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1.
Magn Reson Med ; 64(4): 929-38, 2010 Oct.
Article in English | MEDLINE | ID: mdl-20740664

ABSTRACT

In the present study, a chemical shift saturation recovery method in hyperpolarized (129)Xe MR spectroscopy measurements was applied to two groups of spontaneously breathing mice, an elastase-induced emphysema model and a control group. Parameters detected were those related to lung structures and functions, such as alveolar septal thickness, h, the ratio of the alveolar septal volume relative to gas space volume, V(s)/V(a), and the transit time of blood through the gas exchange region, τ. To investigate the potential of these parameters as biomarkers, an attempt was made to detect physiologic changes in the lungs of elastase-treated mice. Our results showed that V(s)/V(a) was significantly reduced in elastase-treated mice, reflecting emphysema-like destruction of the alveolar wall. Compared with histologic results, this degree of reduction was shown to reflect the severity of wall destruction. On the other hand, significant changes in other parameters, h and τ, were not shown. This study is the first application of hyperpolarized (129)Xe MR spectroscopy to a mouse model of emphysema and shows that the V(s)/V(a) volume ratio is an effective biomarker for emphysema that could become useful in drug research and development through noninvasive detection of pathologic changes in small rodents.


Subject(s)
Disease Models, Animal , Lung/metabolism , Magnetic Resonance Spectroscopy/methods , Pulmonary Emphysema/diagnosis , Pulmonary Emphysema/metabolism , Xenon Isotopes/pharmacokinetics , Animals , Humans , Male , Mice , Mice, Inbred Strains , Radiopharmaceuticals , Reproducibility of Results , Sensitivity and Specificity
2.
Proc Natl Acad Sci U S A ; 104(16): 6834-9, 2007 Apr 17.
Article in English | MEDLINE | ID: mdl-17426146

ABSTRACT

Vocal learning and neuronal replacement have been studied extensively in songbirds, but until recently, few molecular and genomic tools for songbird research existed. Here we describe new molecular/genomic resources developed in our laboratory. We made cDNA libraries from zebra finch (Taeniopygia guttata) brains at different developmental stages. A total of 11,000 cDNA clones from these libraries, representing 5,866 unique gene transcripts, were randomly picked and sequenced from the 3' ends. A web-based database was established for clone tracking, sequence analysis, and functional annotations. Our cDNA libraries were not normalized. Sequencing ESTs without normalization produced many developmental stage-specific sequences, yielding insights into patterns of gene expression at different stages of brain development. In particular, the cDNA library made from brains at posthatching day 30-50, corresponding to the period of rapid song system development and song learning, has the most diverse and richest set of genes expressed. We also identified five microRNAs whose sequences are highly conserved between zebra finch and other species. We printed cDNA microarrays and profiled gene expression in the high vocal center of both adult male zebra finches and canaries (Serinus canaria). Genes differentially expressed in the high vocal center were identified from the microarray hybridization results. Selected genes were validated by in situ hybridization. Networks among the regulated genes were also identified. These resources provide songbird biologists with tools for genome annotation, comparative genomics, and microarray gene expression analysis.


Subject(s)
Brain/embryology , Finches/genetics , Gene Expression Regulation, Developmental/physiology , Genomics/methods , Animals , Brain/growth & development , Brain/metabolism , Brain Chemistry/genetics , Brain Chemistry/physiology , Canaries/embryology , Canaries/genetics , Canaries/growth & development , Canaries/metabolism , Chickens , Cloning, Molecular , Expressed Sequence Tags , Finches/embryology , Finches/growth & development , Finches/metabolism , Gene Library , Humans , Male , Mice , MicroRNAs/analysis , Molecular Sequence Data , Oligonucleotide Array Sequence Analysis , Sequence Analysis, DNA
3.
J Mol Biol ; 353(1): 138-54, 2005 Oct 14.
Article in English | MEDLINE | ID: mdl-16154587

