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1.
Genomics ; 71(3): 282-95, 2001 Feb 01.
Article in English | MEDLINE | ID: mdl-11170745

ABSTRACT

The genome organization of the human major histocompatibility complex (MHC) will be best understood in a comparative evolutionary context. We describe here the construction of a physical map for the feline MHC. A large-insert domestic cat genomic DNA library was developed using a P1 artificial chromosome (PAC) with a genomic representation of 2.5x and an average insert size of 80 kb. A sequence-ready 660-kb bacterial artificial chromosome/PAC contig map of the domestic cat MHC class II region was constructed with a gene order similar to, but distinct from, that of human and mice: DPB/DPA, Ring3, DMB, TAP1, DOB, DRB2, DRA3, DRB1, DRA2, and DRA1. Fluorescence in situ hybridization analyses of selected class II PAC clones confirmed that the class II region lies in the pericentromeric region of cat chromosome B2. However, apparently unlike the human and mouse MHCs, the domestic cat DRA and DRB genes have undergone multiple duplications and the DQ region has been deleted.


Subject(s)
Cats/genetics , Chromosomes, Artificial, Bacterial , Contig Mapping , Genes, MHC Class II , Genome , Animals , Blotting, Southern , Chromosome Mapping , Chromosomes , DNA Restriction Enzymes/metabolism , Fibroblasts/metabolism , Gene Library , HLA-DP Antigens/genetics , HLA-DR Antigens/genetics , Humans , In Situ Hybridization, Fluorescence , Male , Mice , Models, Genetic , Nucleic Acid Hybridization , Oligonucleotide Probes/metabolism
2.
Cytogenet Cell Genet ; 95(3-4): 210-24, 2001.
Article in English | MEDLINE | ID: mdl-12063402

ABSTRACT

Canidae species fall into two categories with respect to their chromosome composition: those with high numbered largely acrocentric karyotypes and others with a low numbered principally metacentric karyotype. Those species with low numbered metacentric karyotypes are derived from multiple independent fusions of chromosome segments found as acrocentric chromosomes in the high numbered species. Extensive chromosome homology is apparent among acrocentric chromosome arms within Canidae species; however, little chromosome arm homology exists between Canidae species and those from other Carnivore families. Here we use Zoo-FISH (fluorescent in situ hybridization, also called chromosomal painting) probes from flow-sorted chromosomes of the Japanese raccoon dog (Nyctereutes procyonoides) to examine two phylogenetically divergent canids, the arctic fox (Alopex lagopus) and the crab-eating fox (Cerdocyon thous). The results affirm intra-canid chromosome homologies, also implicated by G-banding. In addition, painting probes from domestic cat (Felis catus), representative of the ancestral carnivore karyotype (ACK), and giant panda (Ailuropoda melanoleuca) were used to define primitive homologous segments apparent between canids and other carnivore families. Canid chromosomes seem unique among carnivores in that many canid chromosome arms are mosaics of two to four homology segments of the ACK chromosome arms. The mosaic pattern apparently preceded the divergence of modern canid species since conserved homology segments among different canid species are common, even though those segments are rearranged relative to the ancestral carnivore genome arrangement. The results indicate an ancestral episode of extensive centric fission leading to an ancestral canid genome organization that was subsequently reorganized by multiple chromosome fusion events in some but not all Canidae lineages.


Subject(s)
Carnivora/genetics , Chromosomes/genetics , Phylogeny , Animals , Cats , Chromosome Banding , Chromosome Painting , DNA Probes , Foxes , Genome , Male , Ursidae
3.
Alcohol Clin Exp Res ; 24(6): 810-21, 2000 Jun.
Article in English | MEDLINE | ID: mdl-10888069

