scholarly journals Morphology and Meiotic/Mitotic Behavior of B Cromosomes in a Japanese Harvestman, Metagagrella tenuipes (Arachnida: Opiliones): No Evidence for B Accumulation Mechanisms

2000 ◽  
Vol 17 (3) ◽  
pp. 349-355 ◽  
Author(s):  
Ivan P. Gorlov ◽  
Nobuo Tsurusaki
Keyword(s):  
Author(s):  
Т.В. Никитина ◽  
А.А. Кашеварова ◽  
М.М. Гридина ◽  
А.А. Хабарова ◽  
А.Г. Мензоров ◽  
...  

Митотическая нестабильность кольцевых хромосом может приводить к появлению клеточных клонов с различной генетической структурой. В качестве модели нестабильности кольцевых хромосом в митозе мы использовали фибробласты от пациентов с r(8), r(13), r(18) и r(22) и полученные из них индуцированные плюрипотентные стволовые клетки (ИПСК). Линии ИПСК с r(22) имели относительно стабильный кариотип на протяжении десятков (до 60) пассажей и сохраняли неизменную структуру кольцевой хромосомы. Кариотип линий ИПСК с r(8) и r(18) на ранних пассажах стабильный, планируется его изучение на поздних пассажах. Наибольшее разнообразие кариотипа выявлено в линиях ИПСК с r(13), в которых наблюдали различные перестройки и выраженную клеточную гетерогенность. Определение факторов, влияющих на митотическую стабильность кольцевых хромосом, может иметь значение для консультирования пациентов. Mitotic instability of ring chromosomes can lead to the appearance of cell clones with different genetic structure. IPSCs from fibroblasts of patients with r(8), r(13), r(18), and r(22) were used as a model of ring chromosomes mitotic behavior. Karyotypes of iPSC lines with r(8) and r(18) have so far been evaluated only in the early passages, lines with r(22) have maintained a relatively stable karyotype up to 60 passages. The occurrence of rearrangements and cellular heterogeneity was found characteristic for r(13) iPSCs. The determination of factors affecting the ring chromosomes mitotic stability would be beneficial for the patient’s prognosis.


2004 ◽  
Vol 19 (3) ◽  
pp. 274-279
Author(s):  
Shigeaki Kanatani ◽  
Hidenori Tabata ◽  
Kazunori Nakajima

Cortical formation in the developing brain is a highly complicated process involving neuronal production (through symmetric or asymmetric cell division) interaction of radial glia with neuronal migration, and multiple modes of neuronal migration. It has been convincingly demonstrated by numerous studies that radial glial cells are neural stem cells. However, the processes by which neurons arise from radial glia and migrate to their final destinations in vivo are not yet fully understood. Recent studies using time-lapse imaging of neuronal migration are giving investigators an increasingly more detailed understanding of the mitotic behavior of radial glia and the migrating behavior of their daughter cells. In this review, we describe recent progress in elucidating neuronal migration in brain formation and how neuronal migration is disturbed by mutations in genes that control this process. ( J Child Neurol 2005;20:274—279).


1996 ◽  
Vol 284 (2) ◽  
pp. 177-191 ◽  
Author(s):  
Volker C. Cordes ◽  
Sonja Reidenbach ◽  
Werner W. Franke

1959 ◽  
Vol 47 (5) ◽  
pp. 623-626 ◽  
Author(s):  
L. D. Liozner ◽  
Z. A. Ryabinina ◽  
V. F. Sidorova

1959 ◽  
Vol 37 (6) ◽  
pp. 1271-1276 ◽  
Author(s):  
Koichiro Tsunewaki

A plant having 41 normal rod-shaped chromosomes and a ring chromosome was found among hexaploid.F1 hybrids from a wheat–Agropyron cross. Cytological investigations were carried out to determine the mitotic behavior of this ring chromosome.The investigations revealed that most of the possible products of the breakage–fusion–bridge cycle known to occur in a ring chromosome were present in root tip cells. The fact that a rod-shaped chromosome is not derived from a ring chromosome in the cycle was confirmed, because no metaphase cells examined had 42 or more rod-shaped chromosomes.About 80% of the ring chromosomes were eliminated from the root tips of the seedling after 26 days. The size of the ring chromosome did not appear to influence the rate of elimination. The polyploid nature of the plant may account for the rapid, non-differential elimination of this chromosome.


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