Faculty Opinions recommendation of tRNAs in Trypanosoma brucei: genomic organization, expression, and mitochondrial import.

Author(s):  
C Graham Clark
2002 ◽  
Vol 22 (11) ◽  
pp. 3707-3717 ◽  
Author(s):  
Timothy H. P. Tan ◽  
Roland Pach ◽  
Anne Crausaz ◽  
Al Ivens ◽  
André Schneider

ABSTRACT The mitochondrial genome of Trypanosoma brucei does not encode tRNAs. Consequently, all mitochondrial tRNAs are imported from the cytosol and originate from nucleus-encoded genes. Analysis of all currently available T. brucei sequences revealed that its genome carries 50 tRNA genes representing 40 different isoacceptors. The identified set is expected to be nearly complete since all but four codons are accounted for. The number of tRNA genes in T. brucei is very low for a eukaryote and lower than those of many prokaryotes. Using quantitative Northern analysis we have determined the absolute abundance in the cell and the mitochondrion of a group of 15 tRNAs specific for 12 amino acids. Except for the initiator type tRNAMet, which is cytosol specific, the cytosolic and the mitochondrial sets of tRNAs were qualitatively identical. However, the extent of mitochondrial localization was variable for the different tRNAs, ranging from 1 to 7.5% per cell. Finally, by using transgenic cell lines in combination with quantitative Northern analysis it was shown that import of tRNALeu(CAA) is independent of its 5′-genomic context, suggesting that the in vivo import substrate corresponds to the mature, fully processed tRNA.


1996 ◽  
Vol 79 (1) ◽  
pp. 119-123 ◽  
Author(s):  
Evelyn L. Ridgley ◽  
Zhao-hui Xiong ◽  
Kiran J. Kaur ◽  
Larry Ruben

1983 ◽  
Vol 9 (3) ◽  
pp. 255-269 ◽  
Author(s):  
Marilyn Parsons ◽  
Richard G. Nelson ◽  
George Newport ◽  
Michael Milhausen ◽  
Kenneth Stuart ◽  
...  

2020 ◽  
Author(s):  
Ujjal K. Singha ◽  
Anuj Tripathi ◽  
Joseph T. Smith ◽  
Linda Quinones ◽  
Aparajita Saha ◽  
...  

1983 ◽  
Vol 23 (1-4) ◽  
pp. 27-33 ◽  
Author(s):  
Marilyn Parsons ◽  
Richard G. Nelson ◽  
Kenneth Stuart ◽  
Nina Agabian

Planta Medica ◽  
2013 ◽  
Vol 79 (13) ◽  
Author(s):  
MS Nogueira ◽  
FB da Costa ◽  
MA Magenta ◽  
M Kaiser ◽  
R Brun ◽  
...  

1994 ◽  
Vol 71 (05) ◽  
pp. 651-654 ◽  
Author(s):  
Rainer Kalb ◽  
Sentot Santoso ◽  
Katja Unkelbach ◽  
Volker Kiefel ◽  
Christian Mueller-Eckhardt

SummaryAlloimmunization against the human platelet alloantigen system Br (HPA-5) is the second most common cause of neonatal alloimmune thrombocytopenia (NAIT) in Caucasian populations. We have recently shown that a single base polymorphism at position 1648 on platelet mRNA coding for GPIa results in an aminoacid substitution at position 505 on the mature GPIa which is associated with the two serological defined Br phenotypes.Since DNA-typing of platelet alloantigens offers possibilities for useful clinical applications, we designed genomic DNA-based restriction fragment length polymorphism (RFLP) typing for Br alloantigens. To establish this technique we analyzed the genomic organization of GPIa adjacent to the polymorphic base. Using the polymerase chain reaction (PCR) of blood cell DNA we have identified two introns (approximately 1.7 and 1.9 kb) flanking a 144 bp coding sequence of the GPIa gene encompassing the polymorphic base 1648. Based on the in- tron sequence, a PCR primer was constructed to amplify a 274 bp fragment which was used for allele-specific RFLP to determine the Br genotypes. The results of RFLP analysis using Mnll endonuclease obtained from 15 donors (2 Br37*, 2 Br^ and 11 Brb/b) correlate perfectly with serological typing by monoclonal antibody-specific immobilization of platelet antigens (MAIPA) assay.


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