scholarly journals Analysis of chloroplast ribosomal subunit S16 (rpS16) intron sequences in Morus (Urticales: Moraceae)

2011 ◽  
Vol 10 (77) ◽  
Author(s):  
Wang Yuhua
Phytotaxa ◽  
2019 ◽  
Vol 427 (1) ◽  
pp. 43-50 ◽  
Author(s):  
LONG WANG ◽  
QIAN XING ◽  
GENG-YU LU ◽  
XU LU ◽  
QUN ZHAO ◽  
...  

Amana baohuaensis is described and illustrated as a new species from Jurong City, Jiangsu Province, East China. The new species is morphologically similar to A. edulis, but differs from the latter by having three verticillate linear bracts, white or purple-red solitary flowers, and purplish-brown anthers. Phylogenetic analyses based on nuclear ITS, chloroplast matK and rps16 intron sequences confirmed that this new species is distinct from morphologically similar species.


2009 ◽  
Vol 43 (1) ◽  
pp. 32-38 ◽  
Author(s):  
E. V. Martirosyan ◽  
N. N. Ryzhova ◽  
E. Z. Kochieva ◽  
K. G. Skryabin

1999 ◽  
Vol 77 (8) ◽  
pp. 1120-1135 ◽  
Author(s):  
Stephen R Downie ◽  
Deborah S Katz-Downie

Evolutionary relationships among 48 genera of Apiaceae (Umbelliferae) were inferred using maximum parsimony, maximum-likelihood, and neighbor-joining analyses of chloroplast DNA rps16 intron and adjacent rps16 3prime exon sequences. Emphasis was placed on woody members of Apiaceae subfamily Apioideae endemic to southern Africa, a region hypothesized to be the place of origin of this largely herbaceous subfamily. The resultant phylogenies were highly concordant and indicate that the apioid genera Polemanniopsis and Steganotaenia form a clade sister to Apiaceae subfamily Saniculoideae. The African genera Anginon, Dracosciadium, Glia, Heteromorpha, and Polemannia also comprise a clade and likely represent the most basal elements within Apioideae. Heteromorpha, however, is not monophyletic, with Heteromorpha arborescens (Spreng.) Cham. & Schltdl. var. abyssinica (A. Rich.) H. Wolff and Heteromorpha arborescens (Spreng.) Cham. & Schltdl. var. arborescens arising in separate subclades. Progressing up the trees, Annesorhiza then Bupleurum fall as successive sister taxa to all remaining Apioideae. The major clades recognized within subfamily Apioideae are largely congruent with those inferred using other types of molecular evidence. Sequence divergence is similar to that of other chloroplast introns, including being generally low among congeners and woody taxa. While the rps16 intron has seen very little use in molecular systematic studies to date, this study demonstrates its ability to discern high-level relationships within Apiaceae.Key words: Apiaceae, Apioideae, chloroplast rps16 intron, phylogeny, southern Africa, Umbelliferae.


Kew Bulletin ◽  
2002 ◽  
Vol 57 (1) ◽  
pp. 183 ◽  
Author(s):  
James J. Clarkson ◽  
Mark W. Chase ◽  
Madeline M. Harley

Author(s):  
G. Stöffler ◽  
R.W. Bald ◽  
J. Dieckhoff ◽  
H. Eckhard ◽  
R. Lührmann ◽  
...  

A central step towards an understanding of the structure and function of the Escherichia coli ribosome, a large multicomponent assembly, is the elucidation of the spatial arrangement of its 54 proteins and its three rRNA molecules. The structural organization of ribosomal components has been investigated by a number of experimental approaches. Specific antibodies directed against each of the 54 ribosomal proteins of Escherichia coli have been performed to examine antibody-subunit complexes by electron microscopy. The position of the bound antibody, specific for a particular protein, can be determined; it indicates the location of the corresponding protein on the ribosomal surface.The three-dimensional distribution of each of the 21 small subunit proteins on the ribosomal surface has been determined by immuno electron microscopy: the 21 proteins have been found exposed with altogether 43 antibody binding sites. Each one of 12 proteins showed antibody binding at remote positions on the subunit surface, indicating highly extended conformations of the proteins concerned within the 30S ribosomal subunit; the remaining proteins are, however, not necessarily globular in shape (Fig. 1).


Author(s):  
Neng-Yu Zhang ◽  
Terence Wagenknecht ◽  
Michael Radermacher ◽  
Tom Obrig ◽  
Joachim Frank

We have reconstructed the 40S ribosomal subunit at a resolution of 4 nm using the single-exposure pseudo-conical reconstruction method of Radermacher et al.Small (40S) ribosomal subunits were Isolated from rabbit reticulocytes, applied to grids and negatively stained (0.5% uranyl acetate) in a manner that “sandwiches” the specimen between two layers of carbon. Regions of the grid exhibiting uniform and thick staining were identified and photographed twice (magnification 49,000X). The first micrograph was always taken with the specimen tilted by 50° and the second was of the Identical area untilted (Fig. 1). For each of the micrographs the specimen was subjected to an electron dose of 2000-3000 el/nm2.Three hundred thirty particles appearing in the L view (defined in [4]) were selected from both tilted- and untilted-specimen micrographs. The untilted particles were aligned and their rotational alignment produced the azimuthal angles of the tilted particles in the conical tilt series.


Author(s):  
M. Boublik ◽  
V. Mandiyan ◽  
J.F. Hainfeld ◽  
J.S. Wall

The aim of this study is to understand the mechanism of 16S rRNA folding into the compact structure of the small 30S subunit of E. coli ribosome. The assembly of the 30S E. coli ribosomal subunit is a sequence of specific interactions of 16S rRNA with 21 ribosomal proteins (S1-S21). Using dedicated high resolution STEM we have monitored structural changes induced in 16S rRNA by the proteins S4, S8, S15 and S20 which are involved in the initial steps of 30S subunit assembly. S4 is the first protein to bind directly and stoichiometrically to 16S rRNA. Direct binding also occurs individually between 16S RNA and S8 and S15. However, binding of S20 requires the presence of S4 and S8. The RNA-protein complexes are prepared by the standard reconstitution procedure, dialyzed against 60 mM KCl, 2 mM Mg(OAc)2, 10 mM-Hepes-KOH pH 7.5 (Buffer A), freeze-dried and observed unstained in dark field at -160°.


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