國立虎尾科技大學 |

Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence.

Record Type:	Language materials, manuscript : Monograph/item
Title/Author:	Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence./
Author:	Rutledge, Mark Taylor, II.
Description:	1 online resource (145 pages)
Notes:	Source: Dissertation Abstracts International, Volume: 78-11(E), Section: B.
Contained By:	Dissertation Abstracts International78-11B(E).
Subject:	Molecular biology. -
Online resource:	click for full text (PQDT)
ISBN:	9780355039474

Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence.
Rutledge, Mark Taylor, II.

Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence. - 1 online resource (145 pages)

Source: Dissertation Abstracts International, Volume: 78-11(E), Section: B.

Thesis (Ph.D.)--Princeton University, 2017.

Includes bibliographical references

Eukaryotic DNA is packaged into chromatin, a nucleo-protein structure influencing various cellular functions. I was interested in understanding the connections between chromatin structure, gene expression, and cellular physiology in Saccharomyces cerevisiae during the extreme growth transition from exponential growth to quiescence. I thus measured genome-wide chromatin and proteomic changes during this transition.

Electronic reproduction.
Ann Arbor, Mich. :
ProQuest,
2018

Mode of access: World Wide Web

ISBN: 9780355039474Subjects--Topical Terms:

583443
Molecular biology.
Index Terms--Genre/Form:

554714
Electronic books.

Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence.
LDR:04048ntm a2200385Ki 4500 001 918782
005 20181106104110.5
006 m o u
007 cr mn||||a|a||
008 190606s2017 xx obm 000 0 eng d
020 $a 9780355039474
035 $a (MiAaPQ)AAI10266010
035 $a (MiAaPQ)princeton:12067
035 $a AAI10266010
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Rutledge, Mark Taylor, II. $3 1193199
245 1 0 $a Chromatin Structure and Gene Expression in Saccharomyces cerevisiae Quiescence.
264 0 $c 2017
300 $a 1 online resource (145 pages)
336 $a text $b txt $2 rdacontent
337 $a computer $b c $2 rdamedia
338 $a online resource $b cr $2 rdacarrier
500 $a Source: Dissertation Abstracts International, Volume: 78-11(E), Section: B.
500 $a Adviser: James R. Broach.
502 $a Thesis (Ph.D.)--Princeton University, 2017.
504 $a Includes bibliographical references
520 $a Eukaryotic DNA is packaged into chromatin, a nucleo-protein structure influencing various cellular functions. I was interested in understanding the connections between chromatin structure, gene expression, and cellular physiology in Saccharomyces cerevisiae during the extreme growth transition from exponential growth to quiescence. I thus measured genome-wide chromatin and proteomic changes during this transition.
520 $a At the nucleosome level protein-coding genes initially gained nucleosome occupancy on average with later gains occurring over promoter nucleosome depleted regions (NDRs). Individually, NDR occupancy and transcript level changes correlated negatively, especially for genes with large increases in NDR occupancy. Genes in the same functional class displayed similar changes potentially impacting expression via transcription factor binding site (TFBS) occlusion. Rpd3L-, ISWI-, and RSC-related TFBSs had decreased nucleosome occupancy with promoters containing RSC binding sites also having more TFBSs with lower nucleosome occupancy and increased transcript levels.
520 $a At the chromosome level interaction frequency between any two points within a chromosome arm decreased exponentially with increasing linear chromosomal distance for both growth states. Also, intra-arm interactions were more frequent than inter-arm or -chromosomal interactions, and intra-arm interactions formed domains of self-association with variable boundaries between states. These data accompanied by fluorescence microscopy revealed three changes to the spatial organization of chromosomes during quiescence. First, subtelomeric interactions and the number of telomeric foci increased reflecting increases in subtelomeric foci participation. Second, inter-centromeric interactions decreased suggesting spindle pole body reorganization. Third, chromosomes condensed as seen by global decreases in intra-chromosomal interactions and decreased average distance between two intra-chromosomal loci. Furthermore, conditional inactivation of condensin abolished this condensation in a large subpopulation of cells.
520 $a Finally, I measured proteomic changes upon the transition to quiescence induced by different nutrient starvations. Protein and transcript levels tended to concertedly change for nitrogen and phosphate but not glucose starvation. The number of post-starvation cell divisions appeared to govern this correlation. I identified nutrient-specific and -independent proteomic changes, each group enriched for different cellular functions. While many proteins changed in abundance these changes alone were not observed to significantly impact the functions of metabolic enzymes or genes required to survive quiescence when compared to the global proteome.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2018
538 $a Mode of access: World Wide Web
650 4 $a Molecular biology. $3 583443
650 4 $a Cellular biology. $3 1148666
650 4 $a Genetics. $3 578972
655 7 $a Electronic books. $2 local $3 554714
690 $a 0307
690 $a 0379
690 $a 0369
710 2 $a ProQuest Information and Learning Co. $3 1178819
710 2 $a Princeton University. $b Molecular Biology. $3 1193148
773 0 $t Dissertation Abstracts International $g 78-11B(E).
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10266010 $z click for full text (PQDT)