Chromosomal rearrangements in rock wallabies, Petrogale (Marsupialia: Macropodidae). IX. Further G-banding studies of the Petrogale lateralis complex: P. lateralis pearsoni, the West Kimberley race, and a population heterozygous for a centric fusion

Genome ◽  
1997 ◽  
Vol 40 (1) ◽  
pp. 84-90 ◽  
Author(s):  
M. D. B. Eldridge ◽  
D. J. Pearson

G-banded metaphase preparations from cultured fibroblasts were used to examine the karyotypes of Petrogale lateralis pearsoni and the West Kimberley (WK) race of P. lateralis. Petrogale lateralis pearsoni was found to retain the ancestral 2n = 22 Petrogale karyotype, while the WK race (2n = 20) was found to be characterized by a 9–10 centric fusion. This taxon had been reported to have an 8–10 fusion. Karyotypic analysis was also used to identify Petrogale populations in the Erskine Range, Western Australia (W.A.) as the WK race and in the Walter James Range, W.A. as the MacDonnell Ranges (MDR) race of P. lateralis. These findings represent significant range extensions for both taxa. A third P. lateralis population, from the Townsend Ridges, W.A., could not be definitively identified to subspecies or race and appears intermediate between the WK and MDR races. Four animals were examined from this population and all possessed an identical 2n = 21 karyotype characterized by homozygosity for a derived acrocentric chromosome 3 (3a) and heterozygosity for a 9–10 fusion. Rearrangement 3a is typical of the MDR race, while the 9–10 fusion is characteristic of the WK race. The polymorphic Townsend Ridges population could result from the de novo creation of a 9–10 fusion (similar in morphology to the 9–10 fusion of the WK race) or it may represent evidence of hybridization between the MDR race and either the WK race or a currently unknown taxon. Additional data will be required to distinguish between these hypotheses.Key words: rock wallabies, Petrogale, chromosome rearrangements, G-banding.

Genome ◽  
1990 ◽  
Vol 33 (6) ◽  
pp. 798-802 ◽  
Author(s):  
M. D. B. Eldridge ◽  
R. L. Close ◽  
P. G. Johnston

The karyotypes of Petrogale inornata and the two currently recognised races of Petrogale penicillata were examined using G-banding from cultured fibroblasts. Petrogale inornata (2n = 22) was found to retain plesiomorphic chromosomes 3 and 4 but possessed an apomorphic inverted chromosome 5 (5i). This 5i appears identical with the 5i found in two other Queensland taxa, Petrogale assimilis and Petrogale godmani, and can be derived from the ancestral chromosome 5 by an extensive paracentric inversion or a centromeric transposition. Petrogale penicillata penicillata (2n = 22) and Petrogale penicillata herberti (2n = 22) both possess the synapomorphic acrocentric chromosome 3, which appears to differ from the plesiomorphic 3 by a small centromeric transposition. Petrogale p. penicillata was also found to be characterised by an apomorphic acrocentric chromosome 4, while P. p. herberti was characterised by an autapomorphic submetacentric chromosome 4. Both apomorphic chromosomes 4 can be related to the plesiomorphic chromosome 4 by centromeric transpositions. Thus although P. inornata is chromosomally distinct it is more closely related to other north Queensland taxa than it is to either P. p. penicillata or P. p. herberti.Key words: chromosomal rearrangements, G-banding, Marsupialia, Petrogale, Macropodidae.


1991 ◽  
Vol 39 (6) ◽  
pp. 621 ◽  
Author(s):  
MDB Eldridge ◽  
RL Close ◽  
PG Johnston

The karyotypes of Petrogale lateralis lateralis, P. l. purpureicollis and P. l 'Macdonnell Ranges' were examined with G-banding from cultured fibroblasts. P. l. lateralis (2n = 22) was found to retain the plesiomorphic karyotype, whereas P. l. purpureicollis (2n = 22) and P. l. 'Macdonnell Ranges' (2n = 22) were found to share an apomorphic karyotype characterised by an acrocentric chromosome 3 (3a) and an acrocentric X-chromosome (Xp). Both the 3a and Xp can be derived from their respective P. l. lateralis homologues by centric transpositions. Although P. l. purpureicollis and P. l. 'Macdonnell Ranges' appear very similar chromosomally, they are readily distinguishable genically and morphologically, P. l. 'Macdonnell Ranges' being more similar to P. l. lateralis. Thus, in these taxa, genic and morphological divergence have not been associated with significant changes in karyotype.


