An Effect of Centromere Function on the Behavior of Ring-X Chromosomes in DROSOPHILA MELANOGASTER

It is shown that under the influence of an autosomal meiotic mutant that causes abnormalities in meiotic centromere function (mei-S332), ring-X chromosomes are frequently nonrecoverable. Evidence is presented that this nonrecoverability is caused by a failure of sister ring-chromatids to successfully effect an equational separation with resultant dominant lethality. Because mei-S332 results in meiotic abnormalities only after replication has been completed, and because ring chromosomes are normally transmitted with approximately the same efficiency as rod chromosomes, it is suggested that during replication in normal meioses, sister ring-chromatids form mutually interlocked ring complexes that are resolved without genetic consequences at anaphase II, with the resolution owing at least in part to normal centromere function.     

The Birth of the Centromere

The centromere is the region of the eukaryotic chromosome that determines kinetochore formation and sister chromatid cohesion. Centromeres interact with spindle microtubules to ensure chromatid segregation during mitosis and homologous chromosome segregation during meiosis I. In recent years, the overall organization of centromeres in several eukaryotic species has been described, yet the mechanisms of centromere definition remain elusive. Understanding the evolutionary origin of the centromere may well elucidate aspects of its function. With such intention, we hypothesize that centromeres were derived from telomeres during the evolution of the eukaryotic chromosome. We propose that the proto-eukaryotic cell could not have evolved a nucleus without concurrently evolving a new tubulin-based cytoskeleton, the microtubules, and a specific chromosomal region that enabled the chromosome-microtubule interaction, the centromere. The repetitive nature of the subtelomeric regions that gave rise to the centromeres forced the concerted evolution of the centromeres. Although this implies the absence of a conserved primary sequence, a conserved centromere-specific structural motif could still exist and determine where in the chromosome the centromere is to be formed.To support the “centromeres-from-telomeres” hypothesis, we discuss several situations, in meiosis and mitosis, where telomeric regions took over centromeric roles. The recently discovered phenomenon of centromere repositioning is also discussed because it has revealed new insights into how neocentromeres evolve.     

Geitler's Nucleolar Substance in Spirogyra

The movements of Geitler's ‘nucleolar substance’,a deeply staining material found in the mitotic nucleus afterbreakdown of the nucleolus, are traced in fifteen species ofSpirogyra including two of those originally used. Deposition of nucleolar substance on metaphase and anaphasechromosomes, noted by Geitler, is confirmed. Observed for thefirst time are the sloughing-off from the anaphase chromatidsof nucleolar substance and its distribution in and by the spindle,independent of the chromosomes.     

Centromere repositioning in mammals

The evolutionary history of chromosomes can be tracked by the comparative hybridization of large panels of bacterial artificial chromosome clones. This approach has disclosed an unprecedented phenomenon: 'centromere repositioning', that is, the movement of the centromere along the chromosome without marker order variation. The occurrence of evolutionary new centromeres (ENCs) is relatively frequent. In macaque, for instance, 9 out of 20 autosomal centromeres are evolutionarily new; in donkey at least 5 such neocentromeres originated after divergence from the zebra, in less than 1 million years. Recently, orangutan chromosome 9, considered to be heterozygous for a complex rearrangement, was discovered to be an ENC. In humans, in addition to neocentromeres that arise in acentric fragments and result in clinical phenotypes, 8 centromere-repositioning events have been reported. These 'real-time' repositioned centromere-seeding events provide clues to ENC birth and progression. In the present paper, we provide a review of the centromere repositioning. We add new data on the population genetics of the ENC of the orangutan, and describe for the first time an ENC on the X chromosome of squirrel monkeys. Next-generation sequencing technologies have started an unprecedented, flourishing period of rapid whole-genome sequencing. In this context, it is worth noting that these technologies, uncoupled from cytogenetics, would miss all the biological data on evolutionary centromere repositioning. Therefore, we can anticipate that classical and molecular cytogenetics will continue to have a crucial role in the identification of centromere movements. Indeed, all ENCs and human neocentromeres were found following classical and molecular cytogenetic investigations.     

Centromere Epigenetics in Plants

The centromere is an essential chromosome site at which the kinetochore forms and loads proteins needed for faithful segregation during the cell cycle and meiosis(Houben et al., 1999;Cleveland et al.,2003;Ma et al.,2007;Birchler and Han,2009).Centromere specific sequences such as tandem repeats or transposable elements evolve quickly both within and between the species but have conserved kinetochore proteins(Henikoff and Furuyama,2010).The universal feature     

Cytological Identification of the Chromosomes Involved in Searle''s Translocation and the Location of the Centromere in the X Chromosome of the Mouse

The autosome in Searle's X-autosome translocation has been shown to be chromosome 16. The breakpoint in chromosome 16 is slightly proximal to the middle and in the X is slightly distal to the middle.-Available evidence indicates that either Linkage Group XV or Linkage Group XIX is carried on chromosome 16.-The centromere of the X chromosome is at the spf end of the linkage group.     

