scholarly journals EFFICIENCIES OF GENES AND ACCURACY OF TREE-BUILDING METHODS IN RECOVERING A KNOWN DROSOPHILA GENEALOGY

2000 ◽  
Author(s):  
J. E. STEINBACHS ◽  
N. V. SCHIZAS ◽  
J. W. O. BALLARD
2011 ◽  
Vol 1 (7) ◽  
pp. 83-85
Author(s):  
Jasmine Jasmine ◽  
◽  
Pankaj Bhambri ◽  
Dr. O.P. Gupta Dr. O.P. Gupta

2009 ◽  
pp. 329-353 ◽  
Author(s):  
Manuel Gil ◽  
Gaston H. Gonnet

Genomics ◽  
2014 ◽  
Vol 104 (1) ◽  
pp. 1-7 ◽  
Author(s):  
William J. Faison ◽  
Alexandre Rostovtsev ◽  
Eduardo Castro-Nallar ◽  
Keith A. Crandall ◽  
Konstantin Chumakov ◽  
...  

1992 ◽  
Vol 70 (4) ◽  
pp. 715-723 ◽  
Author(s):  
J. J. Pasternak ◽  
B. R. Glick

The molecular evolution of the amino acid sequences of the mature small and large subunits of ribulose-1,5-bisphosphate carboxylase/oxygense (Rubisco) was determined. The dataset for each subunit consisted of sequences from 39 different taxa of which 22 are represented with sequence information for both subunits. Phylogenetic trees were reconstructed using distance matrix, parsimony and simultaneous alignment and phylogeny methods. For the small subunit, the latter two methods produced similar trees that differed from the topology of the distance matrix tree. For the large subunit, each of the three tree-building methods yielded a distinct tree. Except for the distance matrix small subunit tree, the tree-building methods produced topologies for the small and large subunit sequences from the nonflowering plant taxa that, for the most part, agree with current taxonomic schemes. With the full datasets, the lack of consistency both among the various trees and with conventional taxonomic relationships was most evident with the Rubisco sequences from angiosperms. It is unlikely that current tree-building methods will be able to reconstruct an unambiguous molecular evolution of either of the Rubisco subunits. Molecular trees, regardless of methodology, showed similar topologies for the small and large subunits from the 22 taxa from which both subunits have been sequenced, indicating that the subunits have changed to the same extent over time. In this case, similar trees were formed because only 4 of the 22 taxa were from dicots. Key words: ribulose-1,5-bisphosphate carboxylase/oxygenase, amino acid sequence, molecular evolution, phyletic trees.


2005 ◽  
Vol 360 (1462) ◽  
pp. 1905-1916 ◽  
Author(s):  
Rob DeSalle ◽  
Mary G Egan ◽  
Mark Siddall

Recent excitement over the development of an initiative to generate DNA sequences for all named species on the planet has in our opinion generated two major areas of contention as to how this ‘DNA barcoding’ initiative should proceed. It is critical that these two issues are clarified and resolved, before the use of DNA as a tool for taxonomy and species delimitation can be universalized. The first issue concerns how DNA data are to be used in the context of this initiative; this is the DNA barcode reader problem (or barcoder problem). Currently, many of the published studies under this initiative have used tree building methods and more precisely distance approaches to the construction of the trees that are used to place certain DNA sequences into a taxonomic context. The second problem involves the reaction of the taxonomic community to the directives of the ‘DNA barcoding’ initiative. This issue is extremely important in that the classical taxonomic approach and the DNA approach will need to be reconciled in order for the ‘DNA barcoding’ initiative to proceed with any kind of community acceptance. In fact, we feel that DNA barcoding is a misnomer. Our preference is for the title of the London meetings—Barcoding Life. In this paper we discuss these two concerns generated around the DNA barcoding initiative and attempt to present a phylogenetic systematic framework for an improved barcoder as well as a taxonomic framework for interweaving classical taxonomy with the goals of ‘DNA barcoding’.


2008 ◽  
Vol 48 (2) ◽  
pp. 563-573 ◽  
Author(s):  
Ana Sousa ◽  
Líbia Zé-Zé ◽  
Pedro Silva ◽  
Rogério Tenreiro

Parasitology ◽  
1999 ◽  
Vol 118 (6) ◽  
pp. 553-558 ◽  
Author(s):  
F. NILSEN

Small subunit (SSU) rDNA has been sequenced from a microsporidium, identified as a member of the genus Bacillidium obtained from an oligochaete. The length of the amplified PCR product was 1386 bp which is currently the longest microsporidium SSU sequence known. Phylogenetic analysis using 28 microsporidia SSU sequences, using 3 different tree-building methods indicated that Bacillidium sp. may be one of the earliest branches on the microsporidia tree. However, bootstrapping failed to give a high score (more than 50%) for the position of Bacillidium sp. The branch leading to Bacillidium sp. was long, indicating that this species is not closely related to any of the other microsporidia so far studied by means of rDNA.


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