ABSTRACT

BACKGROUND: There is compelling evidence that genetic factors play a major role in the development of alcohol dependence. Platelet adenylyl cyclase (AC) activity has been proposed as a biochemical marker for differentiating alcohol-dependent and nondependent subjects, but the sensitivity and specificity of this marker have not been ascertained. The objective of this study was to determine the sensitivity and specificity of platelet AC activity in identifying alcohol-dependent subjects and to ascertain the effect of medical/ psychiatric variables, drinking and smoking history, and age and body weight on AC activity. METHODS: The cross-sectional study was conducted from 1995 to 1998. Participants were 210 Australian White men who were community volunteers and alcohol treatment inpatients in Sydney, Australia. There were 41 nondrinkers, 140 drinkers, and 29 men who were entering alcohol treatment. The main outcome measure was platelet AC activity. Classification variables were plasma ethanol, gamma-glutamyltransferase, aspartate aminotransferase, serum carbohydrate-deficient transferrin (CDT), and urinary 5-hydroxytryptophol/5-hydroxyindoleacetic acid (5-HTOL/5-HIAA) levels, and World Health Organization/International Society for Biomedical Research on Alcoholism Interview Schedule variables, which included alcohol use and dependence criteria. RESULTS: Among subjects who reported abstinence for at least 4 days, both cesium fluoride (CsF)- and forskolin-stimulated platelet AC activities were significantly lower in those with a lifetime history of alcohol dependence compared with those with no such history (p < 0.005 and p < 0.05, respectively). The sensitivity and specificity of CsF-stimulated AC activity to discriminate individuals with a lifetime history of alcohol dependence were 75% and 79%, respectively. Similar values for sensitivity and specificity for CsF-stimulated AC activity were calculated when discriminating current alcohol dependence in the subjects in our sample. Irrespective of the history of alcohol dependence, persons who had consumed alcohol recently (within the last 3-4 days) showed significantly higher mean basal, CsF-stimulated, and forskolin-stimulated AC activity (p < 0.001), as did those who had elevated 5-HTOL/5-HIAA ratios or CDT levels, indicative of recent (heavy) drinking. The "normalization" of platelet AC activity to baseline levels after an individual stops drinking may be related to the generation of new platelets during the abstinence period. Conduct disorder and antisocial personality disorder were not associated with low AC activity, but low forskolin-stimulated AC activity was associated with major depression. CONCLUSIONS: We found that CsF- and forskolin-stimulated platelet AC activity discriminates between subjects with and without alcohol dependence in a population of subjects who had not consumed significant quantities of ethanol recently. Recent alcohol consumption is a confounding variable that can alter the measured levels of AC activity. Forskolin-stimulated platelet AC activity also may be influenced by a history of major depression.


Subject(s)
Adenylyl Cyclases/blood , Alcoholism/enzymology , Blood Platelets/enzymology , Temperance , Adenylyl Cyclases/drug effects , Adult , Alcoholism/genetics , Alcoholism/metabolism , Analysis of Variance , Australia/epidemiology , Biomarkers/blood , Blood Platelets/drug effects , Colforsin/pharmacology , Cross-Sectional Studies , Humans , Hyperlipidemias/blood , Male , Middle Aged
5.
Biotechniques ; 27(3): 608-13, 1999 Sep.
Article in English | MEDLINE | ID: mdl-10489619

ABSTRACT

Tyramide signal amplification (TSA)-FISH was used to map one mouse and two human DNA probes of less than 1 kb in size. The two human probes were 319 and 608 bp, and the mouse probe was 855 bp. Probes, made from PCR products, were labeled by incorporating biotin-11-dUTP (human) and biotin-16-dUTP (mouse) during PCR amplification. Signals were readily observed in both interphase and metaphase cells following TSA-FISH for all three genes, whereas conventional FISH experiments produced no signals. The two human ATP-binding cassette (ABC) genes, EST883227 (GenBank Accession No. AA243820) and EST990006 (GenBank Accession No. AA348546), mapped to human chromosomes 7p21 and 17q25. The mouse gene, cmyc (exon 2) mapped to band D2 of mouse chromosome 15. These findings demonstrate the ability of this technique to map small probes (PCR products and expressed sequence tags) of less than 1 kb through highly increased signal amplification.


Subject(s)
Biotin/analogs & derivatives , Chromosome Mapping , DNA Probes , In Situ Hybridization, Fluorescence/methods , Polymerase Chain Reaction , Tyramine/analogs & derivatives , Animals , Chromosomes, Human, Pair 17 , Chromosomes, Human, Pair 7 , Deoxyuracil Nucleotides , Genes, myc/genetics , Humans , Lymphocytes/ultrastructure , Mice , Spleen/ultrastructure
6.
Alcohol Clin Exp Res ; 22(5): 1057-64, 1998 Aug.
Article in English | MEDLINE | ID: mdl-9726273

