Triosephosphate isomerase: a highly evolved biocatalyst

Triosephosphate isomerase (TIM) is a perfectly evolved enzyme which very fast interconverts dihydroxyacetone phosphate and d-glyceraldehyde-3-phosphate. Its catalytic site is at the dimer interface, but the four catalytic residues, Asn11, Lys13, His95 and Glu167, are from the same subunit. Glu167 is the catalytic base. An important feature of the TIM active site is the concerted closure of loop-6 and loop-7 on ligand binding, shielding the catalytic site from bulk solvent. The buried active site stabilises the enediolate intermediate. The catalytic residue Glu167 is at the beginning of loop-6. On closure of loop-6, the Glu167 carboxylate moiety moves approximately 2 Å to the substrate. The dynamic properties of the Glu167 side chain in the enzyme substrate complex are a key feature of the proton shuttling mechanism. Two proton shuttling mechanisms, the classical and the criss-cross mechanism, are responsible for the interconversion of the substrates of this enolising enzyme.     

Fluorescence replication banding of frog chromosomes

To identify individual chromosomes of a frog karyotype by their fluorescence banding patterns, chromosomes were stained with actinomycin D and 4,6-diamidino-2-phenylindole (DAPI) after incorporation of BrdU during the late S-phase. The chromosomes of three Rana species which were selected for this study (R. ridibunda, R. lessonae and R. japonica) showed well-defined late replication bands. The fluorescence patterns obtained were the reverse of those produced by a 4Na-EDTA Giemsa-staining technique. Fluorescence patterns of the two water frog species (R. ridibunda and R. lessonae) were similar to each other, except for the different fluorescence of the centromeric heterochromatin, which gave extremely bright signals in R. ridibunda but no signal in R. lessonae. Experiments also showed differences between the fluorescence patterns of R. lessonae chromosome 13 in the Italian and Luxembourgian populations. These results sho w that the fluorescence replication banding using actinomycin D and DAPI is very effective in identifying individual frog chromosomes and detecting their structural changes. Received 7 June 1996; received after revision 23 July 1996; accepted 21 August 1996     

The karyotype ofMicrotus cabrerae Thomas,another species with giant sex chromosomes

Summary The karyotype ofMicrotus cabrerae, a species endemic to Spain, is described. It comprises 2n=54 chromosomes, with a fundamental number of 64, and with very large sex chromosomes. An evolutionary relationship between this species andM. chrotorrhinus is suggested.     

Second discovery of multiple sex chromosomes among fishes

Zusammenfassung Bei einer bisher nicht beschriebenen mexikanischen Fischart werden 41 Autosomen beim Männchen und 42 beim Weibchen gefunden. Die Befunde sprechen für ein System multipler Sexualchromosomen dieser Fische.     

Late DNA replication in the sex chromosomes ofDidelphis virginiana

Zusammenfassung Autoradiographisch wurde die späte DNS-Synthese derX- undY-Chromosomen vonDidelphis virginiana (Virginia Opossum) in Knochenmarkzellen untersucht. Die weiblichen Tiere zeigen typische späte Reduplikationsmuster in einemX, die männlichen das späte Reduplikationsmuster inX undY und inY allein.

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This study was supported in part by research grant No. AM-02504 and training grant No. Tl-AM-5277, National Institutes of Health. Dr.Reiss was a predoctoral trainee, National Institute of Arthritis and Metabolic Diseases, U.S. Public Health Service.     

G-banding patterns of the housefly,Musca domestica,autosomes and sex chromosomes

Summary G-banding patterns were found on the X-chromosomes of the housefly. This indicates the presence of major gene loci on these chromosomes, i.e. sex-linked genes. G-banding patterns were also found on the Y-chromosome of 2 preparations. The first polyploid cell (a tetraploid, 2n=24) forMusca domestica was observed in one of the banding preparations.     

RNA synthesis in the sex chromosomes of the opossum,Didelphis virginiana. I. Female

Résumé Pour une étude quantitative de la synthèse du RNA, nous avons utilisé des chromosomes sexuels d'Opossum, morphologiquement faciles à distinguer en prophase et possédant des caractères cytogénétiques inusuels. Les résultats suggèrent que les deux chromosomesX des lymphocytes femelles sont actifs génétiquement (quoique l'un d'eux le soit moins que l'autre) pendant une courte période du cycle de la cellule.     

Appearance of sex hormone receptors in frog (Rana esculenta) tadpole skin during metamorphosis.

In tadpole skin of Rana esculenta, a specific testosterone receptor was detected during the climax in both males and females. The Kass ranged between 1 and 2.79 x 10(9)M-1.     

Differential reaction of tomato chromosomes with hydroxylamine

Zusammenfassung Hydroxylamin, welches spezifisch mit Cytosin reagiert, stört die Struktur der verschiedenen Chromosomen in Pollenmutterzellen der Tomate unterschiedlich stark. Das Chromosomenpaar Nr. 2 wird wesentlich weniger stark geschädigt als die übrigen. Die Bedeutung dieses Befundes wird kurz angedeutet.