東華大學圖書館 |

語系: 繁體中文

說明(常見問題)

回圖書館首頁

手機版館藏查詢

登入

回首頁

切換: 標籤 | MARC模式 | ISBD

Multiple layers of gene expression r...

Lu, Rong.

FindBook

Google Book

Amazon

博客來

Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation.

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
正題名/作者:	Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation./
作者:	Lu, Rong.
面頁冊數:	153 p.
附註:	Source: Dissertation Abstracts International, Volume: 68-03, Section: B, page: 1440.
Contained By:	Dissertation Abstracts International68-03B.
標題:	Biology, Bioinformatics. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3256579

Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation.
Lu, Rong.

Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation. - 153 p.

Source: Dissertation Abstracts International, Volume: 68-03, Section: B, page: 1440.

Thesis (Ph.D.)--Princeton University, 2007.

Gene expression is regulated at several distinct steps: modulation of chromatin structure, transcription, RNA processing, and translation. We have explored the contribution of all four layers of gene expression regulations to the development of murine embryonic stem (ES) cells. ES cells were induced to differentiate by down regulating a single gene, Nanog. Dynamic changes in chromatin structure, RNA transcription, RNA level, and final protein product were recorded using global measurement techniques, including RNA microarray, ChIP-on-chip and iTRAQ based mass spectrometry. Different patterns of gene expression regulatory events were analyzed using bioinformatic and statistic tools. Positive correlations between different gene expression steps were observed. We have also observed a time delay for chromatin structure change to affect gene expression change. Comparison between RNA polymerase attachment and RNA level suggests a possible role of post transcription regulation. There is evidence for a multifaceted regulation of protein production. About 40% of the protein changes are not correlated with RNA changes during this ES cell differentiation process, suggesting regulation at the translational or post translational levels. Post transcription control may determine the change of about 22% of the proteins. Modulation of chromatin structure and transcription may each determine the change of about 16% of the proteins. We have also found that genes with the same function are co-regulated at the same gene expression control step. We have reported the epigenetic change during ES cell differentiation in terms of histone isoforms change at the protein level and genomic histone acetylation dynamics at individual gene promoters. Our data on the multiple layers of gene expression after Nanog down regulation also allows for a deeper understanding of the Nanog downstream genes and Nanog binding genes. It helps to decipher the gene expression events during early ES cell differentiation. This is the first concerted epigenome, transcriptome, and proteome dynamic analysis.Subjects--Topical Terms:

1018415
Biology, Bioinformatics.

Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation.
LDR:02928nam 2200253 a 45 001 948222
005 20110524
008 110524s2007 ||||||||||||||||| ||eng d
035 $a (UMI)AAI3256579
035 $a AAI3256579
040 $a UMI $c UMI
100 1 $a Lu, Rong. $3 1271682
245 1 0 $a Multiple layers of gene expression regulation during murine embryonic stem cell differentiation induced by Nanog down regulation.
300 $a 153 p.
500 $a Source: Dissertation Abstracts International, Volume: 68-03, Section: B, page: 1440.
502 $a Thesis (Ph.D.)--Princeton University, 2007.
520 $a Gene expression is regulated at several distinct steps: modulation of chromatin structure, transcription, RNA processing, and translation. We have explored the contribution of all four layers of gene expression regulations to the development of murine embryonic stem (ES) cells. ES cells were induced to differentiate by down regulating a single gene, Nanog. Dynamic changes in chromatin structure, RNA transcription, RNA level, and final protein product were recorded using global measurement techniques, including RNA microarray, ChIP-on-chip and iTRAQ based mass spectrometry. Different patterns of gene expression regulatory events were analyzed using bioinformatic and statistic tools. Positive correlations between different gene expression steps were observed. We have also observed a time delay for chromatin structure change to affect gene expression change. Comparison between RNA polymerase attachment and RNA level suggests a possible role of post transcription regulation. There is evidence for a multifaceted regulation of protein production. About 40% of the protein changes are not correlated with RNA changes during this ES cell differentiation process, suggesting regulation at the translational or post translational levels. Post transcription control may determine the change of about 22% of the proteins. Modulation of chromatin structure and transcription may each determine the change of about 16% of the proteins. We have also found that genes with the same function are co-regulated at the same gene expression control step. We have reported the epigenetic change during ES cell differentiation in terms of histone isoforms change at the protein level and genomic histone acetylation dynamics at individual gene promoters. Our data on the multiple layers of gene expression after Nanog down regulation also allows for a deeper understanding of the Nanog downstream genes and Nanog binding genes. It helps to decipher the gene expression events during early ES cell differentiation. This is the first concerted epigenome, transcriptome, and proteome dynamic analysis.
590 $a School code: 0181.
650 4 $a Biology, Bioinformatics. $3 1018415
650 4 $a Biology, Cell. $3 1017686
650 4 $a Biology, Molecular. $3 1017719
690 $a 0307
690 $a 0379
690 $a 0715
710 2 0 $a Princeton University. $3 645579
773 0 $t Dissertation Abstracts International $g 68-03B.
790 $a 0181
791 $a Ph.D.
792 $a 2007
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3256579