SprD

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__NOTOC__ In molecular biology SprD (Small pathogenicity island RNA D) is a non-coding RNA expressed on pathogenicity islands in Staphylococcus aureus. It was identified in silico along with a number of other sRNAs (SprA-G) through microarray analysis which were confirmed using a Northern blot. SprD has been found to significantly contribute to causing disease in an animal model.

__NOTOC__ In molecular biology SprD (Small pathogenicity island RNA D) is a non-coding RNA expressed on pathogenicity islands in Staphylococcus aureus. It was identified in silico along with a number of other sRNAs (SprA-G) through microarray analysis which were confirmed using a Northern blot. SprD has been found to significantly contribute to causing disease in an animal model. ==Function== SprD is located between genes scn and chp in the innate immune evasion cluster (IEC) of the S. aureus genome. Its placement within this region was the first indication of a virulence-factor regulatory function. SprD binds with sbi (Staphylococcus aureus binder of IgG) mRNA which encodes an immune evasion protein. It occludes the Shine-Dalgarno sequence and the initiation codon of sbi, forming a sbi mRNA-SprD duplex repressing the translation of the mRNA. sbi protein interferes with the host's innate immune response by binding Factor H, Complement component 3 and IgG. ==See also== Protein A SprX ==References== ==Further reading== ==External links==

Text derived from https://en.wikipedia.org/w/index.php?oldid=1314988301 under CC BY-SA 4.0; modifications have been made.

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