Expression of antibodies using single-open reading frame vector design and polyprotein processing from mammalian cells

2009 ◽  
Vol 25 (3) ◽  
pp. 735-744 ◽  
Author(s):  
Yune Z. Kunes ◽  
Wendy R. Gion ◽  
Emma Fung ◽  
Jochen G. Salfeld ◽  
Rong-Rong Zhu ◽  
...  
mAbs ◽  
2013 ◽  
Vol 5 (4) ◽  
pp. 595-607 ◽  
Author(s):  
Wendy R. Gion ◽  
Rachel A. Davis-Taber ◽  
Dean A. Regier ◽  
Emma Fung ◽  
Limary Medina ◽  
...  

Genome ◽  
1991 ◽  
Vol 34 (1) ◽  
pp. 6-12 ◽  
Author(s):  
Shiv S. Prasad ◽  
Linda J. Harris ◽  
David L. Baillie ◽  
Ann M. Rose

In this paper we present the sequence of an intact Caenorhabditis briggsae transposable element, Tcb2. Tcb2 is 1606 base pairs in length and contains 80 base pair imperfect terminal repeats and a single open reading frame. We have identified blocks of T-rich repeats in the regions 150–200 and 1421–1476 of this element which are conserved in the Caenorhabditis elegans element Tc1. The sequence conservation of these regions in elements from different Caenorhabditis species suggests that they are of functional importance. A single open reading frame corresponding to the major open reading frame of Tc1 is conserved among Tc1, Tcb1, and Tcb2. Comparison of the first 550 nucleotides of the sequence among the three elements has allowed the evaluation of a model proposing an extension of the major open reading frame. Our data support the suggestion that Tc1 is capable of producing a 335 amino acid protein. A comparison of the sequence coding for the amino and carboxy termini of the 273 amino acid transposase from Caenorhabditis Tc1-like elements and Drosophila HB1 showed different amounts of divergence for each of these regions, indicating that the two functional domains have undergone different amounts of selection. Our data are not compatible with the proposal that Tc1-related sequences have been acquired via horizontal transmission. The divergence of Tc1 from the two C. briggsae elements, Tcb1 and Tcb2, indicated that all three elements have been diverging from each other for approximately the same amount of time as the genomes of the two species.Key words: Caenorhabditis, transposable element, sequence comparison.


Cell Research ◽  
2009 ◽  
Vol 19 (3) ◽  
pp. 296-306 ◽  
Author(s):  
Lijian Shao ◽  
Wei Feng ◽  
Yan Sun ◽  
Hao Bai ◽  
Jun Liu ◽  
...  

2008 ◽  
Vol 133 (2) ◽  
pp. 123-135 ◽  
Author(s):  
Niki Vassilaki ◽  
Haralabia Boleti ◽  
Penelope Mavromara

Virology ◽  
1999 ◽  
Vol 265 (1) ◽  
pp. 66-73 ◽  
Author(s):  
C.D. Smart ◽  
W. Yuan ◽  
R. Foglia ◽  
D.L. Nuss ◽  
D.W. Fulbright ◽  
...  

2002 ◽  
Vol 83 (7) ◽  
pp. 1777-1781 ◽  
Author(s):  
María Eugenia Sánchez de la Torre ◽  
Carmelo López ◽  
Oscar Grau ◽  
María Laura García

Citrus psorosis virus (CPsV) causes a citrus disease occurring worldwide. Isolate CPV 4 has a genome with three single-stranded RNAs. The complete sequence of RNA 2 (1643 nucleotides) is reported here. Northern blot hybridization with strand-specific probes showed that most of the encapsidated RNA 2 is of negative polarity, although a small amount of the complementary strand may also be present in particles. The RNA 2 complementary strand contained a single open reading frame encoding a protein of 476 amino acids, which includes a motif resembling a nuclear localization signal. The sequence of this putative protein shows no significant similarity to any other in the databases. In the 3′-terminal untranslated region there is a putative polyadenylation signal. No subgenomic RNAs derived from RNA 2 were detected.


2010 ◽  
Vol 30 (21) ◽  
pp. 5123-5134 ◽  
Author(s):  
Yutaka Suzuki ◽  
J. Bradley Holmes ◽  
Susana M. Cerritelli ◽  
Kiran Sakhuja ◽  
Michal Minczuk ◽  
...  

ABSTRACT RNase H1 in mammalian cells is present in nuclei and mitochondria. Its absence in mitochondria results in embryonic lethality due to the failure to amplify mitochondrial DNA (mtDNA). Dual localization to mitochondria and nuclei results from differential translation initiation at two in-frame AUGs (M1 and M27) of a single mRNA. Here we show that expression levels of the two isoforms depend on the efficiency of translation initiation at each AUG codon and on the presence of a short upstream open reading frame (uORF) resulting in the mitochondrial isoform being about 10% as abundant as the nuclear form. Translation initiation at the M1 AUG is restricted by the uORF, while expression of the nuclear isoform requires reinitiation of ribosomes at the M27 AUG after termination of uORF translation or new initiation by ribosomes skipping the uORF and the M1 AUG. Such translational organization of RNase H1 allows tight control of expression of RNase H1 in mitochondria, where its excess or absence can lead to cell death, without affecting the expression of the nuclear RNase H1.


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