Hybrid ape offspring of a mating of gibbon and siamang

Science ◽  
1979 ◽  
Vol 205 (4403) ◽  
pp. 308-310 ◽  
Author(s):  
RH Myers ◽  
DA Shafer

The serendipitous mating of a male gibbon, Hylobates moloch, and a female siamang, Symphalangus syndactylus, has produced two female offspring born 1 year apart. The hybrid karyotype of 47 chromosomes comprises the haploid complements of the parental species, 22 for the gibbon and 25 for the siamang. Chromosomal G and C banding comparisons revealed no clear homologies between the parental karyotypes except for the single chromosome in each species containing the nucleolus organizer region. The lack of homology suggests that the structural rearrangement of chromosomes has played a major role in the process of speciation for these lesser apes.

2016 ◽  
Vol 14 (2) ◽  
Author(s):  
Larissa A. Medeiros ◽  
Eduardo G. Ginani ◽  
Leandro M. Sousa ◽  
Lúcia H. Rapp Py-Daniel ◽  
Eliana Feldberg

ABSTRACT Baryancistrus xanthellus is a species from the Ancistrini tribe known commonly as "amarelinho " or "golden nugget pleco". It is one of the most popular and valued ornamental fishes due to its color pattern. Also, it is an endemic species from the Xingu River occurring from Volta Grande do Xingu, region where the Belo Monte Hydropower Dam is being built, to São Félix do Xingu. The current study aimed to cytogenetically characterize B. xanthellus . Results point to the maintenance of 2n=52, which is considered the most common condition for the tribe, and a single nucleolus organizer region (NOR). Mapping of the 18S rDNA confirmed the NOR sites, and the 5S rDNA was mapped in the interstitial position of a single chromosome pair. The 18S and 5S rDNA located in different pairs constitute an apomorphy in Loricariidae. Large blocks of heterochromatin are present in pairs 1 and 10 and in the regions equivalent to NOR and the 5S rDNA. Data obtained in this study corroborated with the currently accepted phylogenetic hypothesis for the Ancistrini and demonstrate evidence that the genus Baryancistrus occupies a basal position in the tribe.


Animals ◽  
2021 ◽  
Vol 11 (9) ◽  
pp. 2551
Author(s):  
Agnese Petraccioli ◽  
Paolo Crovato ◽  
Fabio Guarino ◽  
Marcello Mezzasalma ◽  
Gaetano Odierna ◽  
...  

We performed a molecular and a comparative cytogenetic analysis on different Helicoidea species and a review of all the available chromosome data on the superfamily to provide an updated assessment of its karyological diversity. Standard karyotyping, banding techniques, and Fluorescence in situ hybridization of Nucleolus Organizer Region loci (NOR-FISH) were performed on fifteen species of three families: two Geomitridae, four Hygromiidae and nine Helicidae. The karyotypes of the studied species varied from 2n = 44 to 2n = 60, highlighting a high karyological diversity. NORs were on a single chromosome pair in Cernuella virgata and on multiple pairs in four Helicidae, representing ancestral and derived conditions, respectively. Heterochromatic C-bands were found on pericentromeric regions of few chromosomes, being Q- and 4′,6-diamidino-2-phenylindole (DAPI) negative. NOR-associated heterochromatin was C-banding and chromomycin A3 (CMA3) positive. Considering the available karyological evidence on Helicoidea and superimposing the chromosome data gathered from different sources on available phylogenetic inferences, we describe a karyotype of 2n = 60 with all biarmed elements as the ancestral state in the superfamily. From this condition, an accumulation of chromosome translocations led to karyotypes with a lower chromosome number (2n = 50–44). This process occurred independently in different lineages, while an augment of the chromosome number was detectable in Polygyridae. Chromosome inversions were also relevant chromosome rearrangements in Helicoidea, leading to the formation of telocentric elements in karyotypes with a relatively low chromosome count.


