4.6 Article

cgaTOH: Extended Approach for Identifying Tracts of Homozygosity

Journal

PLOS ONE
Volume 8, Issue 3, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0057772

Keywords

-

Ask authors/readers for more resources

Identification of disease variants via homozygosity mapping and investigation of the effects of genome-wide homozygosity regions on traits of biomedical importance have been widely applied recently. Nonetheless, the existing methods and algorithms to identify long tracts of homozygosity (TOH) are not able to provide efficient and rigorous regions for further downstream association investigation. We expanded current methods to identify TOHs by defining surrogate-TOH'', a region covering a cluster of TOHs with specific characteristics. Our defined surrogate-TOH includes cTOH, viz a common TOH region where at least ten TOHs present; gTOH, whereby a group of highly overlapping TOHs share proximal boundaries; and aTOH, which are allelically-matched TOHs. Searching for gTOH and aTOH was based on a repeated binary spectral clustering algorithm, where a hierarchy of clusters is created and represented by a TOH cluster tree. Based on the proposed method of identifying different species of surrogate-TOH, our cgaTOH software was developed. The software provides an intuitive and interactive visualization tool for better investigation of the high-throughput output with special interactive navigation rings, which will find its applicability in both conventional association studies and more sophisticated downstream analyses. NCBI genome map viewer is incorporated into the system. Moreover, we discuss the choice of implementing appropriate empirical ranges of critical parameters by applying to disease models. This method identifies various patterned clusters of SNPs demonstrating extended homozygosity, thus one can observe different aspects of the multi-faceted characteristics of TOHs.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

Article Oncology

One Size Does Not Fit All: Breast Cancer in Young Women

Lamis Yehia, Charis Eng

Summary: The study of characteristics of breast cancer in young women has important implications for personalized genomics-driven management.

CLINICAL CANCER RESEARCH (2022)

Article Oncology

Fecal microbiota of adolescent and young adult cancer survivors and metabolic syndrome: an exploratory study

Seth J. Rotz, Naseer Sangwan, Matthew Nagy, Alice Tzeng, Margaret Jia, Maria Moncaliano, Navneet S. Majhail, Charis Eng

Summary: The intestinal microbiome diversity of long-term survivors of pediatric cancer is reduced, and radiation therapy may further decrease the diversity. The microbiome composition is associated with metabolic syndrome, obesity, and chronic inflammation in these survivors.

PEDIATRIC HEMATOLOGY AND ONCOLOGY (2022)

Article Genetics & Heredity

Distinct metabolic profiles associated with autism spectrum disorder versus cancer in individuals with germline PTEN mutations

Lamis Yehia, Ying Ni, Tammy Sadler, Thomas W. Frazier, Charis Eng

Summary: A metabolomics study on PHTS individuals with ASD/DD, cancer, or both phenotypes found differentially abundant metabolites and distinct metabolic phenotypes, indicating that metabolites may enable more accurate risk predictions and prevention in individual PHTS patients at highest risk.

NPJ GENOMIC MEDICINE (2022)

Article Genetics & Heredity

Exome sequencing reveals a distinct somatic genomic landscape in breast cancer from women with germline PTEN variants

Takae Brewer, Lamis Yehia, Peter Bazeley, Charis Eng

Summary: Findings from this study suggest that breast cancers arising from germline PTEN variants have distinct genomic characteristics compared to sporadic breast cancers, including distinct somatic mutational landscape, increased genomic instability, and higher frequency of somatic PTEN variants. These findings have important implications for the personalized management of PTEN-related breast cancers.

AMERICAN JOURNAL OF HUMAN GENETICS (2022)

Article Endocrinology & Metabolism

Development and Progression of Thyroid Disease in PTEN Hamartoma Tumor Syndrome: Refined Surveillance Recommendations

Gilman Plitt, Takae Brewer, Lamis Yehia, Judy Jin, Joyce Shin, Charis Eng

Summary: This study investigated the time to develop thyroid nodules and thyroid cancer in PHTS patients. The findings suggest that PHTS patients without nodules on ultrasound can extend surveillance intervals to 3-5 years, while patients with clinically nonactionable nodules can extend surveillance intervals to 2-3 years, instead of the current recommendation of annual ultrasounds.

THYROID (2022)

Article Chemistry, Medicinal

Structural and Dynamic Effects of PTEN C-Terminal Tail Phosphorylation

Iris N. Smith, Jennifer E. Dawson, James Krieger, Stetson Thacker, Ivet Bahar, Charis Eng

Summary: The study reveals the mechanism of CTT phosphorylation dynamics in PTEN and identifies potential druggable allosteric sites in a previously believed clinically undruggable protein.

JOURNAL OF CHEMICAL INFORMATION AND MODELING (2022)

Article Gastroenterology & Hepatology

Clinical Spectrum and Science Behind the Hamartomatous Polyposis Syndromes

Lamis Yehia, Brandie Heald, Charis Eng

Summary: Hamartomatous polyposis syndromes are a group of clinically distinct disorders characterized by hamartomatous polyps in the gastrointestinal tract. These syndromes include juvenile polyposis syndrome, Peutz-Jeghers syndrome, and PTEN hamartoma tumor syndrome. Differentiating histologically between the polyps in each syndrome is challenging. Additionally, these syndromes are associated with increased risks of gene-specific and organ-specific cancers. Germline pathogenic variants can be identified and facilitate molecular diagnosis and gene-enabled management. Timely recognition enables presymptomatic cancer surveillance and management, although there are currently no standard agents for prevention.

