Studies of the X chromosome of Anopheles albimanus

1985 ◽  
Vol 27 (1) ◽  
pp. 74-82
Author(s):  
J. A. Seawright ◽  
M. Q. Benedict ◽  
S. Narang

Snow (sn) is a recessive, eye color mutant that is phenotypically indistinguishable from the previously described mutant, white eye (we). The loci for these mutants are over 30 map units apart on the X chromosome. Analysis of salivary gland chromosomes of radiation-induced X-autosome translocations were used to define the positions of sn and we on the distal euchromatic portion of the long arm of the X chromosome. A recessive lethal trait (bubble head) was also mapped relative to we and sn, and the gene order on the long arm of the X chromosome is as follows: centromere – ? – snow – bubble head – white eye. Translocation breakpoints in the euchromatic portion of the X chromosome caused sterility or lethality in males hemizygous for the translocations, but breaks in the heterochromatin had no effect. Crossing-over was greatly reduced when translocation breakpoints were located in the euchromatic part of the X chromosome. The translocations were used to determine that the nucleolar organizer region is probably on the short arm of the X chromosome.Key words: Anopheles albimanus, eye colour mutant, X chromosome.

1994 ◽  
Vol 6 (4) ◽  
pp. 533 ◽  
Author(s):  
ES Robinson ◽  
PB Samollow ◽  
JL VandeBerg ◽  
PG Johnston

Somatic cells from the opossums Monodelphis domestica and Didelphis virginiana were labelled with 5-bromodeoxyuridine (BrdU), treated with colchicine, stained with acridine orange and examined using fluorescence microscopy. BrdU-incorporated metaphase spreads from females of M. domestica at developmental stages from late bilaminar blastocysts to adults showed replication asynchrony of the two (acrocentric) X chromosomes. The long arm of one X chromosome was the latest replicating region in the entire chromosome complement and is presumed to represent transcriptional inactivation and X dosage compensation. The minute short arm of the same X, which contains a nucleolar organizer region, was earlier replicating and synchronous with the short arm of its homologue and is thus assumed to escape inactivation. BrdU-incorporated spreads from cells of fetuses, neonates and adults of D. virginiana also showed a late replicating (submetacentric) X chromosome. The pattern was different from that of M. domestica because of the different morphology and the presence of large blocks of constitutive heterochromatin in both homologues. The timing and pattern of replication of the single X in males of both species resembled the earlier replicating X in females. The array of molecular techniques now available offers the best means for investigating X-chromosome replication and activity states of X-linked genes in the earliest stages of marsupial embryogenesis.


2020 ◽  
Vol 21 (9) ◽  
Author(s):  
MANACHAYA PISSAPARN ◽  
SUMALEE PHIMPHAN ◽  
PATCHARAPORN CHAIYASAN ◽  
ALONGKLOD TANOAMTONG ◽  
THOMAS LIEHR ◽  
...  

Abstract. Pissaparn M, Phimphan S, Chaiyasan P, Tanoamtong A, Liehr T, Suwannapoom C, Reungsing M, Supiwong W. 2020. First chromosome analysis of Thai pufferfish Pao cochinchinensis (Steindachner, 1866). Biodiversitas 21: 4309-4316. Here first analysis of chromosomes and nucleolar organizer region (NOR) pattern in pufferfish Pao cochinchinensis (Steindachner, 1866) was undertaken. Chromosomal preparations were obtained from kidney of P. cochinchinensis from Chi River basin in Thailand. Chromosomal characteristics were analyzed by Giemsa staining, Ag-NOR banding as well as fluorescence in situ hybridization (FISH) using microsatellites d(CA)15 and d(CGG)10 probes. P. cochinchinensis had 2n = 40 with the fundamental number (NF) 74, both in male and female. The karyotype exhibited 12 metacentric (m), 10 submetacentric (sm), 12 acrocentric (a) and 6 telocentric (t) chromosomes. No differentiated heteromorphic sex chromosomes were observed. NORs were located on short arms adjacent to telomere of the metacentric chromosome pair 4, which coincide with signals of d(CGG)10 probe. FISH with d(CGG)10 sequences were also displayed at the telomeres of most other chromosomes, whereas d(CA)15 repeats highly accumulated throughout almost all entire chromosomes except for centromeric regions. The results of conventional Giemsa staining presented the differentiation even the same genus. The localization of NORs on one pair of chromosomes only is a common characteristic found in many fish groups as well as other vertebrates. Mapping of two distinct microsatellites demonstrated the remarkable chromosomal diversification that characterizes evolution in the genus Pao. Both, conventional and molecular cytogenetics are excellent tools to study, and better understand chromosomal evolution, as well as to uncover biodiversity among fishes.


CYTOLOGIA ◽  
2013 ◽  
Vol 78 (3) ◽  
pp. 213-222 ◽  
Author(s):  
Wilailuk Khrueanet ◽  
Weerayuth Supiwong ◽  
Chanidaporn Tumpeesuwan ◽  
Sakboworn Tumpeesuwan ◽  
Krit Pinthong ◽  
...  

2020 ◽  
pp. 1-6
Author(s):  
Ross Brookwell ◽  
Kimberly Finlayson ◽  
Jason P. van de Merwe

The karyotype of the Odontocete whale, <i>Mesoplodon densirostris</i>, has not been previously reported. The chromosome number is determined to be 2n = 42, and the karyotype is presented using G-, C-, and nucleolar organizer region (NOR) banding. The findings include NOR regions on 2 chromosomes, regions of heterochromatic variation, a large block of heterochromatin on the X chromosome, and a relatively large Y chromosome. The karyotype is compared to published karyograms of 2 other species of <i>Mesoplodon</i>.


