Gametangial meiosis in Phytophthora capsici

1976 ◽  
Vol 54 (13) ◽  
pp. 1535-1545 ◽  
Author(s):  
E. Sansome
Keyword(s):  
Chromosome Number ◽  
Phytophthora Capsici ◽  
Nuclear Size ◽  
Chromosome Size ◽  
Chromosome Counts ◽  
Haploid Chromosome Number ◽  
Zygote Nucleus ◽  
Gametangial Meiosis

The report of Stephenson et al. that the nuclear divisions in the gametangia of Phytophthora capsici are mitotic, resembling the divisions in the vegetative hyphae, was not confirmed. Pachytene, diplotene, and diakinesis stages were observed in the oogonia. Metaphase and anaphase were followed by a second division without any increase in nuclear and chromosome size between the two divisions. The haploid chromosome number is nine and an association of four chromosomes is present in one or both parents.The association of four chromosomes observed at diakinesis and metaphase is evidence that pairing of homologous parts occurs during the first division and is thus proof that the gametangial divisions are meiotic.There was no evidence of a prolonged prophase in the first division of the zygote nucleus and an eight-nucleate oospore showed no evidence of reduction in nuclear size or nuclear elimination such as would be required to account for the homokaryotic condition of single-oospore cultures on the hypothesis of zygotic meiosis.The problems involved in obtaining reliable chromosome counts from somatic nuclei are discussed.

scholarly journals Unprecedented reorganization of holocentric chromosomes provides insights into the enigma of lepidopteran chromosome evolution

2019 ◽  
Vol 5 (6) ◽  
pp. eaau3648 ◽  
Author(s):  
Jason Hill ◽  
Pasi Rastas ◽  
Emily A. Hornett ◽  
Ramprasad Neethiraj ◽  
Nathan Clark ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Chromosome Evolution ◽  
Chromosome Structure ◽  
Holocentric Chromosomes ◽  
Chromosome Counts ◽  
Pieris Napi ◽  
Haploid Chromosome Number ◽  
Genome Wide ◽  
The Face ◽  
Chromosome Level

Chromosome evolution presents an enigma in the mega-diverse Lepidoptera. Most species exhibit constrained chromosome evolution with nearly identical haploid chromosome counts and chromosome-level gene collinearity among species more than 140 million years divergent. However, a few species possess radically inflated chromosomal counts due to extensive fission and fusion events. To address this enigma of constraint in the face of an exceptional ability to change, we investigated an unprecedented reorganization of the standard lepidopteran chromosome structure in the green-veined white butterfly (Pieris napi). We find that gene content in P. napi has been extensively rearranged in large collinear blocks, which until now have been masked by a haploid chromosome number close to the lepidopteran average. We observe that ancient chromosome ends have been maintained and collinear blocks are enriched for functionally related genes suggesting both a mechanism and a possible role for selection in determining the boundaries of these genome-wide rearrangements.

Recherches sur les Alaria (Phaeophyceae) de l'est canadien. I. Nombres chromosomiques et identité des Alaria de l'estuaire du St-Laurent

1974 ◽  
Vol 52 (4) ◽  
pp. 691-694 ◽  
Author(s):  
M.-J. Feller-Demalsy ◽  
P. Demalsy
Keyword(s):  
Chromosome Number ◽  
Single Species ◽  
Chromosome Counts ◽  
Eastern Canada ◽  
Lawrence Estuary ◽  
Haploid Chromosome Number ◽  
Biosystematic Study ◽  
Alaria Esculenta ◽  
St Lawrence Estuary

Chromosome counts in gametophytes and sporophylls of Alaria collected in the St. Lawrence Estuary show that all the specimens of this genus in eastern Canada may not belong to the single species A. esculenta Greville. Indeed, the haploid chromosome number (n) found in these algae is equal to half of the number attributed in the literature to Alaria esculenta from the British coasts. Three hypotheses for the interpretation of these observations are considered. The solution of the problem of the identity of Alaria can only be hoped for from their global, morphological, and biosystematic study.

Meiotic configurations in the oospore of Phytophthora capsici

1974 ◽  
Vol 52 (10) ◽  
pp. 2141-2143 ◽  
Author(s):  
L. W. Stephenson ◽  
D. C. Erwin ◽  
J. V. Leary
Keyword(s):  
Phytophthora Capsici ◽  
Nuclear Size ◽  
Chromosome Size ◽  
Haploid Number ◽  
Whole Mounts ◽  
Metaphase I

Photomicrographs of chromosomal configurations in nuclei of squashed whole mounts of mature oospores (cultures 32 days old) of Phytophthora capsici stained with iron hematoxylin were interpreted to indicate that meiosis occurred in the oospore. Chromosomes in dividing oospore nuclei were observed in synapsis, diakinesis, metaphase I, and metaphase II. Comparison of polar metaphase I and metaphase II plates revealed a reduction in chromosome size and number and nuclear size. The haploid number of chromosomes was interpreted to be 6.

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.

