Functional characterization and physiological significance of SETD3

Lysine methyltransferase family plays important roles in various cellular processes, for instance transcriptional regulation, embryonic development, cell proliferation, migration and more. My project aims to characterize a novel SET-domain containing lysine methyltransferase SETD3 and understand the...

全面介紹

Saved in:
書目詳細資料
主要作者: Chia, Shyh Jenn
其他作者: Su I-Hsin
格式: Theses and Dissertations
語言:English
出版: 2017
主題:
在線閱讀:http://hdl.handle.net/10356/72760
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!
機構: Nanyang Technological University
語言: English
id sg-ntu-dr.10356-72760
record_format dspace
spelling sg-ntu-dr.10356-727602023-02-28T18:36:20Z Functional characterization and physiological significance of SETD3 Chia, Shyh Jenn Su I-Hsin School of Biological Sciences DRNTU::Science::Biological sciences Lysine methyltransferase family plays important roles in various cellular processes, for instance transcriptional regulation, embryonic development, cell proliferation, migration and more. My project aims to characterize a novel SET-domain containing lysine methyltransferase SETD3 and understand the physiological significance of this protein. SET-domain containing protein SETD3 methylates Lys-4 and Lys-36 of histone 3, which is linked to the transcriptional activation. In addition, SETD3 also comprises of Rubisco LSMT C-terminal substrate binding domain that could potentially facilitate binding to non-histone substrate. In our preliminary studies, we identified that SETD3 was able to methylate a 42kDa protein in the cytosolic fraction. According to the size estimation, we conducted SETD3 methylation assays with monomeric and polymeric form of actin. The result showed that monomeric and polymeric actin were the potent substrates of SETD3. From other studies, actin is shown to be methylated at Lys-84 and Lys-326 but the methyltransferases responsible for these methylations remain unknown. In the assays using actin mutants with Lys-84, Lys-326 or Lys-328 to alanine substitutions as substrate, SETD3 methylation activity was not reduced, suggesting that these lysines are unlikely to be the SETD3 target sites. In addition, SETD3 expression in B cells increased after the stimulation with anti-IgM antibodies, thymus-dependent signal CD40 and lipopolysaccharides (LPS). The preliminary flow cytometry immunophenotyping also revealed perturbed development of T cells, B cells, and neutrophils in the conditional SETD3-deficient mice (Mx-cre). These results suggest that SETD3 may play physiological roles in the development, activation, and effector functions of various immune cells. In future, the physiological function of SETD3 in the development of immune cells and immune responses will be further examined using our conditional knockout mouse model. ​Doctor of Philosophy (SBS) 2017-11-11T01:37:35Z 2017-11-11T01:37:35Z 2017 Thesis Chia, S. J. (2017). Functional characterization and physiological significance of SETD3. Doctoral thesis, Nanyang Technological University, Singapore. http://hdl.handle.net/10356/72760 10.32657/10356/72760 en 64 p. application/pdf
institution Nanyang Technological University
building NTU Library
continent Asia
country Singapore
Singapore
content_provider NTU Library
collection DR-NTU
language English
topic DRNTU::Science::Biological sciences
spellingShingle DRNTU::Science::Biological sciences
Chia, Shyh Jenn
Functional characterization and physiological significance of SETD3
description Lysine methyltransferase family plays important roles in various cellular processes, for instance transcriptional regulation, embryonic development, cell proliferation, migration and more. My project aims to characterize a novel SET-domain containing lysine methyltransferase SETD3 and understand the physiological significance of this protein. SET-domain containing protein SETD3 methylates Lys-4 and Lys-36 of histone 3, which is linked to the transcriptional activation. In addition, SETD3 also comprises of Rubisco LSMT C-terminal substrate binding domain that could potentially facilitate binding to non-histone substrate. In our preliminary studies, we identified that SETD3 was able to methylate a 42kDa protein in the cytosolic fraction. According to the size estimation, we conducted SETD3 methylation assays with monomeric and polymeric form of actin. The result showed that monomeric and polymeric actin were the potent substrates of SETD3. From other studies, actin is shown to be methylated at Lys-84 and Lys-326 but the methyltransferases responsible for these methylations remain unknown. In the assays using actin mutants with Lys-84, Lys-326 or Lys-328 to alanine substitutions as substrate, SETD3 methylation activity was not reduced, suggesting that these lysines are unlikely to be the SETD3 target sites. In addition, SETD3 expression in B cells increased after the stimulation with anti-IgM antibodies, thymus-dependent signal CD40 and lipopolysaccharides (LPS). The preliminary flow cytometry immunophenotyping also revealed perturbed development of T cells, B cells, and neutrophils in the conditional SETD3-deficient mice (Mx-cre). These results suggest that SETD3 may play physiological roles in the development, activation, and effector functions of various immune cells. In future, the physiological function of SETD3 in the development of immune cells and immune responses will be further examined using our conditional knockout mouse model.
author2 Su I-Hsin
author_facet Su I-Hsin
Chia, Shyh Jenn
format Theses and Dissertations
author Chia, Shyh Jenn
author_sort Chia, Shyh Jenn
title Functional characterization and physiological significance of SETD3
title_short Functional characterization and physiological significance of SETD3
title_full Functional characterization and physiological significance of SETD3
title_fullStr Functional characterization and physiological significance of SETD3
title_full_unstemmed Functional characterization and physiological significance of SETD3
title_sort functional characterization and physiological significance of setd3
publishDate 2017
url http://hdl.handle.net/10356/72760
_version_ 1759854412899024896