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New research shows how genes are turned on and off

New research shows how genes are turned on and off
Written by adrina

Genes & Development (2022). DOI: 10.1101/gad.350026.122″ width=”800″ height=”530″/>
Protein architectures of constitutive and inducible (RP, induced, primed, and state-specific) promoters. Composite diagrams of chromatin immunoprecipitation exonuclease (ChIP-exo) tag 5′ ends (exonuclease stop sites as shown) for 70 representative promoter/gene-associated proteins (out of 400) are shown around the indicated X-axis Reference point (UAS, Sua7 or +1 nuc) within each promoter class (rows of panels). Each target protein in a vertical column is defined by a color, the legend of which is at the bottom. Selected complexes represented by a protein are highlighted in specific boxes. See Materials and Methods for details. X-axis intervals are oriented so that transcription progresses to the right. UAS corresponds to an ssTF binding site or the equivalent distance upstream (150 bp) of a transcription start site (TSS) when no UAS was present. Sua7 (TFIIB) corresponds to the Sua7 ChExMix peak closest to an annotated TSS and is essentially the PIC position. +1 nuc is the downstream nucleosome midpoint closest to a TSS. Aligning to these reference features provided high position resolution. Comparative strand data is inverted. “N” denotes the number of class memberships. The occupancy scale on the Y-axis is the same for a given target across the different promoter classes and is therefore comparable (Analysis ID: CM701-CM707). Recognition: Genes & Development (2022). DOI: 10.1101/gad.350026.122

Yeast, that simple organism essential to making beer and bread, researchers at Cornell University have uncovered a key mechanism for controlling genes.

Gene transcription — the sophisticated process our cells use to read genetic information stored in DNA — has long been thought to be activated when specific regulatory factors target specific DNA sequences. In new research, a team of Cornell scientists discovered that certain genes have their transcription-regulating factors and cofactors already present but in a latent state. With the appropriate signals, these “balanced” genes become highly active.

Using CRISPR techniques, the researchers removed parts of the yeast transcription machinery to systematically study their role in regulating genes. Yeast and humans share much of the same molecular machinery to regulate their genes, so yeast provides an excellent model for understanding gene regulation in humans.

“It’s like playing Jenga, where you remove a block from a tower of blocks and see if the whole thing collapses. This is how we learn how protein machines work in cells,” said B. Franklin Pugh, professor of molecular biology and genetics and corresponding author of the study.

“The value of readiness is that certain genes, like environmental response genes, can respond quickly to a changing environment, such as when yeast encounters bread sugar and metabolizes it, which causes bread dough to rise,” Pugh said.

“Building on years of existing research and combining it with modern and elegant genomics tools has helped us to fill gaps in current knowledge and make new discoveries,” said Chitvan Mittal, first author and research associate at the Baker Institute for Animal Health in the Faculty of Veterinary Medicine.

The study was published in Genes & Development.


Yeast epigenome map reveals details of gene regulation


More information:
Chitvan Mittal et al., An integrated SAGA and TFIID-PIC assembly pathway selective for primed and induced promoters, Genes & Development (2022). DOI: 10.1101/gad.350026.122

Provided by Cornell University

Citation: New Research Reveals How Genes Are Turned On and Off (2022 October 27) Retrieved October 27, 2022 from https://phys.org/news/2022-10-reveals-genes.html

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