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FLC, which encodes the main repressor of flowering in Arabidopsis has become a model gene in the study of chromatin regulation [28], [44], [47].
To understand the evolution and dynamics of mitochondrial introns in fungi, we decided to determine the sequence and molecular organization of the commonly used cox1 model gene in the most widely cultivated mushroom in the world: Agaricus bisporus.
We therefore used a T-DNA insertion line (SALK_143190) to tag a mitochondrial model gene in the chromosome 2 cluster, and to sequence the nuclear copy of the gene.
In conclusion, the analysis of histone modifications and promoter activity under specific growth conditions allowed for the uncoupling of core promoter acetylation and transcription on a model gene in maize.
In addition, the study of histone modifications around this model gene in the roots revealed that the distal regulatory region was rich in H3K27me3 but that its abundance did not change as a consequence of stress.
In addition, to test the hypothesis of a link between epigenetics modifications and the adaptation of crop plants to abiotic stress, we exhaustively explored the cytosine methylation status in leaf Asr1 DNA, a model gene in our system, resulting from water-deficit stress conditions imposed on tomato plants.
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Expression patterns of ASD model genes in cerebellum.
In this model, gene alleles in the population are partially adapted to perform a new function but not efficiently.
Instead, we indirectly model gene duplications in two ways.
MaSigPro applies two generalized linear regression steps to model gene expression in time series expression data.
Although we did not detect a target gene in the 3 11 translocation in our model, genes involved in cell transformation are likely to be located in this region [27] [29].
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