue structure . Loss of function mutations at the jagged ( JAG ) locus result in arabidopsis plants with abnormally shaped lateral organs including serrated leaves , narrow floral organs , and petals that contain fewer but more elongate cells . jag mutations also suppress bract formation in leafy , apetala1 and apetala2 mutant backgrounds . The JAG gene was identified by map based cloning to be a member of the zinc finger family of plant transcription factors and encodes a protein similar in structure to superman with a single C ( 2 ) H ( 2 ) type zinc finger , a proline rich motif and a short leucine rich repressor motif . JAG mRNA is localized to lateral organ primordia throughout the plant but is not found in the shoot apical meristem . misexpression of JAG results in leaf fusion and the development of ectopic leaf like outgrowth from both vegetative and floral tissues . Thus , JAG is necessary for proper lateral organ shape and is sufficient to induce the proliferation of lateral organ tissue .

The RIM / NIM family of neuronal C2 domain proteins. (2000 Aug)
The RIM / NIM family of neuronal C2 domain proteins . interactions with Rab3 and a new class of Src homology 3 domain proteins . RIM1 is a putative effector protein for rab3s , synaptic GTP binding proteins . RIM1 is localized close to the active zone at the synapse , where it interacts in a GTP dependent manner with Rab3 located on synaptic vesicles . We now describe a second RIM protein , called RIM2 , that is highly homologous to RIM1 and also expressed primarily in brain . Like RIM1 , RIM2 contains an N terminal zinc finger domain that binds to Rab3 as a function of GTP , a central PDZ domain , and two C terminal C ( 2 ) domains that are separated by long alternatively spliced sequences . unexpectedly , the 3 end of the RIM2 gene produces an independent mRNA that encodes a smaller protein referred as NIM2 . NIM2 is composed of a unique N terminal sequence followed by the C terminal part of RIM2 . Data bank searches identified a third RIM / NIM related gene , which encodes a NIM isoform referred to as NIM3 ; no RIM transcript from this gene was detected . To test if NIMs , like RIMs , may function in secretion , we investigated the effect of NIM3 on calcium triggered exocytosis in PC12 cells . NIM3 induced a dramatic increase in calcium evoked exocytosis ( 50 ) , with no significant effect on …

Cloning , genomic organization and promoter activity of the mouse zinc finger protein gene ZF 12 The human zinc finger … (2003 Jun)
cloning , genomic organization and promoter activity of the mouse zinc finger protein gene ZF 12 The human zinc finger protein znf191 is a krüppel like transcription factor , which may be relevant to many diseases such as neuropsychiatric , cardiovascular and liver caner diseases . To elucidate the function of znf191 by gene targeting , it is necessary to clone and characterize of the homologous gene in model organisms ( mice ) . The mouse homologous gene ( ZF 12 ) was cloned and sequenced for the first time , the genbank accession number is ay052495 . It contains four exons and three introns ; all intronic splice sites exhibited consensus GT / AG sequences . The single nucleotide polymorphisms ( SNPs ) in exon 2 and the alternative length of 3 untranslated region ( 3 UTR ) have been found . The linkage of the ZF 12 gene and the zinc finger protein gene Zfp 35 has been found , so the ZF 12 gene can be localized to B3 to C or beside of chromosome 18 . We assessed approximately 1 . 2 kb of 5 flanking region of the ZF 12 gene for basal promoter activity . A series of deletion mutants of 5 flanking region linked to the luciferase gene was constructed . basal level expression of these constructs was tested in COS 7 cells , nih3t3 cells and HeLa cells . By measuring luciferase activity , which was transiently expressed in the transfected cells …

Specific interactions of the autoantigen L7 with multi zinc finger protein ZNF7 and ribosomal protein S7. (1997 Oct)
specific interactions of the autoantigen L7 with multi zinc finger protein ZNF7 and ribosomal protein S7 . The eucaryotic protein L7 , which associates with the large subunit of ribosomes , has been shown to be a major autoantigen in systemic autoimmune arthritis . The N terminus carries a sequence motif that is similar to the leucine zipper domain of eucaryotic transcription factors . This domain promotes the homodimerization of protein L7 through alpha helical coiled coil formation and binds to distinct mrnas , thereby inhibiting their cell free translation . using a yeast two hybrid selection , we have identified from a jurkat T lymphoma cDNA library ribosomal protein S7 and the multi zinc finger protein ZNF7 as proteins that interact with protein L7 . A fragment of L7 carrying the leucine zipper like domain is fully sufficient to mediate these interactions . their potential biological significance is indicated by low apparent dissociation constants of S7 L7 ( 15 x 10 ( 9 ) M ) and , respectively , ZNF7 L7 ( 2 x 10 ( 9 ) M ) complexes and co immunoprecipitation of proteins S7 , ZNF7 , and L7 from a cell lysate with an anti L7 antibody . We also show that ZNF7 like L7 and S7 can exist in a ribosome bound form . This study provides further evidence suggesting that L7 is involved in translational regulation through interactions with components of the translational apparatus .