ABSTRACT

Low platelet adenylyl cyclase (AC) activity has been previously proposed to be a trait marker reflecting a genetic predisposition to alcohol dependence. To determine whether low platelet AC activity in alcohol-dependent subjects may be related to specific diagnostic criteria of DSM-IV and ICD-10 alcohol use disorders, we analyzed responses obtained in structured clinical interviews of 36 subjects who were determined to be alcohol-dependent Platelet AC activity when stimulated by guanylyl-imidodiphosphate [Gpp(NH)p] or forskolin was significantly lower in alcohol-dependent subjects as a group, compared with controls. When we analyzed the responses of the alcohol-dependent subjects to questions used to establish the diagnosis of alcohol abuse/dependence and dichotomized the subjects by positive or negative responses, we found that Gpp(NH)p- and forskolin-stimulated platelet AC activities were significantly lower among those alcohol-dependent subjects who had positive responses to questions related to drinking despite negative effects on mood ("Did you ever continue to drink even though you knew it was making you feel depressed, uninterested in things, or suspicious or distrustful of other people?"), drinking despite negative effects on health ("Did you ever continue to drink even though you knew it was causing you a health problem or making a health problem worse?"), or violence when drinking ("Did you get into physical fights while drinking or right after drinking?"). The alcohol-dependent subjects who had negative responses to these questions exhibited Gpp(NH)p- and forskolin-stimulated platelet AC activity that did not differ significantly from values in control subjects. The DSM-IV diagnosis of antisocial personality disorder did not distinguish alcohol-dependent subjects with regard to platelet AC activity. Gpp(NH)p and forskolin-stimulated AC activity may distinguish certain subtypes of alcoholics (i.e., those who develop negative mood in response to drinking, those who continue drinking despite health effects, and those who become violent while drinking).


Subject(s)
Adenylyl Cyclases/blood , Alcohol-Related Disorders/diagnosis , Alcoholism/diagnosis , Blood Platelets/enzymology , Adult , Alcohol-Related Disorders/enzymology , Alcohol-Related Disorders/genetics , Alcoholism/enzymology , Alcoholism/genetics , Antisocial Personality Disorder/diagnosis , Antisocial Personality Disorder/enzymology , Antisocial Personality Disorder/genetics , Comorbidity , Depressive Disorder, Major/diagnosis , Depressive Disorder, Major/enzymology , Depressive Disorder, Major/genetics , Female , Genetic Markers/genetics , Humans , Male , Middle Aged , Personality Inventory , Risk Factors
7.
Alcohol Clin Exp Res ; 22(9): 1955-61, 1998 Dec.
Article in English | MEDLINE | ID: mdl-9884138

ABSTRACT

Platelet adenylyl cyclase (AC) activity was measured in 32 alcohol-dependent subjects and 27 control subjects who were categorized as either family history-positive (FHP) or family history-negative (FHN) for alcoholism. The interview and blood sample collections were performed shortly after cessation of heavy drinking in the alcoholic group, and repeat blood samples were obtained at the end of the first and second weeks of monitored abstinence. Control subjects received the same interview and provided blood samples at the time of the interview. When subjects were not segregated for FHP or FHN status, there were no statistically significant differences in basal, cesium fluoride (CsF)-, or forskolin-stimulated mean AC activities between the controls and the alcoholics, at study entry or with 1 or 2 weeks of abstinence. On the other hand, over the 2-week course of sobriety from heavy drinking, the CsF-stimulated AC activity of FHP alcohol-dependent subjects decreased significantly (p = 0.03). FHP alcohol-dependent subjects after 2 weeks of sobriety had significantly lower mean CsF-stimulated AC activity than FHN controls (p = 0.04), whereas the FHN alcoholic subjects' CsF-stimulated AC activity did not differ significantly from FHN controls at this point in time. When all subjects were pooled and then categorized as either FHP or FHN, there was a significant difference in mean CsF-stimulated AC activity (p = 0.02) between the FHP and FHN subject groups. Genetic factors and abstinence appear to have roles in determining low platelet AC activity in alcoholic and nonalcoholic subjects. CsF-stimulated platelet AC activity, in particular, appears to act as a trait marker for a genetic vulnerability to developing alcoholism, but recent heavy drinking in male alcoholics is a factor that can mask differences between FHP and FHN subjects.


