Mapping deep evolutionary divergences in cellular models of stress response

NIH RePORTER · NIH · R01 · $87,845 · view on reporter.nih.gov ↗

Abstract

SUMMARY Understanding how nature builds new traits is a fundamental goal of evolutionary genetics. Unbiased experimental dissection of trait variation from the wild has to date used linkage or association mapping, which are suitable only for crosses between compatible individuals of a given species. The parent R01 for this supplement makes use of a method from our group called RH-seq, which enables the genetic mapping of natural trait variation between reproductively isolated species. One aim of the parent R01 focuses on evolutionary and biophysical mechanisms of a model trait, high-temperature growth in Saccharomyces yeast. A second aim of the parent R01 applies RH-seq to a cell-autonomous mouse phenotype called cellular senescence. In this supplement, we propose to provide training to Abel Duarte, a Ph.D. student in the Microbiology graduate program at UC Berkeley, to extend our analyses to the budding yeast Kluyveromyces. In these distant relatives of Saccharomyces, we have found a suite of stress-resistance traits distinguishing one species, K. marxianus, from the rest of the clade. We propose to use RH-seq and other omics approaches to dissect this trait syndrome. Since K. marxianus diverged 20 million years ago from its closest relative, the clade affords us the opportunity to study trait evolution over a far deeper divergence than we or others have achieved in any quantitative-genetic mapping work to date. This project will involve computational data analysis, applied statistics, and molecular evolution tests as well as experimental genomics and molecular biology. It represents an excellent training opportunity for Abel to master computational/quantitative skills, which he has set out in his Individual Development Plan as a major training goal. As such, funding this supplement will support Abel’s development as a quantitative genomic scientist; and since Abel is of Mexican descent and the first in his family to have gone to college, as he harnesses our training to complete his Ph.D. and move on to a career in biomedical research, he will contribute to the diversity of the workforce.

Key facts

NIH application ID
10699808
Project number
3R01GM120430-06S1
Recipient
UNIVERSITY OF CALIFORNIA BERKELEY
Principal Investigator
Rachel Beth Brem
Activity code
R01
Funding institute
NIH
Fiscal year
2023
Award amount
$87,845
Award type
3
Project period
2017-05-15 → 2026-02-28