scholarly journals Complete genomic organization of futb encoding a bovine alpha 3- fucosyltransferase: exons in human orthologous genes emerged from ancestral intronic sequences

1999 ◽  
Vol 16 (11) ◽  
pp. 1535-1547 ◽  
Author(s):  
A. Wierinckx ◽  
D. Mercier ◽  
A. Oulmouden ◽  
J. M. Petit ◽  
R. Julien
Genomics ◽  
2004 ◽  
Vol 83 (5) ◽  
pp. 936-939 ◽  
Author(s):  
Karine Rousseau ◽  
Clare Byrne ◽  
Young S. Kim ◽  
James R. Gum ◽  
Dallas M. Swallow ◽  
...  

2000 ◽  
Vol 19 (7) ◽  
pp. 431-446 ◽  
Author(s):  
Jiann-Horng Leu ◽  
Shian-Jang Yan ◽  
Tzuu-Fen Lee ◽  
Chih-Ming Chou ◽  
Shui-Tsung Chen ◽  
...  

2020 ◽  
Vol 501 ◽  
pp. 110657 ◽  
Author(s):  
Ayaka Nishikido ◽  
Takashi Okamura ◽  
Yasuyo Nakajima ◽  
Emi Ishida ◽  
Tomoko Miyamoto ◽  
...  

2003 ◽  
Vol 77 (19) ◽  
pp. 10339-10347 ◽  
Author(s):  
G. Delhon ◽  
M. P. Moraes ◽  
Z. Lu ◽  
C. L. Afonso ◽  
E. F. Flores ◽  
...  

ABSTRACT Here we present the complete genomic sequence of bovine herpesvirus 5 (BHV-5), an alphaherpesvirus responsible for fatal meningoencephalitis in cattle. The 138,390-bp genome encodes 70 putative proteins and resembles the α2 subgroup of herpesviruses in genomic organization and gene content. BHV-5 is very similar to BHV-1, the etiological agent of infectious bovine rhinotracheitis, as reflected by the high level of amino acid identity in their protein repertoires (average, 82%). The highest similarity to BHV-1 products (≥95% amino acid identity) is found in proteins involved in viral DNA replication and processing (UL5, UL15, UL29, and UL39) and in virion proteins (UL14, UL19, UL48, and US6). Among the least conserved (≤75%) are the homologues of immediate-early (IE) proteins BICP0, BICP4, and BICP22, the three proteins being longer in BHV-5 than in BHV-1. The structure of the BHV-5 latency-related (LR) region departs markedly from that of BHV-1 in both coding and transcriptional regulatory regions. Given the potential significance of IE genes and the LR region in virus-neuron interactions, it is likely these differences contribute to BHV-5 neuropathogenicity.


Genomics ◽  
1996 ◽  
Vol 31 (2) ◽  
pp. 223-229 ◽  
Author(s):  
Anthony C. Kim ◽  
Aida B. Metzenberg ◽  
Kenneth E. Sahr ◽  
Shirin M. Marfatia ◽  
Athar H. Chishti

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.


Author(s):  
D. AISINA ◽  
◽  
R. NIYAZOVA ◽  
S. ATAMBAYEVA ◽  
A. IVASHCHENKO ◽  
...  

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