ABSTRACT

The large beta and beta' subunits of the bacterial core RNA polymerase (RNAP) are highly conserved throughout evolution. Nevertheless, large sequence insertions in beta and beta' characterize specific evolutionary lineages of bacteria. The Thermus aquaticus RNAP beta' subunit contains a 283 residue insert between conserved regions A and B that is found in only four bacterial species. The Escherichia coli RNAP beta' subunit contains a 188 residue insert in the middle of conserved region G that is found in a wide range of bacterial species. Here, we present structural studies of these two beta' insertions. We show that the inserts comprise repeats of a previously characterized fold, the sandwich-barrel hybrid motif (as predicted from previous sequence analysis) and that the inserts serve significant roles in facilitating protein/protein and/or protein/nucleic acid interactions.


Subject(s)
DNA-Directed RNA Polymerases/chemistry , DNA-Directed RNA Polymerases/metabolism , Amino Acid Sequence , Crystallography, X-Ray , DNA-Directed RNA Polymerases/genetics , Holoenzymes/chemistry , Holoenzymes/genetics , Holoenzymes/metabolism , Models, Molecular , Molecular Sequence Data , Protein Structure, Quaternary , Protein Structure, Tertiary , Sequence Homology, Amino Acid
4.
J Mol Biol ; 340(5): 941-56, 2004 Jul 23.
Article in English | MEDLINE | ID: mdl-15236958

ABSTRACT

Cell type-specific transcription during Bacillus sporulation is established by sigma(F), the activity of which is controlled by a regulatory circuit involving the anti-sigma factor and serine kinase SpoIIAB, and the anti-anti-sigma SpoIIAA. When ATP is present in the nucleotide-binding site of SpoIIAB, SpoIIAA is phosphorylated, followed by dissociation. The nucleotide-binding site of SpoIIAB is left bound to ADP. SpoIIAB(ADP) can bind an unphosphorylated molecule of SpoIIAA as a stable binding partner. Thus, in this circuit, SpoIIAA plays a dual role as a substrate of the SpoIIAB kinase activity, as well as a tight binding inhibitor. Crystal structures of both the pre-phosphorylation complex and the inhibitory complex, SpoIIAB(ATP) and SpoIIAB(ADP) bound to SpoIIAA, respectively, have been determined. The structural differences between the two forms are subtle and confined to interactions with the phosphoryl groups of the nucleotides. The structures reveal details of the SpoIIAA:SpoIIAB interactions and how phosphorylated SpoIIAA dissociates from SpoIIAB(ADP). Finally, the results confirm and expand upon the docking model for SpoIIAA function as an anti-anti-sigma in releasing sigma(F) from SpoIIAB.


Subject(s)
Adenosine Diphosphate/metabolism , Adenosine Triphosphate/metabolism , Bacillus/chemistry , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Sigma Factor/antagonists & inhibitors , Bacterial Proteins/antagonists & inhibitors , Catalysis , Crystallization , Crystallography, X-Ray , Models, Molecular , Protein Binding , Protein Structure, Tertiary , Static Electricity
6.
Science ; 296(5571): 1280-4, 2002 May 17.
Article in English | MEDLINE | ID: mdl-12016306

ABSTRACT

The crystal structure of the initiating form of Thermus aquaticus RNA polymerase, containing core RNA polymerase (alpha2betabeta'omega) and the promoter specificity sigma subunit, has been determined at 4 angstrom resolution. Important structural features of the RNA polymerase and their roles in positioning sigma within the initiation complex are delineated, as well as the role played by sigma in modulating the opening of the RNA polymerase active-site channel. The two carboxyl-terminal domains of sigma are separated by 45 angstroms on the surface of the RNA polymerase, but are linked by an extended loop. The loop winds near the RNA polymerase active site, where it may play a role in initiating nucleotide substrate binding, and out through the RNA exit channel. The advancing RNA transcript must displace the loop, leading to abortive initiation and ultimately to sigma release.