Genome ◽  
1988 ◽  
Vol 30 (5) ◽  
pp. 656-663 ◽  
Author(s):  
J. Gosálvez ◽  
C. López-Fernández ◽  
L. J. Bella ◽  
R. K. Butlin ◽  
G. M. Hewitt

Two subspecies of the meadow grasshopper Chorthippus parallelus form narrow hybrid zones in the Pyrenees. We studied the patterns of chromosome divergence to evaluate their possible role in the maintenance of such hybrid zones under natural conditions. The two subspecies share some common features such as identical chromosome number, similar basic chromosome form, and the GC-rich nature of all the heterochromatic DNA. Similar positions for the nucleolar organizer region (NOR) in two pairs of autosomes were also observed. The main difference was the presence of an active NOR in the X chromosome in Cp. parallelus that was absent from Cp. erythropus. The pattern of banding by C-banding, acridine orange, and chromomycin A3 also showed the subspecific characteristics on this chromosome. The presence or absence of an active NOR on the X chromosome was used to analyse the hybrid zones in two different transects of the Pyrenees, and clear clines of X NOR frequencies were observed passing from Cp. parallelus to Cp. erythropus. Some meiotic abnormalities were found in individuals from the hybrid zones with the subsequent production of abnormal sperm. Differences in genetic activity involving the sexual chromosome and the male sterility found in F1 hybrids produced in laboratory crosses are discussed as an example of Haldane's Rule.Key words: insect cytogenetics, hybrid zones, speciation.


CYTOLOGIA ◽  
2014 ◽  
Vol 79 (1) ◽  
pp. 3-14 ◽  
Author(s):  
Sitthisak Jantarat ◽  
Sumpars Khunsook ◽  
Praween Supanuam ◽  
Somsak Jeewattana ◽  
Sarawut Kaewsri ◽  
...  

2021 ◽  
Vol 43 (3) ◽  
pp. 237-249 ◽  
Author(s):  
Thanh Dat Ta ◽  
Nomar Espinosa Waminal ◽  
Thi Hong Nguyen ◽  
Remnyl Joyce Pellerin ◽  
Hyun Hee Kim

Abstract Background DNA tandem repeats (TRs) are often abundant and occupy discrete regions in eukaryotic genomes. These TRs often cause or generate chromosomal rearrangements, which, in turn, drive chromosome evolution and speciation. Tracing the chromosomal distribution of TRs could therefore provide insights into the chromosome dynamics and speciation among closely related taxa. The basic chromosome number in the genus Senna is 2n = 28, but dysploid species like Senna tora have also been observed. Objective To understand the dynamics of these TRs and their impact on S. tora dysploidization. Methods We performed a comparative fluorescence in situ hybridization (FISH) analysis among nine closely related Senna species and compared the chromosomal distribution of these repeats from a cytotaxonomic perspective by using the ITS1-5.8S-ITS2 sequence to infer phylogenetic relationships. Results Of the nine S. tora TRs, two did not show any FISH signal whereas seven TRs showed similar and contrasting patterns to other Senna species. StoTR01_86, which was localized in the pericentromeric regions in all S. tora, but not at the nucleolar organizer region (NOR) site, was colocalized at the NOR site in all species except in S. siamea. StoTR02_7_tel was mostly localized at chromosome termini, but some species had an interstitial telomeric repeat in a few chromosomes. StoTR05_180 was distributed in the subtelomeric region in most species and was highly amplified in the pericentromeric region in some species. StoTR06_159 was either absent or colocalized in the NOR site in some species, and StoIGS_463, which was localized at the NOR site in S. tora, was either absent or localized at the subtelomeric or pericentromeric regions in other species. Conclusions These data suggest that TRs play important roles in S. tora dysploidy and suggest the involvement of 45S rDNA intergenic spacers in “carrying” repeats during genome reshuffling.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Jung-Hyun Kim ◽  
Vladimir N. Noskov ◽  
Aleksey Y. Ogurtsov ◽  
Ramaiah Nagaraja ◽  
Nikolai Petrov ◽  
...  

AbstractThe rDNA clusters and flanking sequences on human chromosomes 13, 14, 15, 21 and 22 represent large gaps in the current genomic assembly. The organization and the degree of divergence of the human rDNA units within an individual nucleolar organizer region (NOR) are only partially known. To address this lacuna, we previously applied transformation-associated recombination (TAR) cloning to isolate individual rDNA units from chromosome 21. That approach revealed an unexpectedly high level of heterogeneity in human rDNA, raising the possibility of corresponding variations in ribosome dynamics. We have now applied the same strategy to analyze an entire rDNA array end-to-end from a copy of chromosome 22. Sequencing of TAR isolates provided the entire NOR sequence, including proximal and distal junctions that may be involved in nucleolar function. Comparison of the newly sequenced rDNAs to reference sequence for chromosomes 22 and 21 revealed variants that are shared in human rDNA in individuals from different ethnic groups, many of them at high frequency. Analysis infers comparable intra- and inter-individual divergence of rDNA units on the same and different chromosomes, supporting the concerted evolution of rDNA units. The results provide a route to investigate further the role of rDNA variation in nucleolar formation and in the empirical associations of nucleoli with pathology.


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