Marzie Rasekh Successfully Defends Her Thesis
Congratulations to Marzie Rasekh on the successful defense of their thesis, "Characterizing VNTRS in Human Populations" Great job Marzie!
To learn more about Marzie's thesis, read their abstract below:
Over half the human genome consists of repetitive sequences. One major class is the tandem repeats (TRs), which are defined by their location in the genome, repeat unit, and copy number. TRs loci which exhibit variant copy numbers are called Variable Number Tandem Repeats (VNTRs). High VNTR mutation rates of approximately 10-4 per generation make them suitable for forensic studies, and of interest for potential roles in gene regulation and disease. TRs are generally divided into three classes: 1) microsatellites or short tandem repeats (STRs) with patterns <7 bp; 2) minisatellites with patterns of seven to hundreds of base pairs; and 3) macrosatellites with patterns of >100 bp. To date, mini- and macrosatellites have been poorly characterized, mainly due to a lack of computational tools. In this thesis, I utilize a tool, VNTRseek, to identify human minisatellite VNTRs using short read sequencing data from nearly 2,800 individuals and developed a new computational tool, MaSUD, to identify human macrosatellite VNTRs using data from 2,504 individuals. MaSUD is the first high-throughput tool to genotype macrosatellites using short reads.
I identified over 35,000 minisatellite VNTRs and over 4,000 macrosatellite VNTRs, most previously unknown. A small subset in each VNTR class was validated experimentally and in silico. The detected VNTRs were further studied for their effects on gene expression, ability to distinguish human populations, and functional enrichment. Unlike STRs, mini- and macrosatellite VNTRs are enriched in regions with functional importance, e.g., introns, promoters, and transcription factor binding sites. A study of VNTRs across 26 populations shows that minisatellite VNTR genotypescan be used to predict super-populations with >90% accuracy. In addition, genotypes for 195 minisatellite VNTRs and 24 macrosatellite VNTRs were shown to be associated with differential expression in nearby genes (eQTLs).
Finally, I developed a computational tool, mlZ, to infer undetected VNTR alleles and to detect false positive predictions. mlZ is applicable to other tools that use read support for predicting short variants.
Overall, these studies provide the most comprehensive analysis of mini- and macrosatellites in human populations and will facilitate the application of VNTRs for clinical purposes.
Major Professor: Gary Benson