The early development of haploid and aneuploid parthenogenetic embryos

Development ◽  
1975 ◽  
Vol 34 (3) ◽  
pp. 645-655
Author(s):  
Matthew H. Kaufman ◽  
Leo Sachs
Keyword(s):  
Early Development ◽  
Polar Body ◽  
Chromosome Counts ◽  
Cell Stage ◽  
Haploid Chromosome Number ◽  
Stage Of Development ◽  
Morula Stage ◽  
Second Polar Body ◽  
Similar Development ◽  
Parthenogenetic Embryos

The early development of parthenogenetically activated oocytes has been studied in C57BL × CBA-T6T6 (F1T6) translocation heterozygote mice and C57BL × CBA-LAC (F1LAC) mice. All F1T6 oocytes had either a quadrivalent or a univalent-trivalent configuration at meiosis I; no such chromosome configurations were observed in the F1LAC oocytes. At ovulation 36·5 % of the F1T6 oocytes had 19 or 21 chromosomes, whereas 97 % of the F1LAC had the normal haploid chromosome number of 20. After parthenogenetic activation, chromosome counts at metaphase of the first cleavage mitosis were made of the eggs with a single pronucleus following extrusion of the second polar body. These activated eggs had similar frequencies of 19, 20 and 21 chromosomes as had the oocytes at ovulation. The activated 1-cell eggs were transferred to the oviducts of pseudopregnant recipients and the embryos recovered 3 days later. At this stage of development, most of the F1T6 embryos with 19 chromosomes were no longer found, but the frequency of 21-chromosome embryos was similar to the frequency of 21-chromosome oocytes and activated eggs. There was a similar mean number of cells in the embryos with 20 and 21 chromosomes. The results indicate that nearly all the embryos with 19 chromosomes failed to develop, probably beyond the 2-cell stage, whereas oocytes with 21 chromosomes had a similar development to oocytes with 20 chromosomes up to the morula stage.

Chromatin Diminution in Cyclops kolensis Lill. (Copepoda, Crustacea) as a Radical Way to Inactivate Redundant Genome in Somatic Cells

2018 ◽  
Vol 156 (3) ◽  
pp. 165-172 ◽  
Author(s):  
Andrey K. Grishanin ◽  
Maxim V. Zagoskin
Keyword(s):  
Chromosome Number ◽  
Repetitive Sequences ◽  
Early Embryogenesis ◽  
Chromosome Size ◽  
Chromatin Diminution ◽  
Elimination Process ◽  
Dna Elimination ◽  
Molecular Studies ◽  
Cyclops Kolensis

Chromatin diminution (CD) is a phenomenon of programmed DNA elimination which takes place in early embryogenesis in some eukaryotes. The mechanism and biological role of CD remain largely unknown. During CD in the freshwater copepod Cyclops kolensis, the genome of cells of the somatic lineage is reorganized and reduced in size by more than 90% without affecting the genome of germline cells. Although the diploid chromosome number is unchanged, chromosome size is dramatically reduced by CD. The eliminated DNA consists primarily of repetitive sequences and localizes within granules during the elimination process. In this review, we provide an overview of CD in C. kolensis including both cytological and molecular studies.

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.

Can morphology and chromosome number contribute to species delimitation? A case in the Hibiscus trionum complex (Tribe Hibisceae, Malvaceae)

Phytotaxa ◽  
2019 ◽  
Vol 416 (4) ◽  
pp. 278-286
Author(s):  
MOHAMED OWIS BADRY ◽  
JENNIFER A. TATE ◽  
PRASHANT JOSHI ◽  
AHMED MAHMOUD ABBAS ◽  
SOHAIR THABET HAMED ◽  
...  
Keyword(s):  
Chromosome Number ◽  
Species Delimitation ◽  
Taxonomic Revision ◽  
Herbarium Specimens ◽  
Chromosome Counts ◽  
Comprehensive Description ◽  
Hibiscus Trionum ◽  
The World ◽  
First Time

A taxonomic revision of Hibiscus trionum from Egypt was undertaken using morphological and cytological studies of field collections and herbarium specimens. The data indicate that all specimens so far collected in Egypt belong to H. tridactylites, rather than H. trionum. This paper includes a comprehensive description of H. tridactylites, its occurrence, a comparison with other species in the H. trionum complex, and comments on habitat, along with images for easy identification. In addition, chromosome counts for this species from Egypt have been determined for the first time, which add to existing information on chromosome counts for the species from different regions of the world.

Cytology of somatic and gametangial nuclei in Phytophthora capsici and Phytophthora megasperma var. sojae

1974 ◽  
Vol 52 (9) ◽  
pp. 2055-2060 ◽  
Author(s):  
L. W. Stephenson ◽  
D. C. Erwin ◽  
J. V. Leary
Keyword(s):  
Chromosome Number ◽  
Chromosome Numbers ◽  
Phytophthora Capsici ◽  
Relative Size ◽  
Pollen Tubes ◽  
Reduction Division ◽  
Phytophthora Megasperma ◽  
Linear Alignment ◽  
Size Of Nuclei

Nuclear divisions in the hyphae and gametangia of Phytophthora capsici and in hyphae of Phytophthora megasperma var. sojae resembled those of typical mitosis. The chromosomal configurations in prophase are similar to classical angiosperm prophase configurations. However, in metaphase the linear alignment of chromosomes resembled the pattern reported in pollen tubes of Lilium and Tradescantia. The relative size of nuclei and numbers of chromosomes per nucleus remained constant during gametangial development. Somatic and gametangial nuclei were about equal in size and chromosome number. Chromosome numbers in somatic and gametangial nuclei of P. capsici and P. megasperma var. sojae were about six and eight, respectively. There was no evidence of reduction division in gametangia.

A contribution towards elucidating the life history of Palmaria palmate (=Rhodymenia palmata)

1976 ◽  
Vol 54 (24) ◽  
pp. 2903-2906 ◽  
Author(s):  
J. P. van der Meer
Keyword(s):  
Life History ◽  
Chromosome Number ◽  
Atlantic Coast ◽  
Palmaria Palmata ◽  
Haploid Chromosome Number ◽  
History Of

Palmaria palmata from a region of the Atlantic coast of Canada has been examined cytologically. Plants bearing tetrasporangia were found to be diploid with meiosis occurring in the tetrasporangia. Spermatangial plants and sporelings growing from tetraspores were haploid. The haploid chromosome number appears to be 22–23.

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