Polytene chromosomes of three species of blackflies in the Simulium pictipes group (Diptera: Simuliidae)

1975 ◽  
Vol 53 (8) ◽  
pp. 1147-1164 ◽  
Author(s):  
Daniel G. Bedo
Keyword(s):  
Salivary Gland ◽  
Chromosome Number ◽  
Sibling Species ◽  
Sex Chromosomes ◽  
Polytene Chromosomes ◽  
Fluorescence Staining ◽  
Haploid Chromosome Number ◽  
Quinacrine Fluorescence ◽  
Individual Bands ◽  
Staining Methods

The salivary gland chromosomes of members of the Simulium pictipes group were examined by conventional staining and quinacrine fluorescence staining methods which proved to be a useful tool to show otherwise hidden details, especially in expanded centromere regions. Three cytologically definable species were found, one of which must represent a previously unrecognized species. Simulium longistylatum Shewell was the only species among the three siblings identified with certainty. The remaining pair were designated as S. pictipes A and S. pictipes B. In all three siblings the haploid chromosome number was three. Specific differences include a simple and a complex inversion, a shift of basal bands between the short arms of the second and third chromosome, details of the sex chromosomes, and the amount of DNA in certain individual bands and expanded centromere regions. Y chromosome markers are located in a different element of the complement in each of the three species, a unique situation within closely related blackfly sibling species. These findings are discussed in connection with the evolution of sex chromosomes and sibling species. A cytophylogeny is presented.

Genetic and cytogenetic analysis of the fruit fly Rhagoletis cerasi (Diptera: Tephritidae)

Genome ◽  
2008 ◽  
Vol 51 (7) ◽  
pp. 479-491 ◽  
Author(s):  
Ilias Kounatidis ◽  
Nikolaos Papadopoulos ◽  
Kostas Bourtzis ◽  
Penelope Mavragani-Tsipidou
Keyword(s):  
Salivary Gland ◽  
Sex Chromosomes ◽  
Cytogenetic Analysis ◽  
Polytene Chromosomes ◽  
Fruit Fly ◽  
Pest Species ◽  
Heteromorphic Sex Chromosomes ◽  
Weak Points ◽  
Heterogametic Sex ◽  
Rhagoletis Cerasi

The European cherry fruit fly, Rhagoletis cerasi , is a major agricultural pest for which biological, genetic, and cytogenetic information is limited. We report here a cytogenetic analysis of 4 natural Greek populations of R. cerasi, all of them infected with the endosymbiotic bacterium Wolbachia pipientis . The mitotic karyotype and detailed photographic maps of the salivary gland polytene chromosomes of this pest species are presented here. The mitotic metaphase complement consists of 6 pairs of chromosomes, including one pair of heteromorphic sex chromosomes, with the male being the heterogametic sex. The analysis of the salivary gland polytene complement has shown a total of 5 long chromosomes (10 polytene arms) that correspond to the 5 autosomes of the mitotic nuclei and a heterochromatic mass corresponding to the sex chromosomes. The most prominent landmarks of each polytene chromosome, the “weak points”, and the unusual asynapsis of homologous pairs of polytene chromosomes at certain regions of the polytene elements are also presented and discussed.

Cytotaxonomy of Simulium (Montisimulium) ghoomense (Diptera: Simuliidae) from the Darjeeling Hills, India

Zootaxa ◽  
2011 ◽  
Vol 2872 (1) ◽  
pp. 49
Author(s):  
WILLIE HENRY ◽  
SACHIN THAPA ◽  
PETER H. ADLER ◽  
SUBRATA KUMAR DEY ◽  
RAKESH VARMA
Keyword(s):  
Sibling Species ◽  
Sex Chromosomes ◽  
Polytene Chromosomes ◽  
Haploid Number ◽  
Total Complement ◽  
Chromosomal Map

The polytene chromosomes are mapped for a scarce Himalayan simuliid, Simulium (Montisimulium) ghoomense Datta, from the Darjeeling area of India. This species has three tightly paired polytene chromosomes with a haploid number of 3. Chromosomes I, II, and III account for 39.6%, 30.3%, and 30.1% of the total complement length, respectively. The centromeres of chromosomes II and III consistently form a putative partial chromocenter. Sex chromosomes are undifferentiated and polymorphisms and sibling species are lacking in a sample of 35 larvae. This is the first chromosomal map for a species in the subgenus Montisimulium in India.

