The interaction of nucleolin with a short stem-loop structure (NRE) requires two contiguous RNA-binding domains (RED 1+2). The structural basis for RNA recognition by these RBDs was studied using a genetic system in Escherichia coli. Within each of the two domains, we identified several mutations that severely impair interaction with the RNA target. Mutations that alter RNA-binding specificity were also isolated, suggesting the identity of specific contacts between RED 1+2 amino acids and nucleotides within the NRE stem-loop. Our data indicate that both RBDs participate in a joint interaction with the NRE and that each domain uses a different surface to contact the RNA. The constraints provided by these genetic data and previous mutational studies have enabled us to propose a three-dimensional model of nucleolin RED 1+2 bound to the NRE stem-loop.
机构:
COLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USACOLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USA
CACERES, JF
;
KRAINER, AR
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机构:
COLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USACOLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USA
机构:
COLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USACOLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USA
CACERES, JF
;
KRAINER, AR
论文数: 0引用数: 0
h-index: 0
机构:
COLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USACOLD SPRING HARBOR LAB, POB 100, 1 BUNGTOWN RD, COLD SPRING HARBOR, NY 11724 USA