GASTROENTEROLOGY (2023)

Article Chemistry, Physical

Comparative Protein Structural Network Analysis Reveals C-Terminal Tail Phosphorylation Structural Communication Fingerprint in PTEN-Associated Mutations in Autism and Cancer

Iris N. Smith, Jennifer E. Dawson, Charis Eng

Summary: PTEN is a key regulator of the PI3K/AKT/mTOR signaling pathway, and its phosphorylation affects its tumor suppressor function. Mutations in PTEN are associated with PTEN hamartoma tumor syndrome and autism spectrum disorder. This study used a comparative protein structure network approach to investigate the conformational dynamics induced by PTEN phosphorylation and identified differences between PTEN-ASD and PTEN-cancer phenotypes. The findings suggest that CTT phosphorylation affects the flexibility, inter-residue contacts, and allosteric communication patterns of PTEN.

JOURNAL OF PHYSICAL CHEMISTRY B (2023)

Article Genetics & Heredity

Brain single cell transcriptomic profiles in episodic memory phenotypes associated with temporal lobe epilepsy

Robyn M. Busch, Lamis Yehia, Bo Hu, Melissa Goldman, Bruce P. Hermann, Imad M. Najm, Steven A. McCarroll, Charis Eng

Summary: This study investigated the differences in cellular heterogeneity among patients with temporal lobe epilepsy (TLE) with or without impairment in verbal episodic memory using single-nucleus RNA sequencing technology. The study found significant cell heterogeneity between memory phenotypes and identified numerous differentially expressed genes across all brain cell types. The most notable differences were observed in glutamatergic and GABAergic neurons, which are associated with processes essential for episodic memory formation such as long-term potentiation, long-term depression, and MAPK signaling.

NPJ GENOMIC MEDICINE (2022)

Editorial Material Oncology

Two's Company, Three's a Crowd: Rb1/Trp53/Pten Trifecta and Lung Cancer Molecular and Histopathologic Heterogeneity

Lamis Yehia, Maria Laura Centomo, Pier Paolo Pandol, Charis Eng

JOURNAL OF THORACIC ONCOLOGY (2023)

Article Multidisciplinary Sciences

Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary disease

Shyam K. Poudel, Roshan Padmanabhan, Heloni Dave, Kathryn Guinta, Tyler Stevens, Madhusudhan R. Sanaka, Prabhleen Chahal, Davendra P. S. Sohal, Alok A. Khorana, Charis Eng

Summary: This study aimed to find malignancy-related microbiomic fingerprints in bile samples from patients with pancreaticobiliary malignancies. The results showed that both benign and malignant pancreaticobiliary diseases have distinct microbiomic compositions, and the relative abundance of certain bacteria varies between different types of pancreaticobiliary malignancies.

PLOS ONE (2023)

Article Biochemistry & Molecular Biology

Differential cell cycle checkpoint evasion by PTEN germline mutations associated with dichotomous phenotypes of cancer versus autism spectrum disorder

Masahiro Hitomi, Juan Venegas, Shin Chung Kang, Charis Eng

Summary: Individuals with a PTEN germline mutation, known as PTEN hamartoma tumor syndrome (PHTS), exhibit a range of symptoms including hamartomas, predisposition to cancers, and autism spectrum disorder (ASD). The specific genotype-phenotype correlations of PTEN mutations are not yet well-established due to limited information on the impact of these mutations on PTEN function. To address this knowledge gap, the researchers compared the functional effects of two selected missense PTEN mutations, G132D and M134R, which are associated with distinct clinical phenotypes of ASD and thyroid cancer without ASD, respectively. The findings suggest that the ASD-associated G132D allele promotes genome instability by prematurely reentering the cell cycle with incomplete DNA repair.

ONCOGENE (2023)

Article Genetics & Heredity

Integrating somatic CNV and gene expression in breast cancers from women with PTEN hamartoma tumor syndrome

Takae Brewer, Lamis Yehia, Peter Bazeley, Charis Eng

Summary: This study revealed distinct somatic landscape features in breast cancers derived from germline PTEN variants, including unique copy number variations and transcriptomic signatures. The transcriptome data also identified a key pathway associated with tumorigenesis involving vitamin E degradation in patients with pathogenic germline PTEN variants.

NPJ GENOMIC MEDICINE (2023)

Article Genetics & Heredity

The mitochondrial genome as a modifier of autism versus cancer phenotypes in PTEN hamartoma tumor syndrome

Ruipeng Wei, Lamis Yehia, Ying Ni, Charis Eng

Summary: Cancer and autism spectrum disorder/developmental delay (ASD/DD) are common clinical phenotypes in individuals with germ-line PTEN variants (PTEN hamartoma tumor syndrome, PHTS). This study investigates the mitochondrial genome (mtDNA) in PHTS individuals and finds that mtDNA may act as a modifier of ASD/DD versus cancer in PHTS. The study shows that PHTS-onlyASD/DD has higher mtDNA copy number than PHTS-onlyCancer group and PHTS-neither group has higher mtDNA variant burden than PHTS-ASDCancer group.

HUMAN GENETICS AND GENOMICS ADVANCES (2023)

Article Clinical Neurology

Molecular and subregion mechanisms of episodic memory phenotypes in temporal lobe epilepsy

Robyn M. Busch, Lamis Yehia, Ingmar Bluemcke, Bo Hu, Richard Prayson, Bruce P. Hermann, Imad M. Najm, Charis Eng

Summary: Memory impairment in temporal lobe epilepsy is associated with molecular alterations within temporal lobe subregions that are independent from hippocampal cell loss, demographic variables, and disease characteristics. Each temporal subregion shows a unique molecular signature associated with memory impairment.

BRAIN COMMUNICATIONS (2022)

No Data Available