Combining structure based design with phage display to create new Cys ( 2 ) His ( 2 ) zinc finger … (2000 Oct)
combining structure based design with phage display to create new Cys ( 2 ) His ( 2 ) zinc finger dimers . background : several strategies have been reported for the design and selection of novel DNA binding proteins . Most of these studies have used Cys ( 2 ) His ( 2 ) zinc finger proteins as a framework , and have focused on constructs that bind DNA in a manner similar to zif268 , with neighboring fingers connected by a canonical ( krüppel type ) linker . This linker does not seem ideal for larger constructs because only modest improvements in affinity are observed when more than three fingers are connected in this manner . Two strategies have been described that allow the productive assembly of more than three canonically linked fingers on a DNA site : connecting sets of fingers using linkers ( covalent ) , or assembling sets of fingers using dimerization domains ( non covalent ) . results : using a combination of structure based design and phage display , we have developed a new dimerization system for Cys ( 2 ) His ( 2 ) zinc fingers that allows the assembly of more than three fingers on a desired target site . Zinc finger constructs employing this new dimerization system have high affinity and good specificity for their target sites both in vitro and in vivo . constructs that recognize an asymmetric binding site as heterodimers can be obtained through substitutions in the zinc …

DNA target selectivity by the vitamin D3 receptor : mechanism of dimer binding to an asymmetric repeat element. (1993 Aug)
DNA target selectivity by the vitamin D3 receptor : mechanism of dimer binding to an asymmetric repeat element . The 1 , 25 dihydroxyvitamin D3 receptor , like other members of the nuclear receptor superfamily , forms dimers in solution that are probably stabilized by a dyad symmetrical interface formed by the ligand binding domain . This receptor , however , recognizes DNA targets that are not dyad symmetric but rather are organized as direct repeats of a hexameric sequence with a characteristic 3 bp spacing . using molecular modeling and site directed mutagenesis , we have identified regions within the vitamin D3 receptor zinc finger region that confer selectivity for direct repeats with appropriate spacing . reflecting the organization of the DNA target , these regions , mapping to the tip of the first zinc finger module and the N and C termini of the second finger module , direct asymmetrical protein protein contacts . A stereochemical model is proposed for these interactions .

Mizip , a highly conserved , vertebrate specific melanin concentrating hormone receptor 1 interacting zinc finger protein. (2002 Sep)
mizip , a highly conserved , vertebrate specific melanin concentrating hormone receptor 1 interacting zinc finger protein . using the yeast two hybrid system a novel protein was identified from human brain that interacts with the C terminus of melanin concentrating hormone receptor 1 ( MCH R1 ) . This protein , characterized by a myeloid translocation protein 8 , nervy , deaf1 proteins ( MYND ) zinc finger domain , is termed MCH R1 interacting zinc finger protein , mizip . It is fully conserved in man , rat , mouse and highly conserved in xenopus and zebrafish , but not detectable in invertebrates . mizip gene organization in human ( six exons on chromosome 9q34 . 3 ) and mouse is highly conserved , yet in rodents an additional exon is generated giving rise to alternatively spliced mrnas . mizip is expressed in brain , testis and stomach , where expression of MCH and MCH R1 was previously reported . mizip interaction with MCH R1 was verified by overlay and pull down assays as well as by co transfection experiments in human embryonic kidney 293 cells . mizip is cytoplasmically localized but gets recruited to the plasma membrane when cells are co transfected with MCH R1 supporting the notion that mizip is involved in the function of MCH R1 .

