scholarly journals ICSI with All Oocytes Recurrent Metaphase I Characterized by Absence Perivitelline Space

2021 ◽  
Vol 11 (09) ◽  
pp. 1112-1116
Author(s):  
Yan Jiang ◽  
Ge Song ◽  
Jingchuan Yuan ◽  
Xuhui Zhang
Keyword(s):  
Perivitelline Space ◽  
Metaphase I

Protein Synthesis Controls Cyclin Stability in Metaphase I-Arrested Oocytes of Patella vulgata

1993 ◽  
Vol 208 (2) ◽  
pp. 518-521 ◽  
Author(s):  
Pierre Colas ◽  
Catherine Launay ◽  
André E. van Loon ◽  
Pierre Guerrier
Keyword(s):  
Protein Synthesis ◽  
Patella Vulgata ◽  
Metaphase I

CYTOLOGICAL STUDIES ON THE ORIGIN OF JOHNSON GRASS

1969 ◽  
Vol 11 (1) ◽  
pp. 25-29 ◽  
Author(s):  
Samir P. Mouftah ◽  
J. D. Smith
Keyword(s):  
Statistical Analysis ◽  
Sorghum Vulgare ◽  
Johnson Grass ◽  
Species Hybrids ◽  
Advanced Generation ◽  
Metaphase I

Observations were made at diakinesis and metaphase I of the frequencies of the various types of chromosomal associations in advanced generation allotetraploids of Sorghum vulgare × S. virgatum and in tri-species hybrids of (S. vulgare × S. virgatum)2 × S. halepense. The most frequent configurations were bivalents and quadrivalents, although all combinations from univalent to hexavalent were seen. Statistical analysis of the data failed to differentiate between the chomosomal behavior of the allotetraploids and that of the tri-species hybrids. This supports the hypothesis that S. vulgare and S. virgatum are the diploid progenitors of S. halepense.

RELATIONSHIP OF TAXA IN GENUS MEDICAGO AS REVEALED BY HYBRIDIZATION.: II. M. PIRONAE × M. DAGHESTANICA WITH REFERENCE TO M. SATIVA

1968 ◽  
Vol 10 (2) ◽  
pp. 454-459 ◽  
Author(s):  
K. Lesins ◽  
C. B. Gillies
Keyword(s):  
The Past ◽  
Relationship Of ◽  
Chromatin Bridges ◽  
Metaphase I

Medicago pironae Vis. and M. daghestanica Rupr. are related to the extent that viable F1 hybrids can be easily obtained. These species should, therefore, be grouped taxonomically closer than has been done in the past. Their relationship to M. sativa L. is more remote, as judged by failure in hybridization. The M. pironae × M. daghestanica F1 hybrids were completely self-sterile and sterile on backcrossing to both parents. Pollen of the hybrids was close to 100% protoplasm-empty. Meiosis proceeded irregularly in 55% of metaphase I and diakinesis cells. At AI and All chromatin bridges were observed in 65% and 90% of cells, respectively. At pachytene, strands of unequal lengths and different chromomere patterns indicated cryptic chromosomal or genie dissimilarities.

CHROMOSOME PAIRING IN TWO INTERSPECIFIC HYBRIDS OF TRIFOLIUM

1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson
Keyword(s):  
Phylogenetic Relationship ◽  
Chromosome Pairing ◽  
Trifolium Repens ◽  
Interspecific Hybrids ◽  
Triploid Hybrid ◽  
Close Phylogenetic Relationship ◽  
Metaphase I

Both Trifolium repens (2n = 32) and T. nigrescens (2n = 16) formed bivalents during meiosis. However, their triploid hybrid showed an average of 4.27 trivalents per microsporocyte at metaphase I. The frequency of trivalents in the hybrid between T. nigrescens and autotetraploid T. occidentale (2n = 32) was 5.69. The data are interpreted to indicate: (1) a possible autotetraploid origin of T. repens; and (2) a close phylogenetic relationship among T. repens, T. nigrescens and T. occidentale.

Rye C-banding patterns and meiotic stability of hexaploid triticale (× Triticosecale) selections differing in kernel shriveling

Genome ◽  
1990 ◽  
Vol 33 (5) ◽  
pp. 686-689 ◽  
Author(s):  
Charles M. Papa ◽  
R. Morris ◽  
J. W. Schmidt
Keyword(s):  
Secale Cereale ◽  
Chromosome Banding ◽  
Agronomic Performance ◽  
Hexaploid Triticale ◽  
Kernel Development ◽  
Banding Patterns ◽  
C Banding ◽  
Meiotic Stability ◽  
Metaphase I

Two winter hexaploid triticale populations derived from the same cross were selected on the basis of grain appearance and agronomic performance. The five lines from 84LT402 showed more kernel shriveling than the four lines from 84LT401. The derived lines were analyzed for aneuploid frequencies, rye chromosome banding patterns, and meiotic stability to detect associations with kernel development. The aneuploid frequencies were 16% in 84LT401 and 18% in 84LT402. C-banding showed that both selection groups had all the rye chromosomes except 2R. The two groups had similar telomeric patterns but differed in the long-arm interstitial patterns of 4R and 5R. Compared with lines from 84LT402, those from 84LT401 had significantly fewer univalents and rod bivalents, and more paired arms at metaphase I; fewer laggards and bridges at anaphase I; and a higher frequency of normal tetrads. There were no significant differences among lines within each group for any meiotic character. Since there were no differences within or between groups in telomeric banding patterns, the differences in kernel shriveling and meiotic stability might be due to genotypic factors and (or) differences in the interstitial patterns of 4R and 5R. By selecting plump grains, lines with improved kernel characteristics along with improved meiotic stability are obtainable.Key words: triticale, meiotic stability, C-banding, Secale cereale, heterochromatin.

