Publications by authors named "Alexandra L Mattei"

The blueprint of the mammalian body plan is laid out during gastrulation, when a trilaminar embryo is formed. This process entails a burst of proliferation, the ingression of embryonic epiblast cells at the primitive streak, and their priming toward primitive streak fates. How these different events are coordinated remains unknown.

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Regulatory landscapes drive complex developmental gene expression, but it remains unclear how their integrity is maintained when incorporating novel genes and functions during evolution. Here, we investigated how a placental mammal-specific gene, Zfp42, emerged in an ancient vertebrate topologically associated domain (TAD) without adopting or disrupting the conserved expression of its gene, Fat1. In ESCs, physical TAD partitioning separates Zfp42 and Fat1 with distinct local enhancers that drive their independent expression.

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Article Synopsis
  • DNA methylation plays a key role in cell development and stability, but cancer often disrupts this process, showing a global loss of methylation and increased CpG island hypermethylation.
  • Acute lymphoblastic leukemia (ALL), the most common childhood cancer, presents unique methylation patterns, revealing hypermethylation of CpG islands without the typical global loss seen in other cancers.
  • Whole-genome analysis indicates significant variability in CpG island hypermethylation among ALL patients, influenced by specific genes (TET2 and DNMT3B), highlighting a distinct regulatory mechanism for methylation in leukemia.
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In 1925, 5-methylcytosine was first reported in bacteria. However, its biological importance was not intuitive for several decades. After this initial lag, the ubiquitous presence of this methylated base emerged across all domains of life and revealed a range of essential biological functions.

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Article Synopsis
  • DNA methylation is essential during development for repressing retrotransposons, with key enzymes being Dnmt1 for maintenance and Dnmt3a/3b for de novo activity.
  • Research shows that Dnmt1 also has de novo methylation capabilities and specifically targets retrotransposons, which was analyzed using advanced sequencing techniques in methylation-depleted mouse embryonic stem cells.
  • The activity of Dnmt1 is dependent on Uhrf1, and its recruitment overlaps with certain epigenetic markers, indicating its dual role in both maintaining and initiating DNA methylation for stable repression during development.*
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Mammalian cells stably maintain high levels of DNA methylation despite expressing both positive (DNMT3A/B) and negative (TET1-3) regulators. Here, we analyzed the independent and combined effects of these regulators on the DNA methylation landscape using a panel of knockout human embryonic stem cell (ESC) lines. The greatest impact on global methylation levels was observed in DNMT3-deficient cells, including reproducible focal demethylation at thousands of normally methylated loci.

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In normal mammalian development cytosine methylation is essential and is directed to specific regions of the genome. Despite notable advances through mapping its genome-wide distribution, studying the direct contribution of DNA methylation to gene and genome regulation has been limited by the lack of tools for its precise manipulation. Thus, combining the targeting capability of the CRISPR-Cas9 system with an epigenetic modifier has attracted interest in the scientific community.

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Within the mated reproductive tracts of females of many taxa, seminal fluid proteins (SFPs) coagulate into a structure known as the mating plug (MP). MPs have diverse roles, including preventing female remating, altering female receptivity postmating, and being necessary for mated females to successfully store sperm. The Drosophila melanogaster MP, which is maintained in the mated female for several hours postmating, is comprised of a posterior MP (PMP) that forms quickly after mating begins and an anterior MP (AMP) that forms later.

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Physiological changes in females during and after mating are triggered by seminal fluid components in conjunction with female-derived molecules. In insects, these changes include increased egg production, storage of sperm, and changes in muscle contraction within the reproductive tract (RT). Such postmating changes have been studied in dissected RT tissues, but understanding their coordination in vivo requires a holistic view of the tissues and their interrelationships.

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The storage of sperm in mated females is important for efficient reproduction. After sperm are transferred to females during mating, they need to reach and enter into the site(s) of storage, be maintained viably within storage, and ultimately be released from storage to fertilize eggs. Perturbation of these events can have drastic consequences on fertility.

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