CDNA cloning , DNA binding , and evolution of mammalian transcription factor IIIA. (2002 Jan)
cDNA cloning , DNA binding , and evolution of mammalian transcription factor IIIA . cDNA for rat transcription factor IIIA ( tfiiia ) was cloned by degenerate PCR and rapid amplification of cDNA ends . This cDNA coded for a protein with nine Cys ( 2 ) His ( 2 ) zinc fingers and a non finger C terminal tail ; 63 amino acid ( aa ) sequence identity was observed with the xenopus tfiiia zinc finger region . recombinant rat protein containing only the nine fingers afforded dnase I protection of the identical nucleotides protected by xenopus laevis native tfiiia on the xenopus 5S RNA gene internal control region . A putative mouse tfiiia clone was identified in an expressed sequence tag database by sequence similarity to rat tfiiia . recombinant nine finger protein from this clone afforded dnase I protection of the xenopus 5S rRNA gene like the native frog protein as did a recombinant nine finger form of a putative human tfiiia clone . these DNA binding results demonstrate that these clones code for the respective mammalian tfiiias . rodent and human tfiiias share about 87 aa sequence identity in their zinc finger regions and have evolved to about the same extent as X . laevis and xenopus borealis tfiiias . A monoclonal antibody against human p53 tumor suppressor bound to rat and mouse tfiiia but not to human tfiiia in western blots . The N terminal regions of rodent and human tfiiia do not contain the …

Identification of DNA recognition sequences and protein interaction domains of the multiple Zn finger protein Roaz. (1998 Nov)
identification of DNA recognition sequences and protein interaction domains of the multiple Zn finger protein Roaz . Roaz , a rat C2H2 zinc finger protein , plays a role in the regulation of olfactory neuronal differentiation through its interaction with the Olf 1 / EBF transcription factor family . An additional role for the Roaz / Olf 1 / EBF heterodimeric protein is suggested by its ability to regulate gene activation at a distinct promoter lacking Olf 1 / EBF binding sites . using an in vitro binding site selection assay ( selex ) , we demonstrate that Roaz protein binds to novel inverted perfect or imperfect repeats of gcaccc separated by 2 bp . We show that Roaz is capable of binding to a canonical consensus recognition sequence with high affinity ( Kd 3 nM ) . analysis of the structural requirement for protein dimerization and DNA binding by Roaz reveals the role of specific zinc finger motifs in the Roaz protein for homodimerization and heterodimerization with the Olf 1 / EBF transcription factor . The DNA binding domain of Roaz is mapped to the N terminal 277 amino acids , containing the first seven zinc finger motifs , which confers weak monomeric binding to a single half site and a stronger dimeric binding to the inverted repeat in a binding site dependent manner . Full length protein can form dimers on both the inverted repeat and direct repeat but not on a single half site . these findings …

Metal and DNA binding properties and mutational analysis of the transcription activating factor , B , of coliphage 186 : … (1997 Aug)
metal and DNA binding properties and mutational analysis of the transcription activating factor , B , of coliphage 186 : a prokaryotic C4 zinc finger protein . coliphage 186 B is a 72 amino acid protein belonging to the Ogr family of analogous transcription factors present in P2 like phage , which contain a Cys X2 Cys X22 Cys X4 Cys presumptive zinc finger motif . The molecular characterization of these proteins has been hampered by their insolubility , a difficulty overcome in the present study by obtaining B as a soluble cadmium containing derivative ( CdB ) . atomic absorption spectroscopy showed the presence of one atom of cadmium per molecule of purified CdB . The UV absorption spectrum revealed a shoulder at 250 nm , characteristic of CysS Cd ( II ) ligand to metal charge transfer transitions , and the difference absorption coefficient after acidification ( delta epsilon 248 , 24 mM 1 cm 1 ) indicated the presence of a Cd ( Cys S ) 4 center . Gel mobility shift analysis of CdB with a 186 late promoter demonstrated specific DNA binding ( KD , app 3 4 microm ) and the protein was shown to activate transcription in vitro from a promoter reporter plasmid construct . The B DNA binding site was mapped by gel shift and dnaase I cleavage protection experiments to an area between 70 and 43 relative to the transcription start site , coincident with the consensus sequence , gttgt N8 …

A zinc finger like domain in the 54kda protein of several pestiviruses. (1997 Jul)
A zinc finger like domain in the 54kda protein of several pestiviruses .

Variations of the C2H2 zinc finger motif in the yeast genome and classification of yeast zinc finger proteins. (1997 Jul)
variations of the C2H2 zinc finger motif in the yeast genome and classification of yeast zinc finger proteins . The prosite pattern Zinc finger C2H2 was extended to permit the detection of all C2H2 zinc fingers and their parent proteins in the recently completed sequence of the yeast genome . additionally , a new computer program was written that extracts other zinc binding motifs ( non C2H2 fingers ) , overlapping with the classical zinc finger pattern , from the found set of yeast C2H2 fingers . The complete and correct detection of all fingers is a prerequisite for the classification of the yeast zinc finger proteins in functional terms . The detected 53 yeast C2H2 zinc finger proteins do not contain finger clusters with 10 or more repeats , as is frequently found in higher eukaryotes . Only three proteins contain four or more fingers in a cluster . moreover , nearly all 27 yeast proteins with tandem arrays of two or three finger domains can be classified into nine subgroups with high sequence conservation in their finger clusters , in particular of their DNA recognition helices . these results and application of the recently elaborated finger / DNA recognition rules suggest that the yeast proteins belonging to the same subgroup may recognize identical or very similar DNA sites .

