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Sierra Heras, L.

Publications and source records attributed to Sierra Heras, L..

3 recordsLinked to original sources

Assembly and cell-free expression of a partial genome for the synthetic cell

The de novo design and assembly of a DNA genome represents an important milestone toward the construction of a minimal synthetic cell. The genome must contain all the instructions to enable primary cellular functions, probably comprising over 150 genes with a total size over 200 kb. Here, we designed and built a partial synthetic genome that satisfies the requirements for its expression in PURE system--a minimal transcription-translation machinery reconstituted from purified elements--and its replication by the protein-primed {varphi}29 DNA replication system. The partial minimal synthetic genome (MSG) has a size of 41 kb, was assembled in yeast from 14 fragments, and harbors genes for phospholipid biosynthesis, DNA replication, and cell division. Yeast marker fragments were added between coding fragments to facilitate screening of correct assemblies and a BAC backbone was included to enable transfer from yeast to E. coli for amplification. Synthesis of all MSG-encoded proteins in PURE system was confirmed by liquid chromatography-mass spectrometry and fluorescence measurements. Moreover, we demonstrate successful compartmentalization and expression of the MSG in liposomes, as well as full-length replication of the linearized MSG by the {varphi}29 DNA replication machinery. This work provides proof-of-concept for the bottom-up assembly and cell-free expression of a functional genome for a minimal synthetic cell.

synthetic biology↗

Autocatalytic selection of gene functions in vitro

The integration of biological functions into a single operating system is considered a major challenge in the construction of a synthetic cell1-3. We present autocatalytic selection (ACS) of gene functions as a driver for integrating biological modules in vitro. A gene of interest (GOI) is introduced into a minimal DNA self-replicator based on the {phi}29 replication machinery4 and the function of the GOI is linked to transcription, translation or DNA replication through a positive feedback loop. As the encoded function eventually promotes DNA self-replication, the gene variants with greater activity are selected. Using different coupling mechanisms, we demonstrate ACS of three functions: transcription, synthesis of a deoxynucleoside triphosphate for DNA replication, and {beta}-galactosidase activity. The latter example illustrates how a function that is unrelated to the Central Dogma can be selected. This work paves the way for ACS-driven Darwinian evolution of virtually any biomolecule in vitro, streamlining the construction of increasingly complex synthetic cells as well as the engineering of biotechnologically relevant enzymes.

synthetic biology↗

A synthetic cell with integrated DNA self-replication and membrane biosynthesis

The emergence, organization, and persistence of cellular life are the result of the functional integration of metabolic and genetic networks. Here, we engineer phospholipid vesicles that can operate three essential functions, namely transcription-translation of a partial genome, self-replication of this DNA program, and membrane synthesis. The synthetic genome encodes six proteins and its compartmentalized expression produces active liposomes with distinct phenotypes demonstrating successful module integration. Our results reveal that genetic factors exert a stronger control over DNA replication and membrane synthesis than metabolic crosstalk or module co-activity. By showing how genetically encoded functions derived from different species can be integrated in liposome compartments, our work opens new avenues for the construction of autonomous and evolving synthetic cells.

synthetic biology↗