scholarly journals Rapid evolution of the compact and unusual mitochondrial genome in the ctenophore, Pleurobrachia bachei

2012 ◽  
Vol 63 (1) ◽  
pp. 203-207 ◽  
Author(s):  
Andrea B. Kohn ◽  
Mathew R. Citarella ◽  
Kevin M. Kocot ◽  
Yelena V. Bobkova ◽  
Kenneth M. Halanych ◽  
...  
2018 ◽  
Author(s):  
Andrea B. Kohn ◽  
Leonid L. Moroz

AbstractThe mitochondrial genomes in ctenophores are among the most compact in the animal kingdom with multiple rearrangements and examples of gene loss. Here, by resequencing of the Pleurobrachia bachei mitochondrial genome, we show that the high level of polymorphism (>10%) in Pleurobrachia might contribute to the ongoing fast evolution of ctenophores including the presence of truncated versions of apparently canonical genes such as cox1. Second, the codon interpretations in ctenophores, without robust proteomic data related to mitochondrial genes, is still a challenging issue, which is open for future experimental analyses.


The mitochondrial genomes of higher plants are among the largest and most complex organelle genomes described. They are generally multicircular or partly linear; in some species, extrachromosomal plasmids are present. It is proposed that inter- and intramolecular homologous recombination can account for the diversity of the observed genome organizations. The ability of mitochondria to fuse establishes a panmictic mitochondrial DNA population which is in recombinational equilibrium. It is suggested that this suppresses the base mutation rate, and unequal partitioning of the cytoplasm during cell division can lead to the rapid evolution of mitochondrial genome structure. This contrasts with the observed rates of base-sequence and genome evolution in chloroplasts. This difference can be accounted for solely by the inability of chloroplasts to fuse, thereby preventing chloroplast genome panmixis.


PLoS ONE ◽  
2011 ◽  
Vol 6 (11) ◽  
pp. e26645 ◽  
Author(s):  
Jin-Hua Xiao ◽  
Jing-Guo Jia ◽  
Robert W. Murphy ◽  
Da-Wei Huang

Swiss Surgery ◽  
1999 ◽  
Vol 5 (3) ◽  
pp. 143-146 ◽  
Author(s):  
Launois ◽  
Maddern ◽  
Tay

The detailed knowledge of the segmental anatomy of the liver has led to a rapid evolution in resectional surgery based on the intrahepatic distribution of the portal trinity (the hepatic artery, hepatic duct and portal vein). The classical intrafascial or extrahepatic approach is to isolate the appropriate branch of the portal vein, hepatic artery and the hepatic duct, outside the liver substance. Another method, the extrafascial approach, is to dissect the whole sheath of the pedicle directly after division of a substantial amount of the hepatic tissue to reach the pedicle, which is surrounded by a sheath, derived from Glisson's capsule. This Glissonian sheath encloses the portal trinity. In the transfissural or intrahepatic approach, these sheaths can be approached either anteriorly (after division of the main, right or umbilical fissure) or posteriorly from behind the porta hepatis. We describe the technique for approaching the Glissonian sheath and hence the hepatic pedicle structures and their branches by the intrahepatic posterior approach that allows early delineation of the liver segment without the need for ancillary techniques. In addition, the indications for the use of this technique in the technical and oncologic settings are also discussed.


2018 ◽  
Vol XIII (3) ◽  
Author(s):  
I.О. Маzunin

Psihiatru ro ◽  
2019 ◽  
Vol 58 (3) (1) ◽  
pp. 18-20
Author(s):  
Cătălina Crişan ◽  
Laura Grosu ◽  
Oana Vanţa

Gayet-Wernicke encephalopathy is an acute neuropsychiatric condition caused by thiamine deficiency. Only a small percentage of patients experience all three symptoms, with ophtalmoplegia, ataxia and confusion, and the full triad occurs more frequently among those who have overused alcohol. The evolution is toward full recovery, Korsakoff syndrome, dementia or death. We present the case of a 56-year-old patient, known with a diagnostic of alcoholism, who was admitted for a complicated withdrawal syndrome with delirium and who developed encephalopathy and dementia syndrome.


Sign in / Sign up

Export Citation Format

Share Document