Publications by authors named "Marie-Line Faucillion"

The Borrelia consists of three groups of species, those of the Lyme borreliosis (LB) group, also known as B. burgdorferi sensu lato (s.l.

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The steady state levels of RNAs, often referred to as expression levels, result from a well-balanced combination of RNA transcription and decay. Alterations in RNA levels will therefore result from tight regulation of transcription rates, decay rates or both. Here, we explore the role of RNA stability in achieving balanced gene expression and present genome-wide RNA stabilities in Drosophila melanogaster male and female cells as well as male cells depleted of proteins essential for dosage compensation.

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Article Synopsis
  • The male-specific lethal (MSL) complex in Drosophila melanogaster is crucial for balancing gene expression on the male X-chromosome, consisting of MSL proteins and two long noncoding RNAs, roX1 and roX2.
  • Research shows that while roX1 and roX2 seem redundant, they have distinct roles; roX1 is vital for maintaining gene expression, while roX2 may influence male-biased gene activation independently.
  • Deleting both roX genes leads to significant gene expression reduction, indicating that effective dosage compensation may involve complex regulatory dynamics and potential evolutionary adaptations in how sex chromosomes manage gene expression.
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  • Mammalian sex chromosomes evolved from the degradation of one half of a pair of ancient autosomes, leading to an imbalance in gene expression that is partially corrected by increasing the activity of the X-chromosome.
  • Research found that X-chromosome gene transcripts have longer half-lives and higher ribosome density compared to autosomal transcripts in both human and mouse cells, indicating that they are more stable and translated at a higher rate.
  • These findings support the idea that differences in mRNA stability and translation between sex and autosomal chromosomes help maintain a balance in gene expression, contributing to a well-established mechanism for dosage compensation in mammals.
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In Drosophila melanogaster, two chromosome-specific targeting and regulatory systems have been described. The male-specific lethal (MSL) complex supports dosage compensation by stimulating gene expression from the male X-chromosome, and the protein Painting of fourth (POF) specifically targets and stimulates expression from the heterochromatic 4(th) chromosome. The targeting sites of both systems are well characterized, but the principles underlying the targeting mechanisms have remained elusive.

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