2018 ◽  
Vol 16 (05) ◽  
pp. 362-368 ◽  
Author(s):  
Federica Sullo ◽  
Agata Polizzi ◽  
Stefano Catanzaro ◽  
Selene Mantegna ◽  
Francesco Lacarrubba ◽  
...  

Cerebellotrigeminal dermal (CTD) dysplasia is a rare neurocutaneous disorder characterized by a triad of symptoms: bilateral parieto-occipital alopecia, facial anesthesia in the trigeminal area, and rhombencephalosynapsis (RES), confirmed by cranial magnetic resonance imaging. CTD dysplasia is also known as Gómez-López-Hernández syndrome. So far, only 35 cases have been described with varying symptomatology. The etiology remains unknown. Either spontaneous dominant mutations or de novo chromosomal rearrangements have been proposed as possible explanations. In addition to its clinical triad of RES, parietal alopecia, and trigeminal anesthesia, CTD dysplasia is associated with a wide range of phenotypic and neurodevelopmental abnormalities.Treatment is symptomatic and includes physical rehabilitation, special education, dental care, and ocular protection against self-induced corneal trauma that causes ulcers and, later, corneal opacification. The prognosis is correlated to the mental development, motor handicap, corneal–facial anesthesia, and visual problems. Follow-up on a large number of patients with CTD dysplasia has never been reported and experience is limited to few cases to date. High degree of suspicion in a child presenting with characteristic alopecia and RES has a great importance in diagnosis of this syndrome.


2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Marcelo Razera Baruffi ◽  
Deise Helena de Souza ◽  
Rosana Aparecida Bicudo da Silva ◽  
Ester Silveira Ramos ◽  
Danilo Moretti-Ferreira

Balanced X-autosome translocations are rare, and female carriers are a clinically heterogeneous group of patients, with phenotypically normal women, history of recurrent miscarriage, gonadal dysfunction, X-linked disorders or congenital abnormalities, and/or developmental delay. We investigated a patient with ade novoX;19 translocation. The six-year-old girl has been evaluated due to hyperactivity, social interaction impairment, stereotypic and repetitive use of language with echolalia, failure to follow parents/caretakers orders, inconsolable outbursts, and persistent preoccupation with parts of objects. The girl has normal cognitive function. Her measurements are within normal range, and no other abnormalities were found during physical, neurological, or dysmorphological examinations. Conventional cytogenetic analysis showed ade novobalanced translocation, with the karyotype 46,X,t(X;19)(p21.2;q13.4). Replication banding showed a clear preference for inactivation of the normal X chromosome. The translocation was confirmed by FISH and Spectral Karyotyping (SKY). Although abnormal phenotypes associated withde novobalanced chromosomal rearrangements may be the result of disruption of a gene at one of the breakpoints, submicroscopic deletion or duplication, or a position effect, X; autosomal translocations are associated with additional unique risk factors including X-linked disorders, functional autosomal monosomy, or functional X chromosome disomy resulting from the complex X-inactivation process.


Genome ◽  
2003 ◽  
Vol 46 (2) ◽  
pp. 291-303 ◽  
Author(s):  
I A.P Parkin ◽  
A G Sharpe ◽  
D J Lydiate

The progenitor diploid genomes (A and C) of the amphidiploid Brassica napus are extensively duplicated with 73% of genomic clones detecting two or more duplicate sequences within each of the diploid genomes. This comprehensive duplication of loci is to be expected in a species that has evolved through a polyploid ancestor. The majority of the duplicate loci within each of the diploid genomes were found in distinct linkage groups as collinear blocks of linked loci, some of which had undergone a variety of rearrangements subsequent to duplication, including inversions and translocations. A number of identical rearrangements were observed in the two diploid genomes, suggesting they had occurred before the divergence of the two species. A number of linkage groups displayed an organization consistent with centric fusion and (or) fission, suggesting this mechanism may have played a role in the evolution of Brassica genomes. For almost every genetically mapped locus detected in the A genome a homologous locus was found in the C genome; the collinear arrangement of these homologous markers allowed the primary regions of homoeology between the two genomes to be identified. At least 16 gross chromosomal rearrangements differentiated the two diploid genomes during their divergence from a common ancestor.Key words: genome evolution, Brassicaeae, polyploidy, homoeologous linkage groups.