Subject(s)
Adenylyl Cyclases/genetics , Alcohol Withdrawal Delirium/genetics , Alcoholism/genetics , Blood Platelets/enzymology , Genetic Predisposition to Disease/genetics , Adenylyl Cyclases/blood , Adult , Alcohol Withdrawal Delirium/enzymology , Alcohol Withdrawal Delirium/rehabilitation , Alcoholism/enzymology , Alcoholism/rehabilitation , Enzyme Activation/genetics , Female , Genetic Markers/genetics , Humans , Male , Middle Aged , Sex Factors
8.
Cytogenet Cell Genet ; 83(3-4): 182-92, 1998.
Article in English | MEDLINE | ID: mdl-10072575

ABSTRACT

The Ursidae family includes eight species, the karyotype of which diverges somewhat, in both chromosome number and morphology, from that of other families in the order Carnivora. The combination of consensus molecular phylogeny and high-resolution trypsin G-banded karyotype analysis has suggested that ancestral chromosomal fissions and at least two fusion events are associated with the development of the different ursid species. Here, we revisit this hypothesis by hybridizing reciprocal chromosome painting probes derived from the giant panda (Ailuropoda melanoleuca), domestic cat (Felis catus), and man (Homo sapiens) to representative bear species karyotypes. Comparative analysis of the different chromosome segment homologies allowed reconstruction of the genomic composition of a putative ancestral bear karyotype based upon the recognition of 39 chromosome segments defined by painting as the smallest conserved evolutionary unit segments (pSCEUS) among these species. The different pSCEUS combinations occurring among modern bear species support and extend the postulated sequence of chromosomal rearrangements and provide a framework to propose patterns of genome reorganization among carnivores and other mammal radiations.


Subject(s)
Genome , Ursidae/genetics , Animals , Cats , Chromosome Painting , Chromosomes/genetics , DNA Probes , Evolution, Molecular , Humans , Karyotyping , Ursidae/classification
9.
Biol Psychiatry ; 42(1): 30-8, 1997 Jul 01.
Article in English | MEDLINE | ID: mdl-9193739

ABSTRACT

We investigated platelet adenylyl cyclase activity in 17 subjects with a history of major depression ("depressed subjects") and 20 controls. Forskolin was used to directly activate adenylyl cyclase, while guanine nucleotides (Gpp(NH)p) and fluoride ions were used to measure adenylyl cyclase activity modulated through the G proteins. Forskolin-stimulated adenylyl cyclase was significantly lower in the depressed subjects (p < 0.0005). There was a statistically significant difference in basal adenylyl cyclase activity between male depressed subjects and male controls. The basal adenylyl cyclase activity was also lower in female depressed subjects, but this difference did not reach statistical significance (p < 0.2). The adenylyl cyclase activity measured after stimulation with a guanine nucleotide or cesium fluoride did not differ between control and depressed male or female subjects. Severity of current depression and the current use of antidepressant medication were not related to the lower forskolin-stimulated enzyme activity in the depressed subjects. The difference in forskolin-stimulated adenylyl cyclase activity appears to reflect a qualitative difference in the adenylyl cyclase enzyme activity in persons with a history of major depression.


Subject(s)
Adenylyl Cyclases/blood , Blood Platelets/drug effects , Colforsin/pharmacology , Depressive Disorder/enzymology , Adult , Blood Platelets/enzymology , Enzyme Activation/drug effects , Female , Humans , Male , Middle Aged , Reference Values , Sex Factors
10.
Am J Med Genet ; 74(1): 95-8, 1997 Feb 21.
Article in English | MEDLINE | ID: mdl-9034014

