To study whether specific DNA sequences are associated with nuclear membranes, residual DNA was extracted from DNase-treated nuclear envelopes prepared from erythrocytes of adult chickens (Gallus domesticus). This DNA was then blunt-end ligated into a bacterial plasmid vector. DNA blot analysis and nucleotide sequence determination revealed that approximately 30% of the cloned fragments consisted of different multiples of a 41-42 bp tandemly repeated, partially symmetrical sequence. In situ hybridization to chicken chromosomes demonstrated that the sequence was located primarily on microchromosomes, although some hybridization was also observed to macrochromosomes 7 and 8. Digestion of chicken DNA with any of a number of restriction enzymes did not completely reduce the intensity of a high molecular weight band to which the repeated sequence hybridized. These results, along with those obtained from in situ hybridization, suggested that many copies of this sequence are organized into large tandem arrays, and are not dispersed in many shorter repetitive blocks throughout the chicken genome. Although the repetitive sequence constituted approximately 10% of the chicken genome, it did not hybridize to quail or turkey DNA.

Whole-cell protein patterns of a psychrotrophic Bacillus cereus strain from cultures grown at 7 and 30؇C were compared. This analysis revealed that at least three major proteins are expressed at a significantly higher rate at 7؇C than at 30؇C. The most abundant of these cold-induced proteins was a small polypeptide of 7.5 kDa, designated CspA, of B. cereus. In addition, four small proteins very similar in size to CspA were seen on both 7؇C and 30؇C two-dimensional protein gels. Immunoblot analysis using B. cereus anti-CspA antibodies indicated that the five proteins described above plus an additional sixth protein not visible on silver-stained two-dimensional gels are members of a B. cereus cold shock protein family. This hypothesis was corroborated by cloning and sequencing of the genes encoding five proteins of this family. The protein sequences deduced are highly similar and show homology to small procaryotic cold shock proteins and to the cold shock domain of eucaryotic Y-box proteins. Besides CspA, only one of the additional five CspA homologs was slightly cold inducible. In the presence of 100 mM NaCl, the two purified members of the protein family (CspA and CspE) elute as dimers at an apparent molecular mass of 15 kDa from a gel filtration column. At higher salt concentrations, they dissociate into their monomers. Their ability to bind to the ATTGG motif of singlestranded oligonucleotides was demonstrated by band shift analysis.

We present a general model for the evolution of chromosome-specific satellite DNA subfamilies. Sus scrofa domestica has a bimodal karyotype with two autosomal subsets of 12 meta-/submetacentric (Mc) and 6 acrocentric (Ac) chromosome types (Mc and Ac "subgenomes"). We show that the centromeric heterochromatin is characterised by two distinct satellite DNA families designed Mc1 and Ac2. Mc1 is a diverse satellite family of the Mc subgenome of which certain members with a 100 bp repeat unit are found to occur at the pericentromeric regions of each Mc autosome, while others are chromosome-specific, e.g. clone Mc pAv1.5, a higher order repeat variant, which hybridises specifically to chromosome 1. Ac2 is a homogeneous satellite occurring at the subterminal pericentromeric regions of all Ac autosomes. DNA sequence analyses showed that all clones investigated are built up from a 14 bp repeat unit which is highly conserved. In situ hybridisation to meiotic pachytene nuclei revealed a distinct spatial arrangement of the Ac2 centromeric satellite.

Chicken chromosomes were identified up to No. 18 by a sequential counterstain-enhanced fluorescence technique. A heterochromatin characterization of macro- and microchromosomes was performed; in general, the microchromosomes were GC-rich, but with a high degree of variation. The NORs are localized on chromosome No. 17.

The karyotype of the perch (Percafluviatilis L.) was analysed by means of silver-staining, the chromomycin A3/Distamycin A/DAPI and Actinomycin D fluorescence technique in order to locate active NORs and to selectively highlight certain heterochromatic regions. The ribosomal RNA genes are localized at the secondary constrictions of the short arms of chromosomes no. 16. Additionally, bright chromomycin fluorescence was observed in the same regions. No DAPI/Distamycin A bright heterochromatic block was detected in the perch karyotype. I:~,. I. Sequential Ag-CDD-DAPI Actinomycin D staining of a lymphocyte metaphase of a male perch: (a) Ag-NOR-staining, note two Ag-NORs on two chromosomes no. 16: (bJChromomycinstaining. note brilliant chromomycin fluorescence associated with NOR regions: {c) DAPI Distamycin A. notelack of differentially stained fluorescence block,: Id) DAPl'Actinomycin Dstaining.