Sibling species of the blackfly Prosimulium onychodactylum (Simuliidae, Diptera): a salivary gland chromosome study

1983 ◽  
Vol 61 (12) ◽  
pp. 2816-2835 ◽  
Author(s):  
Lester J. Newman
Keyword(s):  
Salivary Gland ◽  
Reproductive Isolation ◽  
Sibling Species ◽  
Chromosome Pairing ◽  
Sex Chromosomes ◽  
Sex Chromosome ◽  
Homologous Pairing ◽  
Chromosome Markers ◽  
Chromosome Arm ◽  
Backcross Hybrids

Larvae of the morphospecies Prosimulium onychodactylum collected from two streams in northern Oregon are divided into 11 sibling species based on fixed and polymorphic inversions. The sibling species have differentiated sex chromosomes; each sibling species falls into one of two groups based on the chromosome arm which carries the sex chromosome markers. Males exhibit lack of homologous pairing or inversion heterzygosity and females have complete chromosome pairing or inversion homozygosity. There is a succession of sibling species which mature in the streams from January through September. Mature larvae of each sibling species are present for about 6 weeks; some are synchronic while others are allochronic. Some of the sibling species occur in the same stream and others are in different streams. Sibling species which are both synchronic and sympatric appear to be reproductively isolated. Reproductive isolation may not be complete for sibling species which are normally allopatric or allochronic; small numbers of F1 and backcross hybrids were found between some of these sibling species. The division of the morphospecies into sibling species was also observed in collections from Washington through northern California.

Sibling species and sex chromosomes in Eusimulium vernum (Diptera: Simuliidae)

1985 ◽  
Vol 63 (9) ◽  
pp. 2145-2161 ◽  
Author(s):  
C. Brockhouse
Keyword(s):  
Sex Determination ◽  
Sibling Species ◽  
Sex Chromosomes ◽  
Polytene Chromosomes ◽  
Biological Species ◽  
Undescribed Species ◽  
Ecological Segregation ◽  
Sex Locus

The polytene chromosomes of larvae from samples of Eusimulium vernum, E. bicorne, and an undescribed species (designated here as Eusimulium "Yukon") were examined. Twelve cytotypes within E. vernum were distinguished, of which at least eight appear to be good biological species. These cytotypes, together with the two allied morphospecies, were related in a cytophylogeny. An ecological segregation between some of the siblings was observed. One cytotype apparently utilizes two (possibly three) separate chromosome (arms) in sex determination. Five of the total of six chromosome arms are involved in sex determination in the various members of this complex. The genetics of sex determination and the mechanisms of sex-locus shift are discussed in the context of these findings.

scholarly journals A long reads-based de-novo assembly of the genome of the Arlee homozygous line reveals chromosomal rearrangements in rainbow trout

2021 ◽  
Author(s):  
Guangtu Gao ◽  
Susana Magadan ◽  
Geoffrey C Waldbieser ◽  
Ramey C Youngblood ◽  
Paul A Wheeler ◽  
...  
Keyword(s):  
Rainbow Trout ◽  
Chromosome Number ◽  
Genome Assembly ◽  
De Novo Assembly ◽  
De Novo ◽  
Sequence Data ◽  
Structural Variations ◽  
High Coverage ◽  
Haploid Chromosome Number ◽  
Long Reads

Abstract Currently, there is still a need to improve the contiguity of the rainbow trout reference genome and to use multiple genetic backgrounds that will represent the genetic diversity of this species. The Arlee doubled haploid line was originated from a domesticated hatchery strain that was originally collected from the northern California coast. The Canu pipeline was used to generate the Arlee line genome de-novo assembly from high coverage PacBio long-reads sequence data. The assembly was further improved with Bionano optical maps and Hi-C proximity ligation sequence data to generate 32 major scaffolds corresponding to the karyotype of the Arlee line (2 N = 64). It is composed of 938 scaffolds with N50 of 39.16 Mb and a total length of 2.33 Gb, of which ∼95% was in 32 chromosome sequences with only 438 gaps between contigs and scaffolds. In rainbow trout the haploid chromosome number can vary from 29 to 32. In the Arlee karyotype the haploid chromosome number is 32 because chromosomes Omy04, 14 and 25 are divided into six acrocentric chromosomes. Additional structural variations that were identified in the Arlee genome included the major inversions on chromosomes Omy05 and Omy20 and additional 15 smaller inversions that will require further validation. This is also the first rainbow trout genome assembly that includes a scaffold with the sex-determination gene (sdY) in the chromosome Y sequence. The utility of this genome assembly is demonstrated through the improved annotation of the duplicated genome loci that harbor the IGH genes on chromosomes Omy12 and Omy13.

Genetic Analysis of the Drosophila 63F Early Puff: Characterization of Mutations in E63-1 and maggie, a Putative Tom22

Genetics ◽  
2000 ◽  
Vol 156 (1) ◽  
pp. 229-244
Author(s):  
Martina Vaskova ◽  
A M Bentley ◽  
Samantha Marshall ◽  
Pamela Reid ◽  
Carl S Thummel ◽  
...  
Keyword(s):  
Salivary Gland ◽  
Genetic Analysis ◽  
Polytene Chromosomes ◽  
Reading Frame ◽  
Protein Levels ◽  
Ef Hand ◽  
Larval Salivary Gland ◽  
Complementation Groups ◽  
Inducible Genes ◽  
Early Puff

