Abstract

We report on the presence of B-chromosomes in two populations of Dendropsophus nanus (= Hyla nana Boulenger, 1889) from Sao Paulo State, Brazil. Such chromosomes were observed in 4 out of 43 specimens (9.3%) and in 9 out of 15 specimens (60%) from the municipalities of Nova Alianca and Botucatu, respectively. The karyotype 2n = 30 + 1B found in D. nanus was similar to that of other species with 2n = 30 chromosomes, except for the presence of an additional small telocentric chromosome. In one specimen from Botucatu, cells with one to three extra chromosomes were observed. These B-chromosomes appeared as univalent in meiosis I and did not bear a nucleolar organizer region or exhibit constitutive heterochromatin.

Highlights

  • B-Chromosomes are extra chromosomes that occur in animals and plants and are generally considered dispensable for normal development, since they have no apparent function (Jones and Rees, 1982)

  • We describe the presence of B-chromosomes in specimens of Dendropsophus nanus (= Hyla nana Boulenger, 1889) from two populations collected at different sites in southeastern Brazil

  • The fluorescence in situ hybridization (FISH) probe consisted of a recombinant HM123 plasmid containing a fragment of Xenopus laevis rDNA (Meunier-Rotival et al, 1979), which was biotin-labelled by nick translation reaction using a BioNickTM Labeling System (Invitrogen)

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Summary

Introduction

B-Chromosomes are extra chromosomes that occur in animals and plants and are generally considered dispensable for normal development, since they have no apparent function (Jones and Rees, 1982). B-chromosomes bear no similarity to the autosomes, are inherited according to a non-Mendelian pattern, and occur as univalents in meiosis (Jones and Rees, 1982; Green, 1991, 2004). The number of B-chromosomes can vary among populations of the same species, among individuals in a population and among cells in an individual. In the latter case, this variation results from anaphase lag, with subsequent elimination of B-chromosomes from some cells or tissues, or, alternatively, it is caused by mitotic non-disjunction, with sister chromatids migrating to the same pole (Clark and Wall, 1996)

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