A novel human striated muscle RING zinc finger protein , SMRZ , interacts with smt3b via its RING domain. (2001 Jun)
A novel human striated muscle RING zinc finger protein , SMRZ , interacts with smt3b via its RING domain . The RING domain is a conserved zinc finger motif , which serves as a protein protein interaction interface . searches of a human heart expressed sequence tag data base for genes encoding the RING domain identified a novel cDNA , named striated muscle RING zinc finger protein ( SMRZ ) . The SMRZ cDNA is 1 . 9 kilobase pairs in length and encodes a polypeptide of 288 amino acid residues ; analysis of the peptide sequence demonstrated an N terminal RING domain . fluorescence in situ hybridization localized SMRZ to chromosome 1p33 34 . northern blots demonstrated that SMRZ is expressed exclusively in striated muscle . In the cardiovascular system , SMRZ is more highly expressed in the fetal heart than in the adult heart ( slightly higher expression in the ventricle than in the atrium ) , suggesting that SMRZ is developmentally regulated . SMRZ was found to interact with smt3b , a ubiquitin like protein , through the SMRZ RING domain . This interaction was abolished by mutagenesis of conserved RING domain residues . transient transfection of SMRZ into c2c12 myoblasts showed localization of SMRZ to the nucleus . these data suggest that SMRZ may play an important role in striated muscle cell embryonic development and perhaps in cell cycle regulation .

Znf268 , a novel kruppel like zinc finger protein , is implicated in early human liver development. (2004 Nov)
znf268 , a novel kruppel like zinc finger protein , is implicated in early human liver development . The advancement in gene knockout and transgenesis have brought about enormous improvement in our understanding of mouse embryogenesis in the past decade or so . On the other hand , relatively little is known about human embryogenesis due largely to the lack of easy access to human embryos and tissues for biomedical studies . We have previously isolated a novel zinc finger gene , znf268 , from a 3 week old human embryo cDNA library in an effort to identify genes important for human embryonic development . To investigate the potential involvement of znf268 in human embryogenesis , we report here the spatial and temporal regulation of its expression during development . northern blot and western blot analyses revealed that znf268 is expressed in early embryos , predominantly , if not exclusively , in fetal liver with little detectable expression in other fetal organs . interestingly , unlike most zinc finger proteins , znf268 protein was found to be localized mainly in the cytoplasm of embryonic hepatocytes . This subcellular localization was substantiated by the localization of EGFP znf268 fusion protein overexpressed in the transfected COS7 cells . these results suggest that znf268 plays a role in early human liver development most likely by functioning through a cytoplasmic mechanism .

Characterization of the thermosensitive ts453 reovirus mutant : increased dsrna binding of sigma 3 protein correlates with interferon resistance. (1998 Aug)
characterization of the thermosensitive ts453 reovirus mutant : increased dsrna binding of sigma 3 protein correlates with interferon resistance . The mutation harbored by the reovirus ts453 thermosensitive mutant has been assigned to the S4 gene encoding the major outer capsid protein sigma 3 . previous gene sequencing has identified a nonconservative amino acid substitution located near the zinc finger of sigma 3 protein in the mutant . coexpression in COS cells of the sigma 3 protein presenting this amino acid substitution ( N16K ) , together with the other major capsid protein mu 1 , has also revealed an altered interaction between the two proteins ; this altered interaction prevents the sigma 3 dependent cleavage of mu 1 to mu 1C . This could explain the lack of outer capsid assembly observed during ts453 virus infection at nonpermissive temperature . In the present study , we pursued the characterization of this mutant sigma 3 protein . although the N16K mutation is located close to the zinc finger region , it did not affect the ability of the protein to bind zinc . In contrast , this mutation , as well as mutations within the zinc finger motif itself , can increase the binding of the protein to double stranded RNA ( dsrna ) . It also appears that the N16K mutant protein is more efficiently transported to the nucleus than the wild type protein , an observation consistent with the postulated role of dsrna binding in sigma 3 nuclear …