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Lachancea kluyveri

ABSTRACT: Petite-negative budding yeast (known as Lachancea kluyveri or Saccharomyces kluyveri) sequenced for comparative genomics studies

PROVIDER: PRJNA9594 | ENA |

REPOSITORIES: ENA

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			Action	DRS
		Other
	SRR11498251.fastq.gz	Fastqsanger.gz
	SRR11498252.fastq.gz	Fastqsanger.gz
	SRR11498253.fastq.gz	Fastqsanger.gz
	SRR11498254.fastq.gz	Fastqsanger.gz

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Iron-responsive genes in Lachancea kluyveri

Project description:To understand the iron-responsive gene expression in Lachancea kluyveri under high and low iron conditions, we perfomred the genome-wide gene expression profiling for the log-phase cells of Lachancea kluyveri wild type, sef1 deletion, aft1 deletion and sef1aft1 double deletion mutants under the YPD+400mM ferrous iron and YPD+ 200 mM BPS conditions.

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Sef1-dependent gene expression in Lachancea kluyveri

Project description:To understand the Sef1-dependent gene expression in Lachancea kluyveri under both fermentative and respiratory conditions, we perfomred the genome-wide gene expression profiling for the log-phase cells of Lachancea kluyveri wild type and sef1 deletion mutant under both YPD and YPGly conditions.

2019-04-26 | GSE130297 | GEO

Absence of chromosome axis proteins recruitment prevents meiotic recombination chromosome-wide in the budding yeast Lachancea kluyveri (Hi-C)

Project description:Absence of chromosome axis proteins recruitment prevents meiotic recombination chromosome-wide in the budding yeast Lachancea kluyveri

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Sef1-VP16 dependent gene expression in Lachancea kluyveri

Project description:To understand the highly active Sef1-VP16 dependent gene expression in Lachancea kluyveri under both fermentative and respiratory conditions, we perfomred the genome-wide gene expression profiling for the log-phase cells of Lachancea kluyveri wild type and SEF1-VP16 gain-of-function mutant under both YPD and YPGly conditions.

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Lachancea kluyveri (formerly Saccharomyces kluyveri); Growth on different nitrogen sources.

2013-06-21 | GSE48135 | GEO

Lachancea kluyveri

Project description:Lachancea kluyveri (formerly Saccharomyces kluyveri) Growth on different nitrogen sources.

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Selenite treatment of a Lachancea kluyveri wild type strain

Project description:In the frame of a multispecies project, Lachancea kluyveri cells were treated with 5 mM sodium selenite. Cells were collected 10, 20, 30, 40, 50, 60, 70 and 80 minutes after the treatment and their transcriptomes were compared to those of mock-treated cultures. Four independent biological replicates were performed.

2018-11-12 | E-MTAB-7046 | biostudies-arrayexpress

Lachancea kluyveri (formerly Saccharomyces kluyveri); Growth on different nitrogen sources.

Project description:Transcriptional profiling of the yeast Lachancea kluyveri when grown on minimal media with different compounds added as the sole nitrogen source. Cells grown on uracil, uridine, dihydrouracil and ammonia were profiled using cells grown on proline as the reference. Five conditions, of one was used as reference. Each grown in 4 parallell biological replicates, which were extracted, labeled and hybridized individually, except for the reference where the replicates were pooled. 1 technical replicate. Please note that raw data files for the following samples are not available; Skluy_uracil_rep2, Skluy_dihydrouracil_rep3, Skluy_uridine_rep4

2013-06-21 | E-GEOD-48135 | biostudies-arrayexpress

S-phase time-course of Lachancea kluyveri cells

Project description:Haploid cells of Lachancea kluyveri were arrested in G1 phase using Saccharomices cerevisiae alpha factor. After, release in a new media, cells go synchronously through S-phase. One sample is taken every five minutes. Microarrays are used to monitor the change of DNA copy number from 1 to 2, all along the genome during S-phase.

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Absence of chromosome axis proteins recruitment prevents meiotic recombination chromosome-wide in the budding yeast Lachancea kluyveri (CC-Seq)

Project description:Here we studied the budding yeast Lachancea kluyveri, a cousin of the model Saccharomyces cerevisiae, in order to try to understand the mechanism responsible for the absence of meiotic recombination on its almost entire sex chromosome (Brion et al. 2017). We performed meiotic DSB mapping using CC-seq (Gittens 2019). Briefly, we observed a distribution of meiotic DSBs mainly in gene promoters as in S. cerevisiae and a depletion within Lakl0C-left (the 1 Mb long domain on the sex chromosome with no meiotic recombination). Also, we noted a poor conservation of DSB hotspots strength between L. kluyveri and S. cerevisiae.

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