chromosomal homology
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The Nucleus ◽  
2021 ◽  
Author(s):  
Weera Thongnetr ◽  
Wiwat Sangpakdee ◽  
Alongklod Tanomtong ◽  
Wenhui Nie ◽  
Sayam Raso ◽  
...  


2013 ◽  
Vol 7 (1) ◽  
pp. 11-23 ◽  
Author(s):  
Venu Govindappa ◽  
G Venkatachalaiah
Keyword(s):  


2010 ◽  
Vol 38 (15) ◽  
pp. e152-e152 ◽  
Author(s):  
Salvatore J. Orlando ◽  
Yolanda Santiago ◽  
Russell C. DeKelver ◽  
Yevgeniy Freyvert ◽  
Elizabeth A. Boydston ◽  
...  


2008 ◽  
Vol 57 (1) ◽  
pp. 29-32
Author(s):  
Anna Bratuś ◽  
Monika Bugno ◽  
Jolanta Klukowska-Rötzler ◽  
Małgorzata Sawińska ◽  
Andre Eggen ◽  
...  


2004 ◽  
Vol 21 (8) ◽  
pp. 1339-1348 ◽  
Author(s):  
S. E. Hampson ◽  
B. S. Gaut ◽  
P. Baldi


Genetics ◽  
1999 ◽  
Vol 151 (1) ◽  
pp. 151-161 ◽  
Author(s):  
Sigrid Steinemann ◽  
Manfred Steinemann

Abstract On the basis of chromosomal homology, the Amylase gene cluster in Drosophila miranda must be located on the secondary sex chromosome pair, neo-X (X2) and neo-Y, but is autosomally inherited in all other Drosophila species. Genetic evidence indicates no active amylase on the neo-Y chromosome and the X2-chromosomal locus already shows dosage compensation. Several lines of evidence strongly suggest that the Amy gene cluster has been lost already from the evolving neo-Y chromosome. This finding shows that a relatively new neo-Y chromosome can start to lose genes and hence gradually lose homology with the neo-X. The X2-chromosomal Amy1 is intact and Amy2 contains a complete coding sequence, but has a deletion in the 3′-flanking region. Amy3 is structurally eroded and hampered by missing regulatory motifs. Functional analysis of the X2-chromosomal Amy1 and Amy2 regions from D. miranda in transgenic D. melanogaster flies reveals ectopic AMY1 expression. AMY1 shows the same electrophoretic mobility as the single amylase band in D. miranda, while ectopic AMY2 expression is characterized by a different mobility. Therefore, only the Amy1 gene of the resident Amy cluster remains functional and hence Amy1 is the dosage compensated gene.



Genome ◽  
1998 ◽  
Vol 41 (4) ◽  
pp. 510-526 ◽  
Author(s):  
J T Zhao ◽  
M Frommer ◽  
J A Sved ◽  
A Zacharopoulou

The Queensland fruit fly, Bactrocera tryoni, like the Mediterranean fruit fly, Ceratitis capitata, has a diploid complement of 12 chromosomes, including five pairs of autosomes and a XX/XY sex chromosome pair. Characteristic features of each chromosome are described. Chromosomal homology between B. tryoni and C. capitata has been determined by comparing chromosome banding pattern and in situ hybridisation of cloned genes to polytene chromosomes. Although the evidence indicates that a number of chromosomal inversions have occurred since the separation of the two species, synteny of the chromosomes appears to have been maintained.Key words: tephritid fruit fly, Bactrocera tryoni, polytene chromosomes, in situ hybridisation, chromosomal homology.



1995 ◽  
Vol 176 (2) ◽  
pp. 247-260 ◽  
Author(s):  
Dietmar Dorninger ◽  
Günther Karigl ◽  
Josef Loidl


1982 ◽  
Vol 38 (12) ◽  
pp. 1485-1487 ◽  
Author(s):  
M. H. Gallardo
Keyword(s):  


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