Centromere staining at meiosis in man

Summary A recently-developed barium hydroxide/saline/giemsa technique has been used to demonstrate constitutive heterochromatin in human male meiotic chromosomes. The technique aids bivalent identification at diakinesis and has been applied to an analysis of meiosis in two patients with normal karyotypes and two translocation heterozygotes.

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Zusammenfassung Mit Hilfe der kürzlich entwickelten Bariumhydroxyd/Kochsalz/Giemsa-Technik wurde konstitutives Heterochromatin an männlichen Meiosechromosomen des Menschen gefärbt. Die Methode ermöglicht die Identifizierung der bivalents in der Diakinese. Sie wurde zur Meiose-Analyse verwendet bei 2 Patienten mit normalem Karyotyp und 2 Translokations-Heterozygoten.

     

Centromere mitotic recombination in mammalian cells

Centromeres are special structures of eukaryotic chromosomes that hold sister chromatid together and ensure proper chromosome segregation during cell division. Centromeres consist of repeated sequences, which have hindered the study of centromere mitotic recombination and its consequences for centromeric function. We use a chromosome orientation fluorescence in situ hybridization technique to visualize and quantify recombination events at mouse centromeres. We show that centromere mitotic recombination occurs in normal cells to a higher frequency than telomere recombination and to a much higher frequency than chromosome-arm recombination. Furthermore, we show that centromere mitotic recombination is increased in cells lacking the Dnmt3a and Dnmt3b DNA methyltransferases, suggesting that the epigenetic state of centromeric heterochromatin controls recombination events at these regions. Increased centromere recombination in Dnmt3a,3b-deficient cells is accompanied by changes in the length of centromere repeats, suggesting that prevention of illicit centromere recombination is important to maintain centromere integrity in the mouse.     

Inhibition of Etiolation in Spirogyra by Phytochrome

Cells of Spirogyra filaments grown in darkness become longer than light grown cells. This elongation can be prevented by a few minutes of red light given with intervals of 24 h under the dark period. Far-red light given after the red light pulse counteracts the red light effect. Cells which have finished their elongation in light do not elongate further in darkness. Along with the cell elongation the chloroplasts become less spirally wound and ultimately shortened to straight bands.     

A Simple Method for Rapid Detection of Chromosomes or Nuclei in Yolk-Rich Avian Oocytes or Eggs

As early as 1914 Van Durme described how difficult it is to detect the small avian chromosomes among the enormous mass of yolk granules at the end of oogenesis. During the ensuing fertilization and early cleavage period, he could hardly follow the rapidly changing morphology of the nuclei and chromosomes, since the classical staining methods also stained the intervitelline material.     

The seasonal dynamics of Spirogyra in a shallow,maritime Antarctic lake

Summary The filamentous chlorophyte Spirogyra forms a mat covering extensive areas of Spirogyra Lake, a small, shallow, Antarctic lake. It has an annual growth pattern, with a maximum standing crop of 400 g chlorophyll- m^-2 during the ice-free summer period. Nutrient concentrations were low and there was evidence for P-limitation. The attainment of such a high standing crop was probably dependent on the lake's high specific dilution rate. Radiation flux was very low under winter ice cover and Spirogyra died back almost completely. The lake water became hypoxic and inorganic nutrients accumulated in both the water column and overwintering algal filaments. Spore formation was not observed, but changes in the composition of filaments indicated that polysaccharides, which had accumulated in summer, were depleted over the long, ice-covered winter period.     

Widespread Gene Conversion in Centromere Cores

Centromeres are the most dynamic regions of the genome, yet they are typified by little or no crossing over, making it difficult to explain the origin of this diversity. To address this question, we developed a novel CENH3 ChIP display method that maps kinetochore footprints over transposon-rich areas of centromere cores. A high level of polymorphism made it possible to map a total of 238 within-centromere markers using maize recombinant inbred lines. Over half of the markers were shown to interact directly with kinetochores (CENH3) by chromatin immunoprecipitation. Although classical crossing over is fully suppressed across CENH3 domains, two gene conversion events (i.e., non-crossover marker exchanges) were identified in a mapping population. A population genetic analysis of 53 diverse inbreds suggests that historical gene conversion is widespread in maize centromeres, occurring at a rate >1×10⁻⁵/marker/generation. We conclude that gene conversion accelerates centromere evolution by facilitating sequence exchange among chromosomes.