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Investigating the functional implications of the Clock 3111T/C SNP

Purohit, Kush (2014) Investigating the functional implications of the Clock 3111T/C SNP. Undergraduate Thesis, University of Pittsburgh. (Unpublished)

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Abstract

Introduction: Bipolar disorder (BD) is a debilitating mental illness proven to be very difficult to treat. By studying the molecular mechanisms that underlie BD, we can learn how to improve treatments. The CLOCK protein is a key transcription factor involved in the persistence of circadian rhythms. Studies have found that manipulations of the Clock gene are sufficient to produce manic-like behavior in mice. The Clock 3111T/C single-nucleotide polymorphism (SNP) is a variation of the human Clock gene that is associated with increased frequency of mania in BD patients. In this study, we sought to examine the functional implications of the Clock 3111T/C SNP on Clock and Per2 expression over 24 hours.
Methods and Materials: Plasmid construction: The human Clock gene was cloned and site-directed mutagenesis was performed to produce the 3111T and 3111C versions of the gene. An Npas2 shRNA was also constructed in order to knockdown Npas2 expression, which has been shown to be significantly upregulated in Clock KO MEFs. MEFs: Mouse embryonic fibroblasts (MEFs) were collected from Clock Knockout (KO) mice. Clock KO MEFs were used to avoid confounds of endogenous Clock expression. Transfections: MEFs were transfected with either the Clock T or C constructs, in addition with an Npas2 shRNA. Quantitative PCR: RNA from transfected MEFs was isolated, and then reverse-transcribed to cDNA. Quantitative polymerase chain reaction (qPCR) was performed over a 24 hour period.
Results: Quantitative PCR revealed significantly increased levels of Clock and Per2 mRNA over a 24-hour time course in MEFs expressing the 3111C SNP, as compared with 3111T.
Conclusions: The CLOCK protein controls expression of genes beyond the circadian clock. These include dopamine regulators, which are known to be involved in decreased depression-like behaviors and increased impulsivity/drug intake. From this, it is clear that altered Clock expression may have tremendous implications for a variety of diseases, including BD.


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Details

Item Type: University of Pittsburgh ETD
Status: Unpublished
Creators/Authors:
CreatorsEmailPitt UsernameORCID
Purohit, Kushkush.purohit.pitt@gmail.com
ETD Committee:
TitleMemberEmail AddressPitt UsernameORCID
Committee ChairMcClung, Colleen A.mcclungc@pitt.eduMCCLUNGC
Committee MemberMoghaddam, Bitabita@pitt.eduBITA
Committee MemberCard, J Patrickcard@pitt.eduCARD
Committee MemberMcManus, C. Joelmcmanus@andrew.cmu.edu
Date: 24 April 2014
Date Type: Publication
Defense Date: 25 March 2014
Approval Date: 24 April 2014
Submission Date: 28 March 2014
Access Restriction: 5 year -- Restrict access to University of Pittsburgh for a period of 5 years.
Number of Pages: 31
Institution: University of Pittsburgh
Schools and Programs: Dietrich School of Arts and Sciences > Neuroscience
University Honors College
Degree: BPhil - Bachelor of Philosophy
Thesis Type: Undergraduate Thesis
Refereed: Yes
Uncontrolled Keywords: Clock, gene, genetics, human, SNP, single nucleotide polymorphism, 3111T/C, 3111T, 3111C, mRNA, degradation, qPCR, gene expression, Per2, protein, circadian, rhythms
Date Deposited: 24 Apr 2014 13:48
Last Modified: 24 Apr 2019 05:15
URI: http://d-scholarship.pitt.edu/id/eprint/20874

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