1996 ◽  
Vol 250 (1) ◽  
pp. 123-128
Author(s):  
Georg Haberer ◽  
Thilo C. Fischer ◽  
Ramón A. Torres-Ruiz

1988 ◽  
Vol 51 (2) ◽  
pp. 103-109 ◽  
Author(s):  
Jennifer A. Marshall Graves ◽  
Garey W. Dawson

SummaryIn marsupials, X chromosome inactivation is paternal and incomplete. The tissue-specific pattern of inactivation of X-linked loci (G6PD, PGK, GLA) has been attributed to a piecemeal inactivation of different regions of the X. We here propose an alternative hypothesis, in which inactivation of the marsupial X is a chromosome-wide event, but is differentially regulated in different tissues. This hypothesis was suggested by the relationship between the positions and activity of genes on the kangaroo paternal X. In the absence of an HPRT polymorphism, we have used somatic cell hybridization to assess the activity of the paternal HPRT allele in lymphocytes and fibroblasts. The absence of the paternal X, and of the paternal forms of G6PD or PGK, from 33 cell hybrids made by fusing HPRT-deficient rodent cells with lymphocytes or fibroblasts of heterozygous females, suggests that the HPRT gene on the paternal X is inactive in both tissues and therefore not selectable. Since HPRT is located medially on the Xq near GLA, which shares the same characteristics of activity, we suggest that the locus-specific and tissue-specific patterns of activity result from a differential spread of inactivation from a single control locus, located near HPRT and GLA, outwards in both directions to G6PD and PGK. The nucleolus organizer region on the short arm does not seem to be part of the inactivated unit.


2007 ◽  
Vol 18 (2) ◽  
pp. 369-379 ◽  
Author(s):  
Frederic Pontvianne ◽  
Isabel Matía ◽  
Julien Douet ◽  
Sylvette Tourmente ◽  
Francisco J. Medina ◽  
...  

Nucleolin is one of the most abundant protein in the nucleolus and is a multifunctional protein involved in different steps of ribosome biogenesis. In contrast to animals and yeast, the genome of the model plant Arabidopsis thaliana encodes two nucleolin-like proteins, AtNUC-L1 and AtNUC-L2. However, only the AtNUC-L1 gene is ubiquitously expressed in normal growth conditions. Disruption of this AtNUC-L1 gene leads to severe plant growth and development defects. AtNUC-L1 is localized in the nucleolus, mainly in the dense fibrillar component. Absence of this protein in Atnuc-L1 plants induces nucleolar disorganization, nucleolus organizer region decondensation, and affects the accumulation levels of pre-rRNA precursors. Remarkably, in Atnuc-L1 plants the AtNUC-L2 gene is activated, suggesting that AtNUC-L2 might rescue, at least partially, the loss of AtNUC-L1. This work is the first description of a higher eukaryotic organism with a disrupted nucleolin-like gene and defines a new role for nucleolin in nucleolus structure and rDNA chromatin organization.


1985 ◽  
Vol 27 (5) ◽  
pp. 491-497 ◽  
Author(s):  
J. P. M. Camacho ◽  
J. Belda ◽  
J. Cabrero

While silver impregnation reveals the presence of kinetochores in monocentric chromosomes, it does not do so in the holocentric system of Nezara viridula. Here, C-banding and silver impregnation techniques reveal that C-heterochromatin is present in the greater part of the Y chromosome and at the nucleolus organizer region (NOR) of the largest autosome (A 1) and in the extra NOR located in the X chromosome of a single exceptional male. Furthermore, one telomere of each autosome appeared lightly C-banded. The largest, A1, bivalent shows chiasmata almost always located at the chromosome ends. This bivalent may orient axially or equatorially in metaphase I cells depending on whether it carries a single chiasma or two chiasmata, respectively. From our cytological analysis we deduce that centromeric activity is preferentially located at the two telomeric ends and that the presence of chiasmata at an end excludes such activity.Key words: diffuse centromere, C-banding, holocentric, insect chromosomes.


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