國立虎尾科技大學 |

Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma.

紀錄類型:	書目-語言資料,手稿 : Monograph/item
正題名/作者:	Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma./
作者:	Zhang, Sharon X.
面頁冊數:	1 online resource (85 pages)
附註:	Source: Masters Abstracts International, Volume: 57-05.
Contained By:	Masters Abstracts International57-05(E).
標題:	Information science. -
電子資源:	click for full text (PQDT)
ISBN:	9780355708578

Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma.
Zhang, Sharon X.

Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma. - 1 online resource (85 pages)

Source: Masters Abstracts International, Volume: 57-05.

Thesis (M.S.)--San Diego State University, 2018.

Includes bibliographical references

Intermittent fasting (IF) has been shown to have a positive impact on aging Drosophila, which included promoting longevity, lowering neural aggregates and improving behavior and autophagy responses in middle-aged flies. In a separate traumatic brain injury (TBI) model, we determined that repetitive bouts of injury had long-term negative consequences to longevity and neural function. Understanding the impact that aging, diet and TBI exposure has on the cellular and molecular response of the CNS could identify the conserved mechanisms that influence aging and trauma responses in human and mammalian systems and the development of potential treatments or therapies. Using the recent advances in RNA sequencing, tissues from IF and TBI Drosophila models were used for the transcriptional analysis of genes and functional pathways influenced by aging, diet and injury. The work outlined in this proposal used bioinformatics techniques to analyze RNAsequencing data generated from adult tissues taken at different ages or exposed to IF and TBI treatment conditions. For aged and IF-treated mRNA profiles, we developed an analytical pipeline that examined fold and variance changes from replicates within individual tissue datasets. Tissue-specific expression changes to metabolic, behavioral and proteolytic pathways were identified and correlated with the progressive dysregulation of key phenotypes. Much of this work centered on the novel concept that age-dependent increase "transcriptional drift" variance was suppressed following IF-treatment, thus partly restoring more youthful expression and phenotypic profiles. Preliminary analysis of TBI RNA-seq datasets has identified both acute and delayed changes (fold) to molecular pathways involved with inflammatory responses, wound healing, DNA repair, histone modification, and chromatin remodeling responses following TBI exposure. Through this analysis, both studies have useful insights into some of the complex molecular mechanism that are impacted with age and following IF-treatment and TBI exposure. A consistent finding from both RNA-seq studies was the fold change in epigenetic pathway components. The implications are that data mining of multiple RNA-seq datasets can identify profound in vivo changes to key molecular mechanisms that are impacted by aging, diet and trauma.

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

Mode of access: World Wide Web

ISBN: 9780355708578Subjects--Topical Terms:

561178
Information science.
Index Terms--Genre/Form:

554714
Electronic books.

Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma.
LDR:03641ntm a2200349Ki 4500 001 920707
005 20181203094032.5
006 m o u
007 cr mn||||a|a||
008 190606s2018 xx obm 000 0 eng d
020 $a 9780355708578
035 $a (MiAaPQ)AAI10747357
035 $a (MiAaPQ)sdsu:12214
035 $a AAI10747357
040 $a MiAaPQ $b eng $c MiAaPQ $d NTU
100 1 $a Zhang, Sharon X. $3 1195578
245 1 0 $a Data Mining of Two Large Transcriptomic Data Sets that Utilize Drosophila as a Model System for the Study of Neurodegeneration due to Aging and Trauma.
264 0 $c 2018
300 $a 1 online resource (85 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: Masters Abstracts International, Volume: 57-05.
500 $a Adviser: ROBERT EDWARDS.
502 $a Thesis (M.S.)--San Diego State University, 2018.
504 $a Includes bibliographical references
520 $a Intermittent fasting (IF) has been shown to have a positive impact on aging Drosophila, which included promoting longevity, lowering neural aggregates and improving behavior and autophagy responses in middle-aged flies. In a separate traumatic brain injury (TBI) model, we determined that repetitive bouts of injury had long-term negative consequences to longevity and neural function. Understanding the impact that aging, diet and TBI exposure has on the cellular and molecular response of the CNS could identify the conserved mechanisms that influence aging and trauma responses in human and mammalian systems and the development of potential treatments or therapies. Using the recent advances in RNA sequencing, tissues from IF and TBI Drosophila models were used for the transcriptional analysis of genes and functional pathways influenced by aging, diet and injury. The work outlined in this proposal used bioinformatics techniques to analyze RNAsequencing data generated from adult tissues taken at different ages or exposed to IF and TBI treatment conditions. For aged and IF-treated mRNA profiles, we developed an analytical pipeline that examined fold and variance changes from replicates within individual tissue datasets. Tissue-specific expression changes to metabolic, behavioral and proteolytic pathways were identified and correlated with the progressive dysregulation of key phenotypes. Much of this work centered on the novel concept that age-dependent increase "transcriptional drift" variance was suppressed following IF-treatment, thus partly restoring more youthful expression and phenotypic profiles. Preliminary analysis of TBI RNA-seq datasets has identified both acute and delayed changes (fold) to molecular pathways involved with inflammatory responses, wound healing, DNA repair, histone modification, and chromatin remodeling responses following TBI exposure. Through this analysis, both studies have useful insights into some of the complex molecular mechanism that are impacted with age and following IF-treatment and TBI exposure. A consistent finding from both RNA-seq studies was the fold change in epigenetic pathway components. The implications are that data mining of multiple RNA-seq datasets can identify profound in vivo changes to key molecular mechanisms that are impacted by aging, diet and trauma.
533 $a Electronic reproduction. $b Ann Arbor, Mich. : $c ProQuest, $d 2018
538 $a Mode of access: World Wide Web
650 4 $a Information science. $3 561178
650 4 $a Biology. $3 599573
650 4 $a Medicine. $3 644133
655 7 $a Electronic books. $2 local $3 554714
690 $a 0723
690 $a 0306
690 $a 0564
710 2 $a ProQuest Information and Learning Co. $3 1178819
710 2 $a San Diego State University. $b Bioinformatics and Medical Informatics. $3 1195568
773 0 $t Masters Abstracts International $g 57-05(E).
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=10747357 $z click for full text (PQDT)