ABSTRACT

Platelet adenylyl cyclase activity has been proposed as a trait marker for alcoholism [Tabakoff et al. (1988): N Engl J Med 318:134-13;9; Parsian et al. (1996): Alcohol Clin Exp Res 20:745-751]. Human adenylyl cyclase type 7 (ADCY7) is a member of the adenylyl cyclase gene family, and it may be the major form of adenylyl cyclase expressed in human platelets. The published cDNA sequence of ADCY7 indicated the presence of potentially polymorphic regions in the 3' untranslated region of ADCY7. PCR techniques combined with fluorescently labeled primers were used to amplify two separate tetranucleotide repeat regions [(AACA)n] in the 3' untranslated region of ADCY7 from the genomic DNA of 62 unrelated individuals. The upstream (AACA)4-repeat was not polymorphic. Five different genotypes were found in the downstream (AACA)5-7 tetranucleotide repeat region. We also tested the association of the tetranucleotide polymorphism to alcohol dependence. When 30 alcoholic and 17 control individuals were compared, no difference was found in the ADCY7 tetranucleotide polymorphism between alcohol-dependent and control groups. Nevertheless, to our knowledge these are the first polymorphisms reported in an adenylyl cyclase gene. Adenylyl cyclases are important receptor-G protein-coupled effectors and are involved in numerous neuronal functions in the central nervous system. Whether variations in ADCY7 and possible variations in other members of this gene family are underlying other psychiatric disorders remains to be studied.


Subject(s)
Adenylyl Cyclases/genetics , Alcoholism/genetics , Blood Platelets/enzymology , Microsatellite Repeats , Polymorphism, Genetic/genetics , Adenylyl Cyclases/chemistry , Alleles , Case-Control Studies , DNA Primers/chemistry , Fluorescent Dyes , Genotype , Humans , Molecular Sequence Data , Polymerase Chain Reaction
11.
Genomics ; 32(1): 1-14, 1996 Feb 15.
Article in English | MEDLINE | ID: mdl-8786094

ABSTRACT

The physical locations on human metaphase chromosomes of over 950 yeast artificial chromosome (YAC) clones from the CEPH library have been determined by fluorescence in situ hybridization and described as fractional chromosome length relative to the terminus of the short arm. Collectively, these clones contain approximately 1 billion basepairs of human DNA, about one-third of the human genome. In addition, the locations of 337 of these clones were established in terms of cytogenetic bands for chromosomes 1-18, 20, and X. Since most clones are positive for one or more of the Généthon polymorphic STS markers with defined genetic linkage distances corresponding to their physical locations, these data facilitate the integration of the cytogenetic, genetic, and physical maps of the human genome. Use of these mapping data in conjunction with public database information on CEPH YACs greatly facilitates the identification of YACs or polymorphic markers at specific locations in the genome.


Subject(s)
Chromosome Mapping , Genome, Human , Chromosome Banding , Chromosomes, Artificial, Yeast , Chromosomes, Human/genetics , Chromosomes, Human/ultrastructure , Cytogenetics , Databases, Factual , Female , Genetic Markers , Humans , In Situ Hybridization, Fluorescence , Male , Polymorphism, Genetic , Sequence Tagged Sites
12.
Proc Natl Acad Sci U S A ; 92(16): 7515-9, 1995 Aug 01.
Article in English | MEDLINE | ID: mdl-7638222

ABSTRACT

The DNA-activated serine/threonine protein kinase (DNA-PK) is composed of a large (approximately 460 kDa) catalytic polypeptide (DNA-PKcs) and Ku, a heterodimeric DNA-binding component (p70/p80) that targets DNA-PKcs to DNA. A 41-kbp segment of the DNA-PKcs gene was isolated, and a 7902-bp segment was sequenced. The sequence contains a polymorphic Pvu II restriction enzyme site, and comparing the sequence with that of the cDNA revealed the positions of nine exons. The DNA-PKcs gene was mapped to band q11 of chromosome 8 by in situ hybridization. This location is coincident with that of XRCC7, the gene that complements the DNA double-strand break repair and V(D)J recombination defects (where V is variable, D is diversity, and J is joining) of hamster V3 and murine severe combined immunodeficient (scid) cells.


Subject(s)
Chromosomes, Human, Pair 8 , DNA-Binding Proteins , Protein Serine-Threonine Kinases/genetics , Animals , Base Sequence , Binding Sites/genetics , Catalysis , Chromosome Banding , Chromosome Mapping , Chromosomes, Human, Pair 8/ultrastructure , Cricetinae , DNA Primers/genetics , DNA, Complementary/genetics , DNA-Activated Protein Kinase , Exons , Humans , In Situ Hybridization, Fluorescence , Introns , Mice , Molecular Sequence Data , Nuclear Proteins , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length , Protein Conformation , Protein Serine-Threonine Kinases/chemistry
13.
Insect Mol Biol ; 4(3): 161-7, 1995 Aug.
Article in English | MEDLINE | ID: mdl-8589842

ABSTRACT

Labelled recombinant cosmids were used as in situ hybridization probes to Aedes aegypti metaphase chromosomes. The cosmid probes yielded paired signals, one on each arm of sister chromatids, and they were ordered along the three chromosomes. In total, thirty-seven different probes were mapped to the three chromosomes of Ae. aegypti (2n = 6): twenty-eight to chromosome 1, six to chromosome 2, and six to chromosome 3. These results represent an initial stage in the generation of a physical map of the Ae. aegypti genome.


