DNA underreplication in intercalary heterochromatin regions in polytene chromosomes of Drosophila melanogaster correlates with the formation of partial chromosomal aberrations and ectopic pairing

Chromosoma ◽  
2006 ◽  
Vol 115 (5) ◽  
pp. 355-366 ◽  
Author(s):  
Elena S. Belyaeva ◽  
Sergey A. Demakov ◽  
Galina V. Pokholkova ◽  
Artyom A. Alekseyenko ◽  
Tatiana D. Kolesnikova ◽  
...  
1946 ◽  
Vol 62 (2) ◽  
pp. 114-119 ◽  
Author(s):  
B. M. Slizynski

The problem to be presented here emerges from the following groups of facts and more or less generally accepted opinions.As heterochromatin we may define those parts of chromosomes which reach maximum nucleic acid charge in mitosis or meiosis in times other than metaphase. In salivary gland chromosomes (which are more conveniently called polytene chromosomes) of Drosophila melanogaster the proximal heterochromatic parts of all chromosomes come together and form a central undifferentiated mass, the chromocentre. Genetically heterochromatin forms the so-called inert regions of the chromosomes.


Chromosoma ◽  
2003 ◽  
Vol 111 (6) ◽  
pp. 377-398 ◽  
Author(s):  
I. Zhimulev ◽  
E. Belyaeva ◽  
I. Makunin ◽  
V. Pirrotta ◽  
E. Volkova ◽  
...  

Chromosoma ◽  
2008 ◽  
Vol 117 (5) ◽  
pp. 411-418 ◽  
Author(s):  
E. S. Belyaeva ◽  
E. N. Andreyeva ◽  
S. N. Belyakin ◽  
E. I. Volkova ◽  
I. F. Zhimulev

Chromosoma ◽  
2009 ◽  
Vol 118 (6) ◽  
pp. 747-761 ◽  
Author(s):  
Natalya G. Andreyenkova ◽  
Elena B. Kokoza ◽  
Valery F. Semeshin ◽  
Elena S. Belyaeva ◽  
Sergey A. Demakov ◽  
...  

Chromosoma ◽  
1978 ◽  
Vol 70 (1) ◽  
pp. 1-17 ◽  
Author(s):  
E. V. Ananiev ◽  
V. A. Gvozdev ◽  
Yu. V. Ilyin ◽  
N. A. Tchurikov ◽  
G. P. Georgiev

2018 ◽  
Vol 479 (1) ◽  
pp. 114-117 ◽  
Author(s):  
V. A. Khoroshko ◽  
T. Yu. Zykova ◽  
O. O. Popova ◽  
I. F. Zhimulev

Genetics ◽  
2002 ◽  
Vol 161 (2) ◽  
pp. 733-746
Author(s):  
Jeffrey W Southworth ◽  
James A Kennison

Abstract The Sex combs reduced (Scr) gene specifies the identities of the labial and first thoracic segments in Drosophila melanogaster. In imaginal cells, some Scr mutations allow cis-regulatory elements on one chromosome to stimulate expression of the promoter on the homolog, a phenomenon that was named transvection by Ed Lewis in 1954. Transvection at the Scr gene is blocked by rearrangements that disrupt pairing, but is zeste independent. Silencing of the Scr gene in the second and third thoracic segments, which requires the Polycomb group proteins, is disrupted by most chromosomal aberrations within the Scr gene. Some chromosomal aberrations completely derepress Scr even in the presence of normal levels of all Polycomb group proteins. On the basis of the pattern of chromosomal aberrations that disrupt Scr gene silencing, we propose a model in which two cis-regulatory elements interact to stabilize silencing of any promoter or cis-regulatory element physically between them. This model also explains the anomalous behavior of the Scx allele of the flanking homeotic gene, Antennapedia. This allele, which is associated with an insertion near the Antennapedia P1 promoter, inactivates the Antennapedia P1 and P2 promoters in cis and derepresses the Scr promoters both in cis and on the homologous chromosome.


Genetics ◽  
1996 ◽  
Vol 144 (1) ◽  
pp. 197-204
Author(s):  
Christine Hoogland ◽  
Christian Biémont

Abstract Data of insertion site localization and site occupancy frequency of P, hobo, I, copia, mdg1, mdg3, 412, 297, and roo transposable elements (TEs) on the polytene chromosomes of Drosophila melanogaster were extracted from the literature. We show that TE insertion site number per chromosomal division was significantly correlated with the amount of DNA. The insertion site number weighted by DNA content was not correlated with recombination rate for all TEs except hobo, for which a positive correlation was detected. No global tendency emerged in the relationship between TE site occupancy frequency, weighted by DNA content, and recombination rate; a strong negative correlation was, however, found for the 3L arm. A possible dominant deleterious effect of chromosomal rearrangements due to recombination between TE insertions is thus not the main factor explaining the dynamics of TEs, since this hypothesis implies a negative relationship between recombination rate and both TE insertion site number and site occupancy frequency. The alternative hypothesis of selection against deleterious effects of insertional mutations is discussed.


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