Ulla B. Godwin
East Carolina University
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Featured researches published by Ulla B. Godwin.
Immunogenetics | 1995
J.J. Hardee; Ulla B. Godwin; R. Benedetto; Thomas J. McConnell
Adaptions of the polymerase chain reaction were used to isolate cDNA sequences encoding the Major histocompatibility complex(Mhc) class II A gene(s) of the striped bass (Morone saxatilis). Four complete Mhc class II A genes were cloned and sequenced from a specimen originating in the Roanoke River, North Carolina, and another three A genes from a specimen originating from the Santee-Cooper Reservoir, South Carolina, identifying a total of seven unique sequences. The sequence suggests the presence of at least two Mhc class II A loci. The extensive sequence variability observed between the seven different Mhc class II clones was concentrated in the α1 encoding domain. The encoded α2, transmembrane, and cytoplasmic regions of all seven striped genes correlated well with those of known vertebrate Mhc class II proteins. Overall, the striped bass sequences showed greatest similarity to the Mhc class II A genes of the zebrafish. Southern blot analysis demonstrated extensive polymorphism in the Mhc class II A genes in members of a Roanoke river-caught population of striped bass versus a lesser degree of polymorphism in an aquacultured Santee-Cooper population of striped bass.
Marine Biotechnology | 1999
Robert J. Hogan; Geoffrey C. Waldbieser; Cheryl A. Goudie; Aurita Antao; Ulla B. Godwin; Melanie Wilson; Norman W. Miller; L. William Clem; Thomas J. McConnell; William R. Wolters; V. Gregory Chinchar
Abstract: Second-generation gynogenetic channel catfish were characterized by molecular and immunologic assays to determine if they were isogenic at major histocompatibility complex loci. Southern blot analyses, using channel catfish MHC class II B and class I A gene probes, revealed identical banding patterns among second-generation gynogenetic fish. In contrast, banding patterns from outbred fish differed not only from gynogenetic animals, but also among themselves. Nucleotide sequence analysis of the MHC class II β1 domain, which encompasses the peptide binding region, from four randomly selected gynogenetic fish showed a single DNA sequence. In contrast, analysis of the same region from three outbred fish showed sequences that differed not only among themselves, but also from those of gynogenetic animals. In cytotoxic assays, peripheral blood leukocytes from outbred fish lysed both gynogenetic and allogeneic targets, whereas those from gynogenetic fish lysed only allogeneic targets. Taken together, these results suggest that this group of second-generation gynogenetic channel catfish is isogenic at MHC loci and may provide an excellent system with which to study cell-mediated immunity in teleosts.
Immunological Reviews | 1998
Thomas J. McConnell; Ulla B. Godwin; Brandon J. Cuthbertson
Summary: Peptides derived from parasites are presented to T helper cells by major histocompatibility complex (MHC) class II αβ heterotrimeric cell‐surface molecules. In mice and humans, the genes encoding these antigen‐presenting molecules are known to be polymorphic and poly‐genic. Multiple loci for MHC class II A and E genes are proposed to allow for an increased peptide‐binding repertoire. The multigenic nature of expressed MHC class II loci and the differences between these loci in fishes are the focus of this review, Particular emphasis is placed on an evolutionary comparison of class II B loci, especially two class 11 B loci that have undergone dramatic changes from one another suggesting an ancestral gene duplication event that took place at an early stage in the evolution of teleosts, The number of functional class II αβ loci heterotrimers may have a profound impact on the organisms ability to battle constantly evolving parasitic infections.
Immunogenetics | 2004
Kelly E. Roney; Brandon J. Cuthbertson; Ulla B. Godwin; Steven Kazianis; Luis Della Coletta; Gil G. Rosenthal; Michael J. Ryan; Margit Schmidt; Thomas J. McConnell
Classical MHC class II glycoproteins present peptides to T cells. In Xiphophorus fishes and in the guppy, Poecilia reticulata, a classical MHC class II B-like transcript has been identified, DAB, as well as a divergent MHC class II B-like transcript, DXB. In the two species of Xiphophorus fishes studied here, X. multilineatus and X. pygmaeus, alternative splicing of the DXB transcript was observed, but not of the classical type DAB transcripts. Two alternative splice patterns were found: a 16-codon deletion and a five-nucleotide deletion that leads to an extension of the transcript. A single DXB transcript that terminates before the transmembrane region was also observed. The alternative splice pattern and the divergence of DXB from DAB suggest that in fish, DXB may have an alternate function. Alternative splicing transcripts of DXB may allow for signaling and localization of DXB within the cell.
Veterinary Immunology and Immunopathology | 2008
Mohadetheh Moulana; Jason P. Evenhuis; Mark Albertino; Ulla B. Godwin; Evgueni Kountikov; Tor B. Stuge; Melanie Wilson; Eva Bengtén; Norman W. Miller; Thomas J. McConnell
This study characterizes four monoclonal antibodies (mAb) developed against the major histocompatibility complex (MHC) class II beta chain of the channel catfish, Ictalurus punctatus. Immunoprecipitations using catfish clonal B cells revealed that each of these mAbs immunoselected proteins of approximately 32 and 36 kD, which are of the appropriate sizes for MHC class II alpha and beta chains, respectively. Cell distribution studies using a fluorescence-activated cell sorter (FACS) combined with RT-PCR analyses demonstrated that MHC class II beta is expressed at a high density on catfish clonal macrophage, B and T cell lines, on alloantigen stimulated leukocytes, and on lipopolysaccharide-induced B-cell blasts. Collectively, these results demonstrate the potential importance of these antibodies as reagents in future studies dealing with the functional role of MHC class II molecules in immune recognition of self from non-self.
Developmental and Comparative Immunology | 1997
Ulla B. Godwin; Mike Flores; Sylvie M. A. Quiniou; Melanie Wilson; Norman W. Miller; L. William Clem; Thomas J. McConnell
Genetics | 1998
Thomas J. McConnell; Ulla B. Godwin; Stephen F. Norton; Rodney S. Nairn; Steven Kazianis; Donald C. Morizot
Developmental and Comparative Immunology | 2004
James R. Fuller; Joshua E. Pitzer; Ulla B. Godwin; Mark Albertino; Benjamin D Machon; Kelly P. Kearse; Thomas J. McConnell
Developmental and Comparative Immunology | 2006
Anil Thankappan; James R. Fuller; Ulla B. Godwin; Kelly P. Kearse; Thomas J. McConnell
Archive | 2000
Ulla B. Godwin; Michael Flores; Thomas J. McConnell; Melanie Wilson; Sylvie M. A. Quiniou; Norman W. Miller; L. William Clem