C-band differentiation between the chromosomes of two subspecies of the chironomid midgeChironomus thummi

Summary The metaphase chromosomes ofChironomus th. thummi contain approximately 17% more pericentric C-band heterochromatin than the chromosomes ofChironomus th. piger with 11% heterochromatin. InCh. th. thummi, the proportion of heterochromatin appeared to be much larger in metaphase chromosomes than in polytene chromosomes. This discrepancy is interpreted as being due to the specific chromosome organization and not as the result of an underreplication of heterochromatin during polytenization.     

SET domain proteins modulate chromatin domains in eu- and heterochromatin

The SET domain is a 130-amino acid, evolutionarily conserved sequence motif present in chromosomal proteins that function in modulating gene activities from yeast to mammals. Initially identified as members of the Polycomb- and trithorax-group (Pc-G and trx-G) gene families, which are required to maintain expression boundaries of homeotic selector (HOM-C) genes, SET domain proteins are also involved in position-effect-variegation (PEV), telomeric and centromeric gene silencing, and possibly in determining chromosome architecture. These observations implicate SET domain proteins as multifunctional chromatin regulators with activities in both eu- and heterochromatin – a role consistent with their modular structure, which combines the SET domain with additional sequence motifs of either a cysteine-rich region/zinc-finger type or the chromo domain. Multiple functions for chromatin regulators are not restricted to the SET protein family, since many trx-G (but only very few Pc-G) genes are also modifiers of PEV. Together, these data establish a model in which the modulation of chromatin domains is mechanistically linked with the regulation of key developmental loci (e.g. HOM-C).     

Distribution of sister chromatid exchanges in different types of chromatin in the X chromosome ofMicrotus cabrerae

We used the X chromosomes ofMicrotus cabrerae as a model to analyze the distribution of sister chromatid exchanges (SCEs) on different types of chromatin, because of the marked heterogeneity of the heterochromatin in the entire short arm and a portion of the long arm of this chromosome. Computer-simulated distributions, according to an algorithm that makes it possible to modify the distribution on the basis of any possible hypothesis, were compared with real distributions by log-linear models. We found that the frequency of SCEs in different types of heterochromatin was higher than that expected for a random distribution, and located an SCE hot-spot at the junction between euchromatin and heterochromatin. The possible relationship between the distribution of SCEs and base composition or chromatin accessibility are discussed.     

Chromosomal variation and heterochromatin polymorphisms inPeromyscus maniculatus

Summary Evidence is presented that chromosomal variation inPeromyscus results from 1. addition of heterochromatic short arms to acrocentric chromosomes, and 2. pericentric inversions. Constitutive heterochromatin polymorphisms contribute to variation in the amount of heterochromatin inPeromyscus populations.Submitted in partial fulfilment of the requirements of Master of Science degree in Zoology at the University of Wyoming.Supported in part by Public Health Service Grant No. GM-20491 from the National Institute of Health and by grants from the U. Wyoming Division of Basic Research and Research Coordination.     

Heterochromatin characterization and distribution in the chromosomes of two populations ofIdotea baltica basteri Audouin, 1826 (Isopoda,Valvifera)

Two mediterranean populations ofIdotea baltica basteri from Messina and Naples showed a set of chromosomes composed by 58 all-biarmed chromosomes. The heterochromatin was located in the pericentromeric region of the chromosomes, and its composition appeared heterogeneous. In fact, not all the homologs showed heterochromatin resistant to digestion with three restriction enzymes (Alu I, Hae III and Sau 3A). Moreover, the two populations showed polymorphism in a band of G+C-rich telomeric heterochromatin, which was present only in the population from Messina. It is hypothesized that chromosomal polymorphism might reflect the geographical isolation of the two populations. It is also suggested that a process of diversification is taking place.     

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     

Distribution of constitutive heterochromatin (C-bands) in the somatic chromosomes of an Indian bird,Chrysomma sinense (Gmelin)

Summary The localization of constitutive heterochromatin has been studied in a passerine bird,Chrysomma sinense (2n=±70). In all the 7 pairs of macrochromosomes pericentric heterochromatin has been observed as usual except in pairs Nos 2 and 4, in which both pericentric and non-centromeric heterochromatin have been recorded.The authors are grateful to Prof. B. K. Behura, Department of Zoology, Utkal University, for necessary laboratory and library facilities. T.S. is grateful to the CSIR for providing financial assistance under the JRF scheme.     

The karyotype,C-bands and AgNO3-bands of a lungless salamander from Korea:Onychodactylus fischeri (Boulenger) (Amphibia,Urodela)

The karyotype of a lungless salamander,Onychodactylus fischeri, from Korea was analyzed and compared with that of the Japanese congeneric species,O. japonicus. In both species the diploid karyotype consists of78 chromosomes, including 6 pairs of large chromosomes, 6 pairs of medium-sized ones, and the remaining 27 pairs of microchromosomes. The chromosome number ofO. fischeri, 2n=78, is, like that ofO. japonicus, the largest so far reported in the order Urodela. C-banding showed that constitutive heterochromatin inO. fischeri was mainly in the centromeric regions and near the secondary constrictions of the large chromosomes. AgNO₃-bands were located in the secondary constrictions associated with C-band heterochromatin.     

Centromeric heterochromatin in the karyotype of the male Greater Kudu (Tragelaphus strepsiceros)

Summary The chromosomes of a male Kudu (Tragelaphus strepsiceros) have been studied by C-banding and H³ thymidine labelling. It is suggested that heterochromatin may have accumulated on the 14th pair of autosomes before its translocation to the Y-chromosome.     

Unusual distribution of constitutive heterochromatin (C-bands) in the somatic chromosomes of a passerine birdErithacus svecicus

Summary The distribution of constitutive heterochromatin (C-bands) has been studied in a passerine bird,Erithacus svecicus (Linnaeus) (Turdidae, Passeriformes, Aves) (2n=76±). In 7 out of 9 pairs of macrochromosomes pericentromeric heterochromatin has been observed. The smaller 2 pairs of macrochromosomes are entirely heterochromatic.The authors are grateful to Prof. B.K. Behura, P.G. Dept. of Zoology, Utkal University for extending laboratory and library facilities. T.S. is grateful to CSIR, India for providing financial assistance under SRF scheme.     

Chromosome boundary elements and regulation of heterochromatin spreading

Chromatin is generally classified as euchromatin or heterochromatin, each with distinct histone modifications, compaction levels, and gene expression patterns. Although the proper formation of heterochromatin is essential for maintaining genome integrity and regulating gene expression, heterochromatin can also spread into neighboring regions in a sequence-independent manner, leading to the inactivation of genes. Because the distance of heterochromatin spreading is stochastic, the formation of boundaries, which block the spreading of heterochromatin, is critical for maintaining stable gene expression patterns. Here we review the current understanding of the mechanisms underlying heterochromatin spreading and boundary formation.