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June 27, 2025

Scientists reveal how diverse cell types are produced in developing embryos

A developing mouse embryo expresses different genes (green, magenta, cyan) from head to tail, to generate different parts of the body. Credit: Irene Amblard, Development & Transcriptional Control Group, MRC Laboratory of Medical Sciences
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A developing mouse embryo expresses different genes (green, magenta, cyan) from head to tail, to generate different parts of the body. Credit: Irene Amblard, Development & Transcriptional Control Group, MRC Laboratory of Medical Sciences

A team of scientists at the MRC Laboratory of Medical Sciences (LMS) has uncovered a previously unknown mechanism that controls how genes are switched "on" and "off" during embryonic development. Their study sheds light on how diverse cell types are produced in developing embryos.

The research, in Developmental Cell, was led by Dr. Irène Amblard and Dr. Vicki Metzis from the Development and Transcriptional Control group, in collaboration with LMS facilities and the Chromatin and Development and Computational Regulatory Genomics groups.

All cells contain the same DNA but must turn '"on" and "off"—a process known as gene expression—to create different body parts. The cells in your eyes and arms harbor the same genes but "express" them differently to become each body part.

The work focused on the gene Cdx2. The duration of Cdx2 expression helps to determine where and when a cell produces spinal cord progenitors. The researchers wanted to understand what processes control this brief window.

The team discovered a DNA element they termed an "attenuator," which reduces gene expression in a time and cell type-specific manner—unlike enhancers or silencers, other types of DNA elements that broadly switch genes on or off.

By altering this element, they could tune how long or how strongly Cdx2 was expressed, effectively acting like a "genetic dimmer switch." Disrupting the "switch" in mouse embryos also confirmed its essential role in shaping the developing body plan.

This breakthrough paves the way towards programmable gene expression, offering the ability to precisely control gene activity in space and time. The findings not only deepen our understanding of developmental biology but may inform new .

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Such approaches could one day enable treatments that selectively adjust gene expression in specific tissues, with implications for diseases caused by gene misregulation.

Vicki emphasized the potential, saying, "We're excited because previous research suggests that our genome may harbor many different types of elements that finely tune gene expression, but they've not been easy to identify. If we can address this challenge, this holds enormous potential for unlocking new ways to treat diseases by fine-tuning where and when it's needed."

The study adds to a growing body of work exploring how non-coding DNA governs —an area with profound implications for medicine, from designing new gene therapies to improving treatments.

More information: A dual enhancer-attenuator element ensures transient Cdx2 expression during mouse posterior body formation, Developmental Cell (2025). .

Journal information: Developmental Cell

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A newly identified DNA element, termed an "attenuator," modulates gene expression duration and intensity in a cell type- and time-specific manner during embryonic development. This mechanism, distinct from enhancers or silencers, is essential for proper body plan formation and offers potential for precise, programmable control of gene activity, with implications for therapeutic strategies targeting gene misregulation.

This summary was automatically generated using LLM.