Please use this identifier to cite or link to this item: http://hdl.handle.net/10603/426115
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dc.date.accessioned2022-12-17T07:14:35Z-
dc.date.available2022-12-17T07:14:35Z-
dc.identifier.urihttp://hdl.handle.net/10603/426115-
dc.description.abstractCellular events that rely on translation regulation has been well established, however the molecular details of factors involved in bringing translation control remains inadequately explored. RNA binding proteins form an integral part of transcriptional and post-transcriptional gene regulation pathway. However, the principles that govern the activity of an RNA binding protein is poorly explored. In this thesis, a systematic investigation has been done to delineate the contribution of individual RRM domains and arginine methylation in the RGG motif of an RNA binding protein, Sbp1 towards its function. Chapter 3 demonstrated that role of arginine methylation of Sbp1 RGG motif towards its translation repression and decapping enhancing activity. Pull-down assays indicated that Sbp1 interaction with eIF4G1 decreases when the methylating enzyme, Hmt1 is absent or the Sbp1 RGG motif is deleted. We also learned that Sbp1 mono-methylation increases upon glucose starvation stress, which is known to cause global translation repression in yeast. Moreover, arginine methylation of Sbp1 was found to be crucial for driving decapping activators such as Dhh1 and Scd6 to RNA granules. Together, our results have established functional relevance of arginine methylation towards translation repression and decapping enhancing ability of RNA binding protein, Sbp1. Chapter 4 investigated the role of RRM domains of Sbp1 towards causing over-expression mediated growth defect and localizing to RNA granules. RRM domains are the most abundant RNA binding domain that harbor 6-8 amino acid consensus sequence involved in RNA binding. Our results have demonstrated that upon deleting both the RRM domains and not the RNP sequence, SBP1 over-expression mediated growth defect can be rescued. Moreover, and#8710;RRM 1+2 mutant of Sbp1 could not localize to RNA granules upon glucose starvation than wild-type. These observations suggest that Sbp1 RRM domains function via sequences outside the RNP motif, which is yet to be discovered...-
dc.format.extent185-
dc.languageEnglish-
dc.rightsuniversity-
dc.titleUnderstanding mRNA fate regulation by RGG motif protein Sbp1-
dc.title.alternativeUnderstanding mRNA fate regulation by RGG motif protein, Sbp1-
dc.creator.researcherBhatter, Nupur-
dc.subject.keywordChemistry-
dc.subject.keywordChemistry Multidisciplinary-
dc.subject.keywordmRNA fate-
dc.subject.keywordPhysical Sciences-
dc.subject.keywordRGG motif protein-
dc.contributor.guideRajyaguru, Purusharth I-
dc.publisher.placeBangalore-
dc.publisher.universityIndian Institute of Science Bangalore-
dc.publisher.institutionBiochemistry-
dc.date.completed2021-
dc.date.awarded2022-
dc.format.dimensions30cm-
dc.format.accompanyingmaterialNone-
dc.source.universityUniversity-
dc.type.degreePh.D.-
Appears in Departments:Biochemistry

Files in This Item:
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01_title.pdfAttached File38.55 kBAdobe PDFView/Open
02_prelim pages.pdf305.1 kBAdobe PDFView/Open
03_contents.pdf195.7 kBAdobe PDFView/Open
04_abstract.pdf164.98 kBAdobe PDFView/Open
05_chapter 1.pdf1.25 MBAdobe PDFView/Open
06_chapter 2.pdf368.7 kBAdobe PDFView/Open
07_chapter 3.pdf940.73 kBAdobe PDFView/Open
08_chapter 4.pdf933.11 kBAdobe PDFView/Open
09_chapter 5.pdf1.78 MBAdobe PDFView/Open
10_annexure.pdf256.15 kBAdobe PDFView/Open
80_recommendation.pdf153.38 kBAdobe PDFView/Open


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