Abstract The 63F early puff in the larval salivary gland polytene chromosomes contains the divergently transcribed E63-1 and E63-2 ecdysone-inducible genes. E63-1 encodes a member of the EF-hand family of Ca2+-binding proteins, while E63-2 has no apparent open reading frame. To understand the functions of the E63 genes, we have determined the temporal and spatial patterns of E63-1 protein expression, as well as undertaken a genetic analysis of the 63F puff. We show that E63-1 is expressed in many embryonic and larval tissues, but the third-instar larval salivary gland is the only tissue where increases in protein levels correlate with increases in ecdysone titer. Furthermore, the subcellular distribution of E63-1 protein changes dynamically in the salivary glands at the onset of metamorphosis. E63-1 and E63-2 null mutations, however, have no effect on development or fertility. We have characterized 40 kb of the 63F region, defined as the interval between Ubi-p and E63-2, and have identified three lethal complementation groups that correspond to the dSc-2, ida, and mge genes. We show that mge mutations lead to first-instar larval lethality and that Mge protein is similar to the Tom22 mitochondrial import proteins of fungi, suggesting that it has a role in mitochondrial function.

A modification of Heidenhain's iron-haematoxylin technique, as used to stain smears of Drosophila larval polytene chromosomes and neuroblast cells

1971 ◽  
Vol 49 (1) ◽  
pp. 132-133 ◽  
Author(s):  
Albert E. Moorman
Keyword(s):  
Acetic Acid ◽  
Salivary Gland ◽  
Methyl Alcohol ◽  
Polytene Chromosomes ◽  
Larval Salivary Gland

Acetic-acid-fixed smears of Drosophila larval salivary gland chromosomes and of neuroblast cells from the larval ganglion undergoing mitosis are prepared by a modification of Heidenhain's iron-haematoxylin technique, in which absolute methyl alcohol is the solvent of all reagents used in the staining process.

scholarly journals Chromosomal and DNA barcode analysis of the Melitaea ala Staudinger, 1881 species complex (Lepidoptera, Nymphalidae)

2021 ◽  
Vol 15 (2) ◽  
pp. 199-216
Author(s):  
Vladimir A. Lukhtanov ◽  
Anastasia V. Gagarina ◽  
Elena A. Pazhenkova
Keyword(s):  
Chromosome Number ◽  
Central Asia ◽  
Species Complex ◽  
Dna Barcode ◽  
Monophyletic Group ◽  
Geographic Proximity ◽  
Haploid Chromosome Number ◽  
East Central ◽  
North East ◽  
Peter The Great

The species of the Melitaea ala Staudinger, 1881 complex are distributed in Central Asia. Here we show that this complex is a monophyletic group including the species, M. ala, M. kotshubeji Sheljuzhko, 1929 and M. enarea Fruhstorfer, 1917. The haploid chromosome number n=29 is found in M. ala and M. kotshubeji and is, most likely, a symplesiomorphy of the M. ala complex. We show that M. ala consists of four subspecies: M. ala zaisana Lukhtanov, 1999 (=M. ala irtyshica Lukhtanov, 1999, syn. nov.) (South Altai, Zaisan Lake valley), M. ala ala (Dzhungarian Alatau), M. ala bicolor Seitz, 1908 (North, East, Central and West Tian-Shan) and M. ala determinata Bryk, 1940 (described from “Fu-Shu-Shi”, China). We demonstrate that M. kotshubeji kotshubeji (Peter the Great Mts in Tajikistan) and M. kotshubeji bundeli Kolesnichenko, 1999 (Alai Mts in Tajikistan and Kyrgyzstan) are distinct taxa despite their geographic proximity in East Tajikistan. Melitaea enarea is widely distributed in the southern part of Central Asia and is sympatric with M. kotshubeji.

scholarly journals One more Microtus species with asynaptic sex chromosomes

2018 ◽  
Vol 70 (3) ◽  
pp. 443-447
Author(s):  
Jelena Blagojevic ◽  
Marija Rajicic ◽  
Vladimir Jovanovic ◽  
Tanja Adnadjevic ◽  
Ivana Budinski ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Sex Chromosomes ◽  
Diploid Chromosome Number ◽  
First Finding ◽  
Chromosomal Polymorphisms ◽  
Southeastern Serbia

Arvicoline voles are known as a karyotypically extremely polymorphic group in which the genus Microtus leads with the highest rate of karyotype change. A member of this genus, the European pine vole Microtus subterraneus (de Selys-Longchamps, 1836), is widely distributed in Europe and parts of Asia. There are two cytotypes differing in diploid chromosome number, 2n=54 and 52, each showing different chromosomal polymorphisms. At two localities in southeastern Serbia, Mt. Jastrebac and Vlasina, we found the 2n=52 cytotype. Meiotic preparations from males revealed the presence of asynaptic sex chromosomes. Although asynaptic sex chromosomes are frequent in Microtus, this is the first finding for M. subterraneus. From summarized data it appears that two-thirds of the studied species, mainly from Microtus and Terricola subgenera, possess asynaptic sex chromosomes.

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