Subject(s)
Aedes/genetics , Genes, Insect , Animals , Cell Line , Chromosome Mapping , In Situ Hybridization, Fluorescence , Metaphase
14.
J Antimicrob Chemother ; 35(5): 593-601, 1995 May.
Article in English | MEDLINE | ID: mdl-7592172

ABSTRACT

Peptidyl-transfer RNA normally dissociates at a low rate from the ribosomes of Escherichia coli during protein synthesis but accumulates under nonpermissive conditions in cells with a temperature-sensitive allele (pthts) of the gene encoding peptidyl-transfer RNA hydrolase. The antibiotic-hypersensitive strain E. coli DB-11 with the pthts mutation was exposed to viomycin, then placed at nonpermissive temperatures. Under these conditions in the absence of drugs, peptidyl-tRNA accumulates, protein synthesis is inhibited and pthts cells die. When viomycin was present at sufficient concentration to arrest protein synthesis, cell death was not accelerated, error-inducing effects of streptomycin were not counteracted and, at high doses, cytoplasmic accumulation of peptidyl-transfer RNA was slowed down. Blocking the translocation of peptidyl-transfer RNA with viomycin did not stimulate its dissociation from ribosomes. Erythromycin-enhanced cell death was not affected by viomycin at doses sufficient to block amino acid incorporation, suggesting that short peptidyl-transfer RNAs could still be synthesized and dissociated from ribosomes.


Subject(s)
RNA, Transfer, Amino Acyl/drug effects , RNA, Transfer/drug effects , Viomycin/pharmacology , Drug Combinations , Erythromycin/pharmacology , Escherichia coli/drug effects , Escherichia coli/growth & development , Escherichia coli/metabolism , RNA, Transfer/biosynthesis , RNA, Transfer, Amino Acyl/biosynthesis
15.
Bull Am Acad Psychiatry Law ; 23(4): 523-32, 1995.
Article in English | MEDLINE | ID: mdl-8639980

ABSTRACT

This study was undertaken to investigate the authors' clinical impression that there are significant differences between the male and female insanity acquittees in Colorado, and that these differences result in significantly different treatment needs. The study sample included 149 patients: 112 men and 37 women committed to the Colorado Mental Health Institute at Pueblo as not guilty by reason of insanity (NGRI). Data were collected from a computerized data system and from chart reviews. The study provides descriptive data regarding demographic, legal, and mental health parameters of these acquittees. Demographic items included prior history of incarceration, age at first arrest, type of NGRI crime committed, and severity of NGRI crime. Mental health variables included prior psychiatric hospitalization history of suicide attempts, substance abuse history, inpatient substance abuse treatment history, diagnoses, escape history and length of stay. Percentages of male and female subjects were calculated for those variables with discrete categories. Means and medians were calculated for continuous variables. Results indicate that women are significantly more likely to be given a diagnosis of mood disorder or borderline personality disorder, are significantly older than men at the time of commitment, and are statistically more likely to have committed a single violent crime than men. Men were found to have a significantly higher rate of prior and current substance abuse, a significantly higher rate of antisocial personality disorder, a significantly greater history of violent crime prior to the NGRI offense, and arrests beginning at a significantly younger age than women. Despite the higher severity of crime rating for women, their length of stay was significantly shorter than for men. The implications of the findings with regard to different treatment needs are discussed, and the findings are compared to four other studies addressing female versus male insanity acquittees in other states.