Synaptonemal complex proteins: occurrence, epitope mapping and chromosome disjunction

1994 ◽  
Vol 107 (10) ◽  
pp. 2749-2760 ◽  
Author(s):  
M.J. Dobson ◽  
R.E. Pearlman ◽  
A. Karaiskakis ◽  
B. Spyropoulos ◽  
P.B. Moens
Keyword(s):  
Synaptonemal Complex ◽  
Fusion Proteins ◽  
Epitope Mapping ◽  
Core Protein ◽  
Binding Capacity ◽  
Polyclonal Antibodies ◽  
Meiotic Chromosome ◽  
Immunogold Labelling ◽  
Chromosome Disjunction ◽  
Metaphase I

We have used polyclonal antibodies against fusion proteins produced from cDNA fragments of a meiotic chromosome core protein, Cor1, and a protein present only in the synapsed portions of the cores, Syn1, to detect the occurrence and the locations of these proteins in rodent meiotic prophase chromosomes. The 234 amino acid Cor1 protein is present in early unpaired cores, in the lateral domains of the synaptonemal complex and in the chromosome cores when they separate at diplotene. A novel observation showed the presence of Cor1 axial to the metaphase I chromosomes and substantial amounts of Cor1 in association with pairs of sister centromeres. The centromere-associated Cor1 protein becomes dissociated from the centromeres at anaphase II and it is not found in mitotic metaphase centromeres. The extended presence of Cor1 suggests that it may have a role in chromosome disjunction by fastening chiasmata at metaphase I and by joining sister kinetochores, which ensures co-segregation at anaphase I. Two-colour immunofluorescence of Cor1 and Syn1 demonstrates that synapsis between homologous cores is initiated at few sites but advances rapidly relative to the establishment of new initiation sites. If the rapid advance of synapsis deters additional initiation sites between pairs of homologues, it may provide a mechanism for positive recombination interference. Immunogold epitope mapping of antibodies to four Syn1 fusion proteins places the amino terminus of Syn1 towards the centre of the synaptonemal complex while the carboxyl terminus extends well into the lateral domain of the synaptonemal complex. The Syn1 fusion proteins have a non-specific DNA binding capacity. Immunogold labelling of Cor1 antigens indicates that the lateral domain of the synaptonemal complex is about twice as wide as the apparent width of lateral elements when stained with electron-dense metal ions. Electron microscopy of shadow-cast surface-spread SCs confirms the greater width of the lateral domain. The implication of these dimensions is that the proteins that comprise the synaptic domain overlap with the protein constituents of the lateral domains of the synaptonemal complex more than was apparent from earlier observations. This arrangement suggests that direct interactions might be expected between some of the synaptonemal complex proteins.

Analysis of the mechanism(s) of metaphase I arrest in strain LT mouse oocytes: participation of MOS

Development ◽  
1997 ◽  
Vol 124 (24) ◽  
pp. 5107-5113
Author(s):  
Y. Hirao ◽  
J.J. Eppig
Keyword(s):  
Potential Role ◽  
Inbred Strains ◽  
Mitogen Activated Protein Kinase ◽  
Null Mutation ◽  
Mitogen Activated Protein ◽  
Cytostatic Factor ◽  
Almost All ◽  
Dependent Mechanism ◽  
Metaphase I

Oocytes of almost all vertebrates become arrested at metaphase II to await fertilization. Arrest is achieved with the participation of a protein complex known as cytostatic factor (CSF) that stabilizes histone H1 kinase activity. MOS and mitogen-activated protein kinase (MAPK) are important components of CSF. Strain LT/Sv mice, and strains related to LT/Sv, produce a high percentage of atypical oocytes that are arrested at metaphase I when normal oocytes have progressed to metaphase II. The potential role of MOS in metaphase I arrest was investigated using strain LT/Sv and LT-related recombinant inbred strains, LTXBO and CX8-4. MOS and MAPK are produced and functional in maturing LT oocytes. Two experimental paradigms were used to reduce or delete MOS in LT oocytes and assess effects on metaphase I arrest. First, sense and antisense Mos oligonucleotides were microinjected into metaphase I-arrested oocytes. Antisense, but not sense, Mos oligonucleotides promoted the activation of metaphase I-arrested oocytes. Second, mice carrying a Mos null mutation were crossed with LT mice, the null mutation was backcrossed three times to LT mice, and Mos(+/−) N3 mice were intercrossed to produce Mos(−/−), Mos(+/−) and Mos(+/+) N3F1 mice. Oocytes of all three Mos genotypes of N3F1 mice sustained meiotic arrest for 17 hours indicating that metaphase I arrest is not initiated by a MOS-dependent mechanism. However, unlike Mos(+/+) and Mos(+/−) CX8-4 N3F1 oocytes, metaphase I arrest of Mos(−/−) CX8-4 N3F1 oocytes was not sustained after 17 hours and became reversed gradually. These results, like the antisense Mos oligonucleotide microinjection experiments, suggest that MOS participates in sustaining metaphase I arrest in LT oocytes.

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