Sean D. Gallaher

The paper revises the model of the Chlamydomonas reinhardtii mitochondrial genome by identifying structural heteroplasmy and a recombination-dependent replication mechanism.

The paper introduces a 'mono-mix' strategy to improve proteomic analysis of cross-kingdom microbial symbiosis by addressing detection biases in coculture.

This study investigates overflow metabolism in Chromochloris zofingiensis under different nutrient and light conditions using metabolic flux analysis and transcriptomics.

This study presents a diploid genome assembly and genetic toolkit for Auxenochlorella, revealing evolutionary forces like mitotic recombination and loss-of-heterozygosity, and demonstrating its utility for research and bioengineering.

This study shows Chlamydomonas reinhardtii can rapidly reprogram its photoprotective strategies in response to changes in diurnal light intensity, with LL-acclimated cells recovering faster than HL-acclimated cells.

The paper shows Fe starvation in green algae leads to a second LHCI tetramer associated with PSI, similar to cyanobacteria's isiA antenna ring.

The paper identifies leaky ribosomal scanning as the mechanism enabling tunable translation of bicistronic ORFs in green algae through bioinformatic and in vivo analyses.

The paper identifies a mutation in CEHC1, which encodes FBXO3, leading to normoxic expression of HYDA genes in Chlamydomonas reinhardtii by stabilizing CRR1.

The paper analyzes how Chlamydomonas adapts its gene expression and proteomic profiles to different light conditions, revealing constitutive phenotypes that persist through the night.

This study examines how Chlamydomonas cells adjust to Fe-free conditions, showing rapid transcriptomic changes and slower metabolic shifts.

The paper analyzes two extremophilic algae to understand their iron management strategies, identifying novel iron-uptake proteins and adaptive mechanisms that enable survival in low-iron environments.

The paper presents version 6 of the Chlamydomonas reinhardtii reference genome, improving assembly quality and revealing structural mutations in laboratory strains.