Testis-specific expression and genomic multiplicity of the rat Rtdpoz genes that encode bipartite TRAF- and POZ/BTB-domain proteins

Gene ◽  
2007 ◽  
Vol 387 (1-2) ◽  
pp. 141-149 ◽  
Author(s):  
Kong-Bung Choo ◽  
Min-Chuan Hsu ◽  
Kowit-Yu Chong ◽  
Chiu-Jung Huang
2002 ◽  
Vol 116 (1-2) ◽  
pp. 217-221 ◽  
Author(s):  
Miwako Yamamoto ◽  
Yasuhisa Matsui

1999 ◽  
Vol 30 (10) ◽  
pp. 1201-1206 ◽  
Author(s):  
Peter Berger ◽  
Gerold Untergasser ◽  
Martin Hermann ◽  
Anton Hittmair ◽  
Stephan Madersbacher ◽  
...  

2019 ◽  
Vol 59 (4) ◽  
pp. 864-874 ◽  
Author(s):  
Justin C Havird ◽  
Hunter J McConie

Abstract Mitochondrial function is critical in eukaryotes. To maintain an adequate supply of energy, precise interactions must be maintained between nuclear- and mitochondrial-encoded gene products. Such interactions are paramount in chimeric enzymes such as the oxidative phosphorylation (OXPHOS) complexes. Mutualistic coevolution between the two genomes has therefore been suggested to be a critical, ubiquitous feature of eukaryotes that acts to maintain cellular function. However, mitochondrial genomes can also act selfishly and increase their own transmission at the expense of organismal function. For example, male-harming mutations are predisposed to accumulate in mitochondrial genomes due to their maternal inheritance (“mother’s curse”). Here, we investigate sexually antagonistic mitonuclear coevolution in nuclear-encoded OXPHOS paralogs from mammals and Drosophila. These duplicate genes are highly divergent but must interact with the same set of mitochondrial-encoded genes. Many such paralogs show testis-specific expression, prompting previous hypotheses suggesting they may have evolved under selection to counteract male-harming mitochondrial mutations. We found increased rates of evolution in OXPHOS paralogs with testis-specific expression in mammals and Drosophila, supporting this hypothesis. However, further analyses suggested such patterns may be due to relaxed, not positive selection, especially in Drosophila. Structural data also suggest that mitonuclear interactions do not play a major role in the evolution of many OXPHOS paralogs in a consistent way. In conclusion, no single OXPHOS paralog met all our criteria for being under selection to counteract male-harming mitochondrial mutations. We discuss alternative explanations for the drastic patterns of evolution in these genes, including mutualistic mitonuclear coevolution, adaptive subfunctionalization after gene duplication, and relaxed selection on OXPHOS in male tissues.


2014 ◽  
Vol 2014 ◽  
pp. 1-14 ◽  
Author(s):  
Daojun Cheng ◽  
Wenliang Qian ◽  
Meng Meng ◽  
Yonghu Wang ◽  
Jian Peng ◽  
...  

The BTB domain is a conserved protein-protein interaction motif. In this study, we identified 56 BTB domain-containing protein genes in the silkworm, in addition to 46 in the honey bee, 55 in the red flour beetle, and 53 in the monarch butterfly. Silkworm BTB protein genes were classified into nine subfamilies according to their domain architecture, and most of them could be mapped on the different chromosomes. Phylogenetic analysis suggests that silkworm BTB protein genes may have undergone a duplication event in three subfamilies: BTB-BACK-Kelch, BTB-BACK-PHR, and BTB-FLYWCH. Comparative analysis demonstrated that the orthologs of each of 13 BTB protein genes present a rigorous orthologous relationship in the silkworm and other surveyed insects, indicating conserved functions of these genes during insect evolution. Furthermore, several silkworm BTB protein genes exhibited sex-specific expression in larval tissues or at different stages during metamorphosis. These findings not only contribute to a better understanding of the evolution of insect BTB protein gene families but also provide a basis for further investigation of the functions of BTB protein genes in the silkworm.


PLoS ONE ◽  
2011 ◽  
Vol 6 (3) ◽  
pp. e17790 ◽  
Author(s):  
Christine K. Hamilton ◽  
Tamas Revay ◽  
Robin Domander ◽  
Laura A. Favetta ◽  
W. Allan King

2009 ◽  
Vol 15 (3) ◽  
pp. 165-171 ◽  
Author(s):  
K.M. Kusz ◽  
L. Tomczyk ◽  
M. Sajek ◽  
A. Spik ◽  
A. Latos-Bielenska ◽  
...  

Gene ◽  
2012 ◽  
Vol 499 (1) ◽  
pp. 143-153 ◽  
Author(s):  
Oxana M. Olenkina ◽  
Ksenia S. Egorova ◽  
Mikhail V. Kibanov ◽  
Yuri V. Gervaziev ◽  
Vladimir A. Gvozdev ◽  
...  

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