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Biology subjects

Yaakov, G.

Publications and source records attributed to Yaakov, G..

6 recordsLinked to original sources

Activator-binding domains are required but insufficient for Med15 recruitment to UAS, revealing a critical role for its disordered C-terminus in directing genome targeting

The Mediator complex is a conserved transcriptional coactivator that bridges transcription factors (TFs) with the core transcriptional machinery. In budding yeast, TFs recruit the Mediator to upstream activation sequences (UASs) by interacting with three activator-binding domains (ABDs) within the Med15 tail subunit. However, these ABD-TF interactions exhibit relatively low affinity, raising the question of whether they fully account for Med15 recruitment in vivo. Here, we address this question by combining genome-wide profiling with systematic mutational analysis. We demonstrate that while the three ABDs are collectively required for Med15 recruitment, they are not individually required and are not sufficient to specify the genomic binding pattern of Med15. Instead, removal of an intrinsically disordered C-terminal redistributes Med15 occupancy across UASs. Notably, C-terminal truncation alters Med15 binding even at TF-depleted regions, and these effects are recapitulated by deleting Med2 or Med3, which further stabilize TF-dependent recruitment. Together, these findings support a dual mechanism of Med15 UAS recruitment, whereby TF-ABD recruitment is directed and stabilized by C-terminal mediated interactions.

genomics↗

The molecular mechanism of on-demand sterol biosynthesis at organelle contact sites

Contact-sites are specialized zones of proximity between two organelles, essential for organelle communication and coordination. The formation of contacts between the Endoplasmic Reticulum (ER), and other organelles, relies on a unique membrane environment enriched in sterols. However, how these sterol-rich domains are formed and maintained had not been understood. We found that the yeast membrane protein Yet3, the homolog of human BAP31, is localized to multiple ER contact sites. We show that Yet3 interacts with all the enzymes of the post-squalene ergosterol biosynthesis pathway and recruits them to create sterol-rich domains. Increasing sterol levels at ER contacts causes its depletion from the plasma membrane leading to a compensatory reaction and altered cell metabolism. Our data shows that Yet3 provides on-demand sterols at contacts thus shaping organellar structure and function. A molecular understanding of this proteins functions gives new insights into the role of BAP31 in development and pathology.

cell biology↗

Histone exchange sensors reveal variant specific dynamics in mouse embryonic stem cells

Eviction of histones from nucleosomes and their exchange with newly synthesized or alternative variants is a central epigenetic determinant. Here, we define the genome-wide incorporation and exchange pattern of canonical and non-canonical histone variants in mouse embryonic stem cells by implementing a recently established, genetically encoded exchange sensor. While exchange of all measured variants scales with transcription, we describe variant-specific associations with transcription elongation and Polycomb binding. We found considerable exchange of H3.1 and H2B variants in heterochromatin and repeat elements, contrasting the stable incorporation and little exchange of H3.3 in these regions. This unexpected association between H3.3 incorporation and exchange of canonical variants is also evident in active promoters and enhancers, and further validated by reduced H3.1 dynamics following depletion of the HIRA H3.3-specific chaperone. The sensor system provides a powerful tool for studying regulation of histone dynamics toward understanding its role in shaping the epigenetic landscape in vivo.

genomics↗

Rtt109 promotes nucleosome replacement ahead of the replicating fork

DNA replication perturbs chromatin by triggering the eviction, replacement and incorporation of nucleosomes. How this dynamic is orchestrated in time and space is poorly understood. Here, we apply a recently established sensor for histone exchange to follow the time-resolved histone H3 exchange profile in budding yeast cells undergoing synchronous replication. We find that new histones are incorporated not only behind, but also ahead of the replication fork. We provide evidence that Rtt109, the S phase-specific acetyltransferase, stabilizes nucleosomes behind the fork, but promotes H3 replacement ahead of the fork. Unexpectedly, increased replacement ahead of the fork is independent of the primary Rtt109 acetylation target H3K56, and rather results from Rtt109 activity towards the H3 N-terminus. Our results suggest that selective incorporation of differentially modified H3s behind and ahead of the replication fork results in opposing effects on histone exchange, which may contribute to genome stability by overcoming replication-associated challenges.

genomics↗

Gene transcription as a limiting factor in protein production and cell growth

Growth rate and cell size are principle characteristics of proliferating cells, whose values depend on cellular biosynthetic processes in a way poorly understood. Protein production is critical for growth, and we therefore examined for processes limiting this production. Burdening cells with an excess of inert protein changed endogenous gene expression similarly to transcription-perturbing mutants, was epistatic to these mutants, but did not deplete respective factors from gene promoters. Mathematical modeling, corroborated by experiments, attributed this signature to a feedback which proportionally increases all endogenous gene expression, but lags at fast initiating genes already transcribed close to the maximal possible rate. As a possible benefit of maximizing transcription rates, we discuss a conflict between cell growth rate and size, which emerges above a critical cell size set by transcript abundance. We propose that biochemical limits on protein and mRNA production define the characteristic values of cell size and division time.

cell biology↗

Principles Of Cellular Resource Allocation Revealed By Condition-Dependent Proteome Profiling

Growing cells coordinate protein translation with metabolic rates. Central to this coordination is ribosome production. Ribosomes drive cell growth, but translation of ribosomal proteins competes with production of other proteins. Theory shows that cell growth is maximized when all expressed ribosomes are constantly translating. To examine whether budding yeast function at this limit of full ribosomal usage, we profiled the proteomes of cells growing in different environments. We find that cells produce an excess of ribosomal proteins, amounting to a constant {approx}8% of the proteome. Accordingly, {approx}25% of ribosomal proteins expressed in rapidly growing cells do not contribute to translation. This fraction increases as growth rate decreases. These excess ribosomal proteins are employed during nutrient upshift or when forcing unneeded expression. We suggest that steadily growing cells prepare for conditions that demand increased translation by producing excess ribosomes, at the expense of lower steady-state growth rate.

cell biology↗