Molecules match morphology: mitochondrial DNA supports Bayer's Lytreia - Bebryce - Heterogorgia (Alcyonacea : Octocorallia) clade hypothesis

2010 ◽  
Vol 24 (1) ◽  
pp. 23 ◽  
Author(s):  
Sergio Vargas ◽  
Michael Eitel ◽  
Odalisca Breedy ◽  
Bernd Schierwater

Several studies attempting to clarify the taxonomy and systematics of Octocorallia have highlighted the important role of molecular characters in corroborating or rejecting previous hypotheses based on morphological variation. One such hypothesis is that of a close phylogenetic relationship between the genera Lytreia, Bebryce and Heterogorgia proposed by Bayer based on morphological studies of the genera. Herein, we tested Bayer’s hypothesis using the mitochondrial marker mshI. We deduced a molecular phylogeny including members of the families Gorgoniidae and ‘Paramuriceidae’ that corroborated the existence of Bayer’s Lytreia–Bebryce–Heterogorgia clade. In addition, we provide a morphological assessment of the three genera as well as diagnoses for each of them. We also discuss, based on the phylogenetic results obtained, the evolution of sclerite morphology within Bayer’s Lytreia–Bebyce–Heterogorgia clade. Finally, we propose a Tethyan origin for the Lytreia–Bebryce–Heterogorgia clade.

2021 ◽  
Vol 7 (9) ◽  
pp. 136-143
Author(s):  
S. Rustamova ◽  
M. Ali

The review highlights animal coronaviruses, their pathogenicity, and the possible role of domestic and agricultural animals in the further spread of the COVID-19. Joint researches have been established amongst international team of scientists regarding a close phylogenetic relationship of the coronavirus SARS-CoV-2 with the coronaviruses of bats and carnivores, especially with the representatives of Felidae family (domestic cats). However, the case of Middle Eastern SARS transmitted by camels is required a special attention to biological safety measures in farms.


2008 ◽  
Vol 21 (2) ◽  
pp. 85-89
Author(s):  
Alicja Warowicka ◽  
Joanna Pacholska-Bogalska ◽  
Anna Kwaśniewska ◽  
Anna Goździcka-Józefiak
Keyword(s):  

2021 ◽  
pp. 1485-1499
Author(s):  
Ryan J. Snyder ◽  
Steven R. Kleeberger

Genetics ◽  
1997 ◽  
Vol 145 (3) ◽  
pp. 697-705 ◽  
Author(s):  
Philippe Silar ◽  
France Koll ◽  
Michèle Rossignol

The filamentous fungus Podospora anserina presents a degeneration syndrome called Senescence associated with mitochondrial DNA modifications. We show that mutations affecting the two different and interacting cytosolic ribosomal proteins (S7 and S19) systematically and specifically prevent the accumulation of senDNAα (a circular double-stranded DNA plasmid derived from the first intron of the mitochondrial cox1 gene or intron α) without abolishing Senescence nor affecting the accumulation of other usually observed mitochondrial DNA rearrangements. One of the mutant proteins is homologous to the Escherichia coli S4 and Saccharomyces cerevisiae S13 ribosomal proteins, known to be involved in accuracy control of cytosolic translation. The lack of accumulation of senDNAα seems to result from a nontrivial ribosomal alteration unrelated to accuracy control, indicating that S7 and S19 proteins have an additional function. The results strongly suggest that modified expression of nucleus-encoded proteins contributes to Senescence in P. anserina. These data do not fit well with some current models, which propose that intron α plays the role of the cytoplasmic and infectious Determinant of Senescence that was defined in early studies.


2021 ◽  
Vol 22 (10) ◽  
pp. 5100
Author(s):  
Paulina Kozakiewicz ◽  
Ludmiła Grzybowska-Szatkowska ◽  
Marzanna Ciesielka ◽  
Jolanta Rzymowska

The mitochondria are essential for normal cell functioning. Changes in mitochondrial DNA (mtDNA) may affect the occurrence of some chronic diseases and cancer. This process is complex and not entirely understood. The assignment to a particular mitochondrial haplogroup may be a factor that either contributes to cancer development or reduces its likelihood. Mutations in mtDNA occurring via an increase in reactive oxygen species may favour the occurrence of further changes both in mitochondrial and nuclear DNA. Mitochondrial DNA mutations in postmitotic cells are not inherited, but may play a role both in initiation and progression of cancer. One of the first discovered polymorphisms associated with cancer was in the gene NADH-ubiquinone oxidoreductase chain 3 (mt-ND3) and it was typical of haplogroup N. In prostate cancer, these mutations and polymorphisms involve a gene encoding subunit I of respiratory complex IV cytochrome c oxidase subunit 1 gene (COI). At present, a growing number of studies also address the impact of mtDNA polymorphisms on prognosis in cancer patients. Some of the mitochondrial DNA polymorphisms occur in both chronic disease and cancer, for instance polymorphism G5913A characteristic of prostate cancer and hypertension.


2007 ◽  
Vol 27 (3) ◽  
pp. 370-377 ◽  
Author(s):  
Shankai Yin ◽  
Zhiping Yu ◽  
Ravi Sockalingam ◽  
Manohar Bance ◽  
Genlou Sun ◽  
...  

1970 ◽  
Vol 12 (4) ◽  
pp. 790-794 ◽  
Author(s):  
Chi-Chang Chen ◽  
Pryce B. Gibson

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.


Mitochondrion ◽  
2002 ◽  
Vol 2 (1-2) ◽  
pp. 27-37 ◽  
Author(s):  
Giuseppe Attardi

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