2001 ◽  
Vol 10 (3) ◽  
pp. 193-196 ◽  
Author(s):  
T. Sudha ◽  
A. J. Dawson ◽  
A. N. Prasad ◽  
D. Konkin ◽  
G. W. de Groot ◽  
...  

2017 ◽  
Author(s):  
Thomas Blankers ◽  
Kevin P. Oh ◽  
Aureliano Bombarely ◽  
Kerry L. Shaw

ABSTRACTPhenotypic evolution and speciation depend on recombination in many ways. Within populations, recombination can promote adaptation by bringing together favorable mutations and decoupling beneficial and deleterious alleles. As populations diverge, cross-over can give rise to maladapted recombinants and impede or reverse diversification. Suppressed recombination due to genomic rearrangements, modifier alleles, and intrinsic chromosomal properties may offer a shield against maladaptive gene flow eroding co-adapted gene complexes. Both theoretical and empirical results support this relationship. However, little is known about this relationship in the context of behavioral isolation, where co-evolving signals and preferences are the major hybridization barrier. Here we examine the genomic architecture of recently diverged, sexually isolated Hawaiian swordtail crickets (Laupala). We assemble a de novo genome and generate three dense linkage maps from interspecies crosses. In line with expectations based on the species’ recent divergence and successful interbreeding in the lab, the linkage maps are highly collinear and show no evidence for large-scale chromosomal rearrangements. The maps were then used to anchor the assembly to pseudomolecules and estimate recombination rates across the genome. We tested the hypothesis that loci involved in behavioral isolation (song and preference divergence) are in regions of low interspecific recombination. Contrary to our expectations, a genomic region where a male song QTL co-localizes with a female preference QTL was not associated with particularly low recombination rates. This study provides important novel genomic resources for an emerging evolutionary genetics model system and suggests that trait-preference co-evolution is not necessarily facilitated by locally suppressed recombination.


1992 ◽  
Vol 19 (4) ◽  
pp. 405 ◽  
Author(s):  
NJ Gales ◽  
AJ Cheal ◽  
GJ Pobar ◽  
P Williamson

The Australian sea-lion, Neophoca cinerea, has a 17-18-month breeding cycle on islands off the west coast of Western Australia. Buller, North Fisherman and Beagle Is are the main pupping sites, with several very small colonies (n> 3) at the Abrolhos Is. The 4-5-month pupping seasons are synchronised at North Fisherman and Beagle Is, but the sea-lions from Buller I. breed one month later and those from the Abrolhos Is two months earlier. Pup production and pup mortality were highly variable between seasons over which observations were recorded: 129 pups were born at the main breeding sites in early 1988, the mortality in the first five months was 7.1%, whereas 181 pups were born in late 1989 of which 24.3% died. Pups remain in the vicinity of their natal islands for the first 4-5 months of life before leaving, perhaps on foraging trips, with their mothers. Most return to their natal island, although others haulout on islands up to 27 km away. Some male N. cinerea congregate in bachelor colonies on islands adjacent to the Perth metropolitan region during the non-breeding season and migrate up to 280 km north each breeding season. The status of the isolated, west-coast N. cinerea population is unknown. The current high level of human pressure on sea-lion terrestrial habitats and their food resources indicate a need for further monitoring of this species.


2018 ◽  
Vol 102 (6) ◽  
pp. 1090-1103 ◽  
Author(s):  
Christina Halgren ◽  
Nete M. Nielsen ◽  
Lusine Nazaryan-Petersen ◽  
Asli Silahtaroglu ◽  
Ryan L. Collins ◽  
...  

Koedoe ◽  
1995 ◽  
Vol 38 (2) ◽  
Author(s):  
J. Heyns

Acrobeles fananae spec. nov. is described from two localities on the west coast of South Africa. The new species is characterised by body length of 0.7-0.8 mm; relatively slender, cylindroid body, abruptly ventrally bent in vulval region; vulva with protruding lips and situated in a sunken area; three incisures in lateral field; and cuticle with an intricate interlocked block-like pattern. Additional data is presented on the morphology of Seleborca complexa (Thorne, 1925) collected in the same area.


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