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Eugenia Spanopoulou

Researcher at Icahn School of Medicine at Mount Sinai

Publications -  22
Citations -  2348

Eugenia Spanopoulou is an academic researcher from Icahn School of Medicine at Mount Sinai. The author has contributed to research in topics: V(D)J recombination & RAG2. The author has an hindex of 19, co-authored 22 publications receiving 2313 citations. Previous affiliations of Eugenia Spanopoulou include Howard Hughes Medical Institute & Rockefeller University.

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Functional immunoglobulin transgenes guide ordered B-cell differentiation in Rag-1-deficient mice.

TL;DR: This experimental system demonstrates the competence of the mu HC and kappa LC to direct and regulate the sequential stages of B-cell differentiation, defines the time at which negative selection of self-reactive B cells occurs, and shows that elimination of these cells occurs equally well in the absence of Rag-1 as in its presence.
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Partial V(D)J Recombination Activity Leads to Omenn Syndrome

TL;DR: It is reported here that patients with Omenn syndrome, a severe immunodeficiency characterized by the presence of activated, anergic, oligoclonal T cells, hypereosinophilia, and high IgE levels, bear missense mutations in either the Rag-1 or Rag-2 genes that result in partial activity of the two proteins.
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The Homeodomain Region of Rag-1 Reveals the Parallel Mechanisms of Bacterial and V(D)J Recombination

TL;DR: Once the Rag-1/Rag-2 complex is engaged on the DNA, subsequent cleavage is directed by the heptamer sequence, which remarkably parallels mechanisms that mediate transposition in bacteria and nematodes.
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RAG1 mediates signal sequence recognition and recruitment of RAG2 in V(D)J recombination.

TL;DR: An in vivo one-hybrid DNA binding assay is used to demonstrate that RAG1, in the absence of RAG2, can mediate signal recognition via the nonamer, with the heptamer acting to enhance its binding.
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Dispensable sequence motifs in the RAG-1 and RAG-2 genes for plasmid V(D)J recombination

TL;DR: The results indicate that the N-terminal one-third of RAG-1, including a zinc-finger-like domain, and an acidic domain of R AG-2 are dispensable for activating V(D)J recombination in a fibroblast, although they contribute quantitatively.