Subject(s)
Commitment of Mentally Ill/legislation & jurisprudence , Expert Testimony/legislation & jurisprudence , Insanity Defense , Mental Disorders/diagnosis , Adult , Colorado , Crime/legislation & jurisprudence , Crime/psychology , Dangerous Behavior , Depressive Disorder/classification , Depressive Disorder/diagnosis , Depressive Disorder/rehabilitation , Female , Humans , Male , Mental Disorders/classification , Mental Disorders/rehabilitation , Personality Disorders/classification , Personality Disorders/diagnosis , Personality Disorders/rehabilitation , Sex Factors , Substance-Related Disorders/classification , Substance-Related Disorders/diagnosis , Substance-Related Disorders/rehabilitation , Violence/legislation & jurisprudence , Violence/psychology
16.
J Basic Clin Physiol Pharmacol ; 6(3-4): 229-50, 1995.
Article in English | MEDLINE | ID: mdl-8852269

ABSTRACT

During protein synthesis on the ribosome, the growing peptide is linked covalently to a transfer RNA. With a certain probability this peptidyl-tRNA dissociates from the ribosome, whereupon it becomes susceptible to hydrolysis catalyzed by peptidyl-tRNA hydrolase. When placed at nonpermissive temperatures, mutant (pthts) Escherichia coli that are temperature-sensitive for the hydrolase will accumulate peptidyl-tRNA, suffer inhibition of protein synthesis, and eventually die. Treating cells with chloramphenicol before raising the temperature prevents cell death but erythromycin, other macrolides, and lincosamide antibiotics all enhance cell death. Accumulation of peptidyl-tRNA by pthts cells at high temperatures is blocked by chloramphenicol but enhanced by macrolides and lincosamides. The data are most consistent with macrolide and lincosamide antibiotics having as their primary mechanism of inhibition the stimulation of peptidyl-tRNA dissociation from the ribosome. Rather than blocking peptide bond formation or peptidyl-tRNA translocation from the A- to the P-site of the ribosome, these antibiotics allow the synthesis of small peptides which dissociate as peptidyl-tRNAs before being completed. Low doses of erythromycin and lincomycin stimulate preferentially the dissociation of peptidyl-tRNAs that are erroneous. Errors in proteins can be assessed by the time necessary to inactivate beta-galactosidase at > 55 degrees C. Whether erroneous peptidyl-tRNAs are induced by treating E. coli with streptomycin or ethanol, or by starving for an amino acid, the shortened time to inactivate beta-galactosidase is counteracted if the cells are simultaneously treated with erythromycin or lincomycin. In contrast, errors in beta-galactosidase caused by synthesis in the presence of canavanine, an arginine analogue, cannot be counteracted by the simultaneous presence of erythromycin. This result rules out any effect of the drug on post-translational mechanisms of error correction.


Subject(s)
Anti-Bacterial Agents/metabolism , Escherichia coli/metabolism , Protein Synthesis Inhibitors/metabolism , RNA, Transfer, Leu/metabolism , Lincosamides , Macrolides/metabolism , Microbial Sensitivity Tests , Ribosomes/metabolism , Temperature , Time Factors , beta-Galactosidase/biosynthesis
17.
Mol Gen Genet ; 243(2): 225-33, 1994 Apr.
Article in English | MEDLINE | ID: mdl-8177219

ABSTRACT

Inaccurate protein synthesis produces unstable beta-galactosidase, whose activity is rapidly lost at high temperature. Erythromycin, lincomycin, clindamycin, and celesticetin were shown to counteract the error-inducing effects of streptomycin on beta-galactosidase synthesized in the antibiotic-hypersensitive Escherichia coli strain DB-11 Met-. Newly synthesized beta-galactosidase was more easily inactivated by high temperatures when synthesized by bacteria partially starved for arginine, threonine, or methionine. Simultaneous treatment with erythromycin or lincomycin yielded beta-galactosidase that was inactivated by high temperatures less easily than during starvation alone, an effect attributed to stimulation of ribosome editing. When synthesized in the presence of canavanine, beta-galactosidase was inactivated by high temperature more easily but this effect could not be reversed by erythromycin. The first arginine in beta-galactosidase occurs at residue 13, so the effect of erythromycin during arginine starvation is probably to stimulate dissociation of erroneous peptidyl-tRNAs of at least that length. Correction of errors induced by methionine starvation is probably due to stimulation of dissociation of erroneous peptidyl-tRNAs bearing peptides at least 92 residues in length. All the effects of erythromycin or the tested lincosamides on protein synthesis are probably the result of stimulating the dissociation from ribosomes of peptidyl-tRNAs that are erroneous or short.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacterial Proteins/biosynthesis , Protein Biosynthesis/drug effects , RNA, Transfer, Amino Acyl/metabolism , Ribosomes/metabolism , Arginine/metabolism , Carboxylic Ester Hydrolases/genetics , Carboxylic Ester Hydrolases/metabolism , Clindamycin/pharmacology , Culture Media , Erythromycin/pharmacology , Escherichia coli/drug effects , Escherichia coli/enzymology , Escherichia coli/genetics , Hot Temperature , Lincomycin/pharmacology , Methionine/metabolism , Mutation , Ribosomes/drug effects , Streptomycin/pharmacology , Threonine/metabolism , beta-Galactosidase/antagonists & inhibitors , beta-Galactosidase/biosynthesis
18.
Cytogenet Cell Genet ; 67(1): 61-7, 1994.
Article in English | MEDLINE | ID: mdl-8187555

