RFLP analysis of a mitochondrial gene, cytochrome oxidase I (COI) of three species of the genusCalyptogena around Japan

1995 ◽  
Vol 51 (2) ◽  
pp. 257-259 ◽  
Author(s):  
Shigeaki Kojima ◽  
Takanori Kobayashi ◽  
Jun Hashimoto ◽  
Suguru Ohta
1995 ◽  
Vol 308 (2) ◽  
pp. 665-671 ◽  
Author(s):  
T P Mayall ◽  
I Bjarnason ◽  
U Y Khoo ◽  
T J Peters ◽  
A J S Macpherson

Most mitochondrial genes are transcribed as a single large transcript from the heavy strand of mitochondrial DNA, and are subsequently processed into the proximal mitochondrial (mt) 12 S and 16 S rRNAs, and the more distal tRNAs and mRNAs. We have shown that in intestinal epithelial biopsies the steady-state levels of mt 12 S and 16 S rRNA are an order of magnitude greater than those of mt mRNAs. Fractionation of rat small intestinal epithelial cells on the basis of their maturity has shown that the greatest ratios of 12 S mt rRNA/cytochrome b mt mRNA or 12 S mt rRNA/cytochrome oxidase I mt mRNA are found in the surface mature enterocytes, with a progressive decrease towards the crypt immature enteroblasts. Cytochrome b and cytochrome oxidase I mt mRNA levels are relatively uniform along the crypt-villus axis, but fractionation experiments showed increased levels in the crypt base. The levels of human mitochondrial transcription factor A are also greater in immature crypt enteroblasts compared with mature villus enterocytes. These results show that the relative levels of mt rRNA and mRNA are distinctly regulated in intestinal epithelial cells according to the crypt-villus position and differentiation status of the cells, and that there are higher mt mRNA and mt TFA levels in the crypts, consistent with increased transcriptional activity during mitochondrial biogenesis in the immature enteroblasts.


Zootaxa ◽  
2011 ◽  
Vol 3007 (1) ◽  
pp. 50
Author(s):  
KATHRYN M. WEGLARZ ◽  
CHARLES R. BARTLETT

The new delphacid genus Akemetopon gen. n. (Delphacinae: Delphacini) is described and illustrated with 3 new species from Arizona and Mexico: Akemetopon inornatum sp. n., A. politum sp. n., and A. ainigma sp. n. A key to species is provided. The barcoding portion of the mitochondrial gene Cytochrome Oxidase I (COI) was sequenced for A. politum sp. n. A maximum likelihood analysis places this genus in the basal Delphacini.


Zootaxa ◽  
2006 ◽  
Vol 1363 (1) ◽  
pp. 49 ◽  
Author(s):  
CATHERINE N. DUCKETT ◽  
K. D. PRATHAPAN ◽  
ALEXANDER S. KONSTANTINOV

Genus Ivalia Jacoby is characterized morphologically, and Amphimeloides Jacoby syn. nov. and Taizonia Chen syn. nov. are junior synonyms with it. Several Ivalia species are figured, including Ivalia bella (Chen) comb. nov., I. dorsalis (Jacoby) comb. nov., and I. viridipennis Jacoby. A new species of Ivalia from the Nilgiri Hills in south India, I. korakundah sp. nov., is described and illustrated, including the larvae. Larvae were associated with adults by sequencing a fragment of the mitochondrial gene cytochrome oxidase I. Larval morphology is discussed and compared with that of other flea beetles.


2015 ◽  
Vol 63 (2) ◽  
pp. 369 ◽  
Author(s):  
Cedar I. García-Ríos

<p>The genus <em>Lepidochitona</em> (Gray 1821) contains relatively small chitons with a distinctive girdle, dorsally clothed with non-overlapping calcareous corpuscles. In the Caribbean, it is represented by four species: <em>L. liozonis</em> (Dall, &amp; Simpson, 1901), <em>L. rosea</em> Kaas, 1972, <em>L. rufoi</em> García-Ríos, 2010 and <em>L. bullocki</em> García-Ríos, 2011. A rutinary morphological inspection of 10 specimens of a <em>Lepidochitona</em> species from the Florida Keys was concordant with <em>L. liozonis </em>(the only species of the genus informed for Florida). They did not show many morphological differences that could justify its separation from the specimens from Puerto Rico (the type locality). However, the comparison of sequences of the mitochondrial gene coding for cytochrome oxidase I (COI) of <em>L. liozonis </em>from Puerto Rico and the Florida specimens showed a divergence of 14%. This divergence is incompatible with a reproductively connected species. In addition to their genetic differences, the new species differs from <em>L</em>. <em>liozonis</em> in having bigger size, longer marginal spicules and a postmucronal slope very concave.</p>


2011 ◽  
Vol 6 (1) ◽  
pp. 56 ◽  
Author(s):  
Eric Faure ◽  
Luis Delaye ◽  
Sandra Tribolo ◽  
Anthony Levasseur ◽  
Hervé Seligmann ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document