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Chromosome mapping of three common markers, ie major and 5S rRNA genes (rDNA) and telomeric repeats, and conventional chromosome bandings were applied to two sibling species, Apodemus sylvaticus Linnaeus, 1758 and A. flavicollis Melchior, 1834, to further investigate intra- and interspecific karyological differentiation in the genus Apodemus. A slight variation of the rDNA-patterns was detected between the two Apodemus species. In both of them, the major NORs were located on autosome pairs 8, 11, 12 and 22, while the two other rDNA sites detected on chromosomes 7 and 21 were variable in, respectively, A. sylvaticus and A. flavicollis. Several tiny rDNA sites were present on the sex chromosomes in both species, but their incidence was lower in A. flavicollis. Single 5S rDNA chromosomal sites were conserved on chromosome pair 20. No interstitial sites of telomeric repeats were present in either species. In the Sicilian population of A. sylvaticus, the constitutive heterochromatin pattern corresponded to the “sylvaticus-E1” cytotype, while A. flavicollis had a species-specific pattern restricted to centromeres of all chromosomes. The results are discussed in relation to cytogenetic data available for the genus, with emphasis on the Sylvaemus group/subgenus.
This paper presents a case study of the chromosomal complement of 16 mice Mus , musculus domesticus Linnaeus, r 1758 from the region near one of the most recent disastrous earthquakes in Italy (named Umbria-Marche 1997), with the aim of ex­amining chromosomal variability among the mice from the seismically active zones. For the present investigation, the sampling sites were chosen in the vicinity of some active faults, supposedly the main earthquake generators in the area. In the three localities, that lie approximately on the fault lines, mice with a reduced chromosomal number (2n = 36 to 39) were trapped. This reduction is due to the presence of three different Robertsonian metacentrics - Rb(9.14), Rb(10.12) and Rb(15.17) - in both the homo­zygous and heterozygous states. Mice trapped in four localities more distant from the fault zone only had the standard karyotype (2n = 40). These results increase the need to analyze in more detail the distribution of karyotypes in relation with active faults.
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