ABSTRACT

Fluorescence in situ hybridization (FISH) provides a rapid approach to regional localization of overlapping clone sets (contigs) developed by various fingerprinting approaches. We have used 70 cosmid clones derived from 48 different contigs, part of the developing contig map of chromosome 16 (Stallings et al., 1990, 1992a), to cytogenetically map an estimated 8.6 million base pairs (Mbp) of chromosome 16 DNA (approximately 8-9% total coverage). Although the majority of cosmid contigs hybridized to single sites on chromosome 16, a significant fraction (23%) hybridized to multiple regions on chromosome 16; a subset of these also hybridized to other human chromosomes. In most instances, clones that mapped to multiple locations were found to contain low-abundance repetitive DNA sequences. The FISH data presented here, coupled with published mapping data from somatic cell hybrids (Callen et al., 1992), permits independent verification of the integrity of chromosome 16 cosmid contigs. The order of clones derived by FISH agrees closely with the cell hybrid mapping data and can be correlated with chromosome bands and specific chromosomal translocation breakpoints.


Subject(s)
Chromosomes, Human, Pair 16 , Repetitive Sequences, Nucleic Acid , Chromosome Mapping , Cosmids , Genetic Markers , Humans , In Situ Hybridization, Fluorescence
19.
Antimicrob Agents Chemother ; 37(9): 2027-9, 1993 Sep.
Article in English | MEDLINE | ID: mdl-8239627

ABSTRACT

At nonpermissive temperatures the peptidyl-tRNA hydrolase of pth(Ts) bacterial mutants is inactivated, and cells accumulate peptidyl-tRNA and die. Doses of erythromycin, lincomycin, or clindamycin that inhibited the growth of antibiotic-hypersensitive DB-11 pth+ cells accelerated the killing of DB-11 pth(Ts) cells at nonpermissive temperatures. Erythromycin and lincomycin also stimulated the accumulation of peptidyl-tRNA. Lincomycin and clindamycin stimulated peptidyl-tRNA dissociation from ribosomes.


Subject(s)
Anti-Bacterial Agents/pharmacology , Escherichia coli/drug effects , Macrolides , RNA, Transfer, Amino Acyl/metabolism , Ribosomes/metabolism , Carboxylic Ester Hydrolases/genetics , Carboxylic Ester Hydrolases/metabolism , Clindamycin/pharmacology , Erythromycin/pharmacology , Escherichia coli/enzymology , Escherichia coli/genetics , Lincomycin/pharmacology , Lincosamides , Mutation , RNA, Transfer, Amino Acyl/genetics , Ribosomes/drug effects , Temperature
20.
Genomics ; 16(1): 252-3, 1993 Apr.
Article in English | MEDLINE | ID: mdl-8486367

ABSTRACT

TFIIF (also termed FC) is a general transcription initiation factor that binds to RNA polymerase II and recruits it to a promoter. TFIIF is a heterodimer composed of 74-kDa (RAP74; gene symbol GTF2F1) and 30-kDa (RAP30; gene symbol GTF2F2) subunits. Here we report the mapping of the human GTF2F1 gene to band 19p13.3. Localization was performed by fluorescence in situ hybridization using the human RAP74 genomic cosmid clone as the probe.


Subject(s)
Chromosomes, Human, Pair 19 , Transcription Factors, TFII , Transcription Factors/genetics , Chromosome Banding , Chromosome Mapping , Cloning, Molecular , Cosmids , DNA Probes , Humans , In Situ Hybridization, Fluorescence
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