We have studied protein synthesis in the viable hybrid Xenopus laevis (female) X Xenopus borealis (male) using 2D gel electrophoresis. Fourteen borealis-specific proteins were studied. Two of these proteins appeared by the gastrula stage, five in the gastrula and the rest later. Where homologous laevis proteins were tentatively identified, androgenetic haploid hybrids were used to study whether the protein was encoded by stored maternal mRNA, and how long this mRNA persisted. The two proteins appearing in blastulae were probably initially coded by stored maternal mRNA. This was not detectable by the tailbud-tadpole stage, and presumably had been destroyed.

Download full-text PDF

Source

Publication Analysis

Top Keywords

xenopus laevis
8
xenopus borealis
8
stored maternal
8
maternal mrna
8
paternal gene
4
gene expression
4
expression developing
4
developing hybrid
4
hybrid embryos
4
xenopus
4

Similar Publications

Large vertebrate genomes duplicate by activating tens of thousands of DNA replication origins, irregularly spaced along the genome. The spatial and temporal regulation of the replication process is not yet fully understood. To investigate the DNA replication dynamics, we developed a methodology called RepliCorr, which uses the spatial correlation between replication patterns observed on stretched single-molecule DNA obtained by either DNA combing or high-throughput optical mapping.

View Article and Find Full Text PDF

Progesterone induces meiosis through two obligate co-receptors with PLA2 activity.

Elife

January 2025

Calcium Signaling Group, Research Department, Weill Cornell Medicine Qatar, Education City, Qatar Foundation, Doha, Qatar.

The steroid hormone progesterone (P4) regulates multiple aspects of reproductive and metabolic physiology. Classical P4 signaling operates through nuclear receptors that regulate transcription. In addition, P4 signals through membrane P4 receptors (mPRs) in a rapid nongenomic modality.

View Article and Find Full Text PDF

Animal models of kabuki syndrome and their applicability to novel drug discovery.

Expert Opin Drug Discov

January 2025

Division of Genetics and Genomics, Department of Pediatrics, Boston Children's Hospital, Boston, MA, USA.

Introduction: Kabuki Syndrome (KS) is a rare genetic disorder characterized by distinctive facial features, intellectual disability, and multiple congenital anomalies. It is caused by pathogenic variants in the and genes. Despite its significant disease burden, there are currently no approved therapies for KS, highlighting the need for advanced research and therapeutic development.

View Article and Find Full Text PDF

The amphibian metamorphosis assay (AMA) is an in vivo screen to assess potential interactions of chemicals with the amphibian thyroid system. Tadpoles are exposed for 21-days, then assessed for development and growth after 7 days and at test termination. This paper presents data from studies performed to satisfy test orders from the US EPA's Endocrine Disruptor Screening Program.

View Article and Find Full Text PDF

The brain and spinal cord originate from a neural tube that is preceded by a flat structure known as the neural plate during early embryogenesis. In humans, failure of the neural plate to convert into a tube by the fourth week of pregnancy leads to neural tube defects (NTDs), birth defects with serious neurological consequences. The signaling mechanisms governing the process of neural tube morphogenesis are unclear.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!