Heterochromatin characterization and ribosomal gene location in two monotypic genera of bloodsucker bugs (Cimicidae, Heteroptera) with holokinetic chromosomes and achiasmatic male meiosis
Members of the family Cimicidae (Heteroptera: Cimicomorpha) are temporary bloodsuckers on birds and bats as primary hosts and humans as secondary hosts. Acanthocrios furnarii (2n=12=10+XY, male) and Psitticimex uritui (2n=31=28+X1X2Y, male) are two monotypic genera of the subfamily Haematosiphoninae...
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Cambridge University Press
2014
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| LEADER | 12440caa a22013217a 4500 | ||
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| 001 | PAPER-14767 | ||
| 003 | AR-BaUEN | ||
| 005 | 20250428113614.0 | ||
| 008 | 190411s2014 xx ||||fo|||| 00| 0 eng|d | ||
| 024 | 7 | |2 scopus |a 2-s2.0-84910676411 | |
| 024 | 7 | |2 cas |a Heterochromatin | |
| 030 | |a BEREA | ||
| 040 | |a Scopus |b spa |c AR-BaUEN |d AR-BaUEN | ||
| 100 | 1 | |a Poggio, M.G. | |
| 245 | 1 | 0 | |a Heterochromatin characterization and ribosomal gene location in two monotypic genera of bloodsucker bugs (Cimicidae, Heteroptera) with holokinetic chromosomes and achiasmatic male meiosis |
| 260 | |b Cambridge University Press |c 2014 | ||
| 270 | 1 | 0 | |m Poggio, M.G.; Instituto de Ecología, Genética y Evolución de Buenos Aires (IEGEBA), Ciudad Autónoma de Buenos AiresArgentina |
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| 506 | |2 openaire |e Política editorial | ||
| 520 | 3 | |a Members of the family Cimicidae (Heteroptera: Cimicomorpha) are temporary bloodsuckers on birds and bats as primary hosts and humans as secondary hosts. Acanthocrios furnarii (2n=12=10+XY, male) and Psitticimex uritui (2n=31=28+X1X2Y, male) are two monotypic genera of the subfamily Haematosiphoninae, which have achiasmatic male meiosis of collochore type. Here, we examined chromatin organization and constitution of cimicid holokinetic chromosomes by determining the amount, composition and distribution of constitutive heterochromatin, and number and location of nucleolus organizer regions (NORs) in both species. Results showed that these two bloodsucker bugs possess high heterochromatin content and have an achiasmatic male meiosis, in which three regions can be differentiated in each autosomal bivalent: (i) terminal heterochromatic regions in repulsion; (ii) a central region, where the homologous chromosomes are located parallel but without contact between them; and (iii) small areas within the central region, where collochores are detected. Acanthocrios furnarii presented a single NOR on an autosomal pair, whereas P. uritui presented two NORs, one on an autosomal pair and the other on a sex chromosome. All NORs were found to be associated with CMA3 bright bands, indicating that the whole rDNA repeating unit is rich in G+C base pairs. Based on the variations in the diploid autosomal number, the presence of simple and multiple sex chromosome systems, and the number and location of 18S rDNA loci in the two Cimicidae species studied, we might infer that rDNA clusters and genome are highly dynamic among the representatives of this family. © Cambridge University Press 2014. |l eng | |
| 593 | |a Instituto de Ecología, Genética y Evolución de Buenos Aires (IEGEBA), Ciudad Autónoma de Buenos Aires, Argentina | ||
| 593 | |a Entomología. Departamento de Biodiversidad y Biología Experimental (DBBE), FCEyN, Ciudad Autónoma de Buenos Aires, Argentina | ||
| 650 | 1 | 7 | |2 spines |a BIRD |
| 650 | 1 | 7 | |2 spines |a AVES |
| 690 | 1 | 0 | |a ACHIASMATIC MALE MEIOSIS |
| 690 | 1 | 0 | |a CONSTITUTIVE HETEROCHROMATIN |
| 690 | 1 | 0 | |a HOLOKINETIC CHROMOSOMES |
| 690 | 1 | 0 | |a KARYOTYPE EVOLUTION |
| 690 | 1 | 0 | |a RIBOSOMAL DNA |
| 690 | 1 | 0 | |a CHROMOSOME |
| 690 | 1 | 0 | |a DNA |
| 690 | 1 | 0 | |a GENE EXPRESSION |
| 690 | 1 | 0 | |a INVERTEBRATE |
| 690 | 1 | 0 | |a PEST SPECIES |
| 690 | 1 | 0 | |a SPECIES DIVERSITY |
| 690 | 1 | 0 | |a BAT |
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| 690 | 1 | 0 | |a POLYPLOIDY |
| 690 | 1 | 0 | |a CIMICIDAE |
| 690 | 1 | 0 | |a HETEROPTERA |
| 690 | 1 | 0 | |a CIMICOMORPHA |
| 690 | 1 | 0 | |a HETEROCHROMATIN |
| 690 | 1 | 0 | |a ANIMAL |
| 690 | 1 | 0 | |a CHEMISTRY |
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| 690 | 1 | 0 | |a FLUORESCENCE IN SITU HYBRIDIZATION |
| 690 | 1 | 0 | |a GENETICS |
| 690 | 1 | 0 | |a HETEROCHROMATIN |
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| 690 | 1 | 0 | |a SPECIES DIFFERENCE |
| 690 | 1 | 0 | |a ANIMALS |
| 690 | 1 | 0 | |a CHROMOSOMES, INSECT |
| 690 | 1 | 0 | |a CIMICIDAE |
| 690 | 1 | 0 | |a HETEROCHROMATIN |
| 690 | 1 | 0 | |a IN SITU HYBRIDIZATION, FLUORESCENCE |
| 690 | 1 | 0 | |a KARYOTYPE |
| 690 | 1 | 0 | |a MALE |
| 690 | 1 | 0 | |a MEIOSIS |
| 690 | 1 | 0 | |a SPECIES SPECIFICITY |
| 700 | 1 | |a Di Iorio, O. | |
| 700 | 1 | |a Turienzo, Paola Noemí | |
| 700 | 1 | |a Papeschi, A.G. | |
| 700 | 1 | |a Bressa, M.J. | |
| 773 | 0 | |d Cambridge University Press, 2014 |g v. 104 |h pp. 788-793 |k n. 6 |p Bull. Entomol. Res. |x 00074853 |t Bulletin of Entomological Research | |
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