Subject(s)
DNA-Directed RNA Polymerases/chemistry , DNA-Directed RNA Polymerases/metabolism , Thermus/enzymology , Transcription, Genetic , Amino Acid Motifs , Binding Sites , Crystallization , Crystallography, X-Ray , DNA, Bacterial/metabolism , Eukaryotic Cells/metabolism , Holoenzymes/chemistry , Holoenzymes/metabolism , Models, Molecular , Promoter Regions, Genetic , Protein Conformation , Protein Structure, Quaternary , Protein Structure, Secondary , Protein Structure, Tertiary , RNA, Bacterial/metabolism , RNA, Messenger/metabolism , Sigma Factor/metabolism
7.
Science ; 296(5571): 1285-90, 2002 May 17.
Article in English | MEDLINE | ID: mdl-12016307

ABSTRACT

The crystal structure of Thermus aquaticus RNA polymerase holoenzyme (alpha2betabeta'omegasigmaA) complexed with a fork-junction promoter DNA fragment has been determined by fitting high-resolution x-ray structures of individual components into a 6.5-angstrom resolution map. The DNA lies across one face of the holoenzyme, completely outside the RNA polymerase active site channel. All sequence-specific contacts with core promoter elements are mediated by the sigma subunit. A universally conserved tryptophan is ideally positioned to stack on the exposed face of the base pair at the upstream edge of the transcription bubble. Universally conserved basic residues of the sigma subunit provide critical contacts with the DNA phosphate backbone and play a role in directing the melted DNA template strand into the RNA polymerase active site. The structure explains how holoenzyme recognizes promoters containing variably spaced -10 and -35 elements and provides the basis for models of the closed and open promoter complexes.


Subject(s)
DNA, Bacterial/chemistry , DNA-Directed RNA Polymerases/chemistry , Promoter Regions, Genetic , Sigma Factor/chemistry , Thermus/enzymology , Transcription, Genetic , Base Sequence , Binding Sites , Crystallization , Crystallography, X-Ray , DNA, Bacterial/genetics , DNA, Bacterial/metabolism , DNA-Directed RNA Polymerases/metabolism , Holoenzymes/chemistry , Holoenzymes/metabolism , Models, Molecular , Nucleic Acid Conformation , Protein Conformation , Protein Structure, Quaternary , Protein Structure, Secondary , Protein Subunits , Sigma Factor/metabolism , Templates, Genetic
8.
Cell ; 108(6): 795-807, 2002 Mar 22.
Article in English | MEDLINE | ID: mdl-11955433

ABSTRACT

Cell type-specific transcription during Bacillus sporulation is established by sigmaF. SpoIIAB is an anti-sigma that binds and negatively regulates sigmaF, as well as a serine kinase that phosphorylates and inactivates the anti-anti-sigma SpoIIAA. The crystal structure of sigmaF bound to the SpoIIAB dimer in the low-affinity, ADP form has been determined at 2.9 A resolution. SpoIIAB adopts the GHKL superfamily fold of ATPases and histidine kinases. A domain of sigmaF contacts both SpoIIAB monomers, while 80% of the sigma factor is disordered. The interaction occludes an RNA polymerase binding surface of sigmaF, explaining the SpoIIAB anti-sigma activity. The structure also explains the specificity of SpoIIAB for its target sigma factors and, in combination with genetic and biochemical data, provides insight into the mechanism of SpoIIAA anti-anti-sigma activity.


Subject(s)
Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Geobacillus stearothermophilus/chemistry , Sigma Factor/chemistry , Sigma Factor/metabolism , Transcription Factors , Adenosine Triphosphate/metabolism , Binding Sites , Catalytic Domain , Crystallography , Dimerization , Molecular Sequence Data , Protein Structure, Secondary , Protein Structure, Tertiary , Sequence Homology, Amino Acid , Sigma Factor/antagonists & inhibitors , Spores, Bacterial/chemistry
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