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Biology subjects

Parker, K. J.

Publications and source records attributed to Parker, K. J..

2 recordsLinked to original sources

Stereotypy is strongly linked to multiple biomarkers of oxidative stress--a potential common etiology for Abnormal Repetitive Behaviors

Spontaneous stereotypies (abnormal, repetitive, and seemingly goal-less behaviors) in captive animals resemble stereotypies documented in patients with neurodevelopmental disorders, including evidence of homologous cortico-striatal dysfunction and shared behavioral deficits. While environmental risk factors for stereotypies are well documented, their developmental pathophysiology remains unclear. However, as previously found for compulsive behavior, there is growing evidence that REDOX imbalance may be linked to stereotypy. To examine the nature of this relationship, we first tested whether plasma glutathione level, the gold-standard biomarker of REDOX imbalance, is predictive of stereotypy severity in N=19 C57BL/6 mice. After confirming the presence of this relationship, we used a proteomics approach (Olink) to identify a broader biomarker profile of dysfunction. We found expression of 9 proteins to correlate with plasma glutathione level, and expression of 15 proteins to correlate with stereotypy severity. A subset of these proteins additionally correlated with stereotypy severity in a validation cohort of CD1 mice (N=28). Further supporting a role for REDOX imbalance in the developmental pathophysiology of stereotypies, the identified proteins were associated with REDOX physiology, dopamine physiology, and stereotypy-presenting human neurodevelopmental disorders. These data suggest REDOX imbalance may contribute to the developmental pathophysiology of abnormal repetitive behaviors and highlight promising novel targets for intervention.

animal behavior and cognition↗

Haplotype-phased Callithrix jacchus embryonic stem cell line for genome editing using CRISPR/Cas9

Due to anatomical and physiological similarities to humans, the common marmoset (Callithrix jacchus) is an ideal organism for the study human diseases. Researchers are currently leveraging genome-editing technologies such as CRISPR/Cas9 to genetically engineer marmosets for the in vivo biomedical modeling of human neuropsychiatric and neurodegenerative diseases. The genome characterization of these cell lines greatly reinforces these transgenic efforts. It also provides the genomic contexts required for the accurate interpretation of functional genomics data. We performed haplotype-resolved whole-genome characterization for marmoset ESC line cj367 from the Wisconsin National Primate Research Center. This is the first haplotype-resolved analysis of a marmoset genome and the first whole-genome characterization of any marmoset ESC line. We identified and phased single-nucleotide variants (SNVs) and Indels across the genome. By leveraging this haplotype information, we then compiled a list of cj367 ESC allele-specific CRISPR targeting sites. Furthermore, we demonstrated successful Cas9 Endonuclease Dead (dCas9) expression and targeted localization in cj367 as well as sustained pluripotency after dCas9 transfection by teratoma assay. Lastly, we show that these ESCs can be directly induced into functional neurons in a rapid, single-step process. Our study provides a valuable set of genomic resources for primate transgenics in this post-genome era.

genetics↗