Sandbox Reserved 1328
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== Ribonuclease Inhibitor-Angiogenin Complex== | == Ribonuclease Inhibitor-Angiogenin Complex== | ||
<StructureSection load='1a4y' size='350' side='right' caption='DNA Structure' scene=''> | <StructureSection load='1a4y' size='350' side='right' caption='DNA Structure' scene=''> | ||
- | The ribonuclease inhibitor-angiogenin complex is a protein | + | The ribonuclease inhibitor-angiogenin complex is a protein most concentrated in human placental cells. The ribonuclease inhibitor protein and angiogenin protein have a strong affinity for each other. The main gene that codes for the ribonuclease inhibitor is RNH1. Ribonuclease also inhibits other proteins such as RNASE1 and RNASE2, so it is also important in processing RNA. Angiogenin has a sequence length of 123 and its gene name is ANG or RNASE5. |
== Function == | == Function == | ||
- | The complex is responsible for protein binding and positive regulation of phosphorylation. The ribonuclease inhibitor protein binds to the angiogenin complex, a blood-vessel inducing protein, to inhibit it. Angiogenin is able to promote growth of blood vessels by promoting rRNA transcription. Under normal growth conditions, ANG is located in the nucleus away from the ribonuclease inhibitor to allow for prolific rRNA transcription. However, during periods of stress nuclear ANG is associated with ribonuclease inhibitor in the cytoplasm. This allows ribonuclease inhibitor to inhibit ANG, and prevent excess rRNA transcription allowing for energy to be conserved. | + | The complex is responsible for protein binding and positive regulation of phosphorylation. The ribonuclease inhibitor protein binds to the angiogenin complex, a blood-vessel inducing protein, to inhibit it. Angiogenin is able to promote growth of blood vessels by promoting rRNA transcription. Under normal growth conditions, ANG is located in the nucleus away from the ribonuclease inhibitor to allow for prolific rRNA transcription. However, during periods of stress nuclear ANG is associated with ribonuclease inhibitor in the cytoplasm. This allows ribonuclease inhibitor to inhibit ANG, and prevent excess rRNA transcription allowing for energy to be conserved. Angiogenin also mediates the production of tiRNA, which have been shown to suppress global protein translation of both capped and uncapped mRNA. In response to stress, tiRNAs reprogram protein translation, thereby promoting cell survival. Therefore, ANG is conserved in granules in the cytoplasm to allow it to mediate tiRNA production and help the cell survive. The ribonuclease inhibitor is key in preventing overproduction of the ANG during stress conditions. |
== Relevance == | == Relevance == | ||
- | Angiogenin has been known to be involved in normal and tumor growth during angiogenesis. The presence of inhibitors, such as ribonuclease inhibitor, blocks angiogenin and limits blood vessel growth. This can therefore curb proliferation of cancer cells. Malfunctions in angiogenin are also a main cause of | + | Angiogenin has been known to be involved in normal and tumor growth during angiogenesis. The presence of inhibitors, such as ribonuclease inhibitor, blocks angiogenin and limits blood vessel growth. This can therefore curb proliferation of cancer cells. Malfunctions in angiogenin are also a main cause of amyotrophic lateral sclerosis (ALS), and is the main 'loss-of-function' mutation associated with the disorder. ANG also is a contributor to other neurodegenerative diseases. |
== Structural highlights == | == Structural highlights == |
Revision as of 02:18, 27 February 2018
This Sandbox is Reserved from January through July 31, 2018 for use in the course HLSC322: Principles of Genetics and Genomics taught by Genevieve Houston-Ludlam at the University of Maryland, College Park, USA. This reservation includes Sandbox Reserved 1311 through Sandbox Reserved 1430. |
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Ribonuclease Inhibitor-Angiogenin Complex
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References
https://www.rcsb.org/structure/1a4y https://www.ncbi.nlm.nih.gov/Structure/mmdb/mmdbsrv.cgi?dps=0&uid=1A4Y https://academic.oup.com/abbs/article/40/7/619/622 http://www.ebi.ac.uk/pdbe/entry/pdb/1a4y http://www.uniprot.org/uniprot/P13489 http://jcs.biologists.org/content/126/18/4308 https://pdbj.org/emnavi/quick.php?id=pdb-1a4y