scholarly journals Effect of egg turning and incubation time on carbonic anhydrase gene expression in the blastoderm of the Japanese quail (Coturnix c. japonica)

2008 ◽  
Vol 49 (5) ◽  
pp. 566-573 ◽  
Author(s):  
P. De Winter ◽  
D. Sugden ◽  
G.K. Baggott
2019 ◽  
Vol 201 (22) ◽  
Author(s):  
Lydia M. Varesio ◽  
Jonathan W. Willett ◽  
Aretha Fiebig ◽  
Sean Crosson

ABSTRACT Brucella spp. are intracellular pathogens that cause a disease known as brucellosis. Though the genus is highly monomorphic at the genetic level, species have animal host preferences and some defining physiologic characteristics. Of note is the requirement for CO2 supplementation to cultivate particular species, which confounded early efforts to isolate B. abortus from diseased cattle. Differences in the capacity of Brucella species to assimilate CO2 are determined by mutations in the carbonic anhydrase gene, bcaA. Ancestral single-nucleotide insertions in bcaA have resulted in frameshifted pseudogenes in B. abortus and B. ovis lineages, which underlie their inability to grow under the low CO2 tension of a standard atmosphere. Incubation of wild-type B. ovis in air selects for mutations that “rescue” a functional bcaA reading frame, which enables growth under low CO2 and enhances the growth rate under high CO2. Accordingly, we show that heterologous expression of functional Escherichia coli carbonic anhydrases enables B. ovis growth in air. Growth of B. ovis is acutely sensitive to a reduction in CO2 tension, while frame-rescued B. ovis mutants are insensitive to CO2 shifts. B. ovis initiates a gene expression program upon CO2 downshift that resembles the stringent response and results in transcriptional activation of its type IV secretion system. Our study provides evidence that loss-of-function insertion mutations in bcaA sensitize the response of B. ovis and B. abortus to reduced CO2 tension relative to that of other Brucella lineages. CO2-dependent starvation and virulence gene expression programs in these species may influence persistence or transmission in natural hosts. IMPORTANCE Brucella spp. are highly related, but they exhibit differences in animal host preference that must be determined by genome sequence differences. B. ovis and the majority of B. abortus strains require high CO2 tension to be cultivated in vitro and harbor conserved insertional mutations in the carbonic anhydrase gene, bcaA, which underlie this trait. Mutants that grow in a standard atmosphere, first reported nearly a century ago, are easily selected in the laboratory. These mutants harbor varied indel polymorphisms in bcaA that restore its consensus reading frame and rescue its function. Loss of bcaA function has evolved independently in the B. ovis and B. abortus lineages and results in a dramatically increased sensitivity to CO2 limitation.


2006 ◽  
Vol 571 (2) ◽  
pp. 319-327 ◽  
Author(s):  
Peiwen Pan ◽  
Mari Leppilampi ◽  
Silvia Pastorekova ◽  
Jaromir Pastorek ◽  
Abdul Waheed ◽  
...  

1991 ◽  
Vol 39 (4) ◽  
pp. 451-459 ◽  
Author(s):  
H K Väänänen ◽  
N D Carter ◽  
S J Dodgson

We used a monospecific polyclonal antiserum against mitochondrial carbonic anhydrase (CA V) from rat liver to study tissue localization of this new member of the carbonic anhydrase gene family. Strong granular immunostaining reaction of CA V was observed in hepatocytes, myocardium, and in certain populations of skeletal muscle fibers. This is the first time that mitochondrial carbonic anhydrase is described in cardiac tissue of rat or any other species. Different epithelial cells revealed very heterogeneous staining reaction, suggesting that mitochondria are a heterogeneous population with respect to their CA V content. Many cells in different glandular epithelia did not show any CA V, whereas some cells, such as gastric parietal cells, were intensely stained with CA V antibodies. No systematic co-expression of CA V with CA I, CA II, or CA III was observed, although the distribution of CA V in skeletal muscle was somewhat similar to that of CA III. Connective tissue cells such as fibroblasts, chondroblasts, and osteoblasts were negative.


2011 ◽  
Vol 25 (S1) ◽  
Author(s):  
JongJoo Lee ◽  
Sang‐Hyun Song ◽  
Ann Dean

1996 ◽  
Vol 65 (1) ◽  
pp. 51-56
Author(s):  
O. M. Andrisani ◽  
A. R. Irizarry ◽  
S. K. Wolfe ◽  
J. C. Vellinger ◽  
R. L. Hullinger

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