Molecular CellSynthetic BiologyPeer-reviewed journal article
Manipulating the 3D organization of the largest synthetic yeast chromosome
Weimin ZhangiD, Luciana Lazar‐StefanitaiD, Hitoyoshi Yamashita, Michael J. SheniD, LESLIE ANN MITCHELLiD, Hikaru Kurasawa, Evgenii LobzaeviD, Viola FanfaniiD, Max A. B. HaaseiD, Xiaoji SuniD, Qingwen JiangiD, Gregory W. GoldbergiD, David M. IchikawaiD, Stephanie L. LaueriD, Laura H. McCullochiD, Nicole EasoiD, S. Jiaming Lin, Brendan R. CamellatoiD, Yinan ZhuiD, Jitong Cai, Zhuwei XuiD, Yu ZhaoiD, Maya Sacasa, Ryan Accardo, Ju Young AhniD, , Jef D. BoekeiD
Abstract
Whether synthetic genomes can power life has attracted broad interest in the synthetic biology field, especially when the synthetic genomes are extensively modified with thousands of designer features. Here we report de novo synthesis of the largest eukaryotic chromosome thus far, synIV, a 1,454,621-bp Saccharomyces cerevisiae chromosome resulting from extensive genome streamlining and modification. During the construction of synIV, we developed megachunk assembly combined with a hierarchical integration strategy, which significantly increased the accuracy and flexibility of synthetic chromosome construction and facilitated chromosome debugging. In addition to the drastic sequence changes made to synIV by rewriting it, we further manipulated the three-dimensional structure of synIV in the yeast nucleus to explore spatial gene regulation within the nuclear space. Surprisingly, we found few gene expression changes, suggesting that positioning inside the yeast nucleoplasm plays a minor role in gene regulation. Lastly, we tethered synIV to the inner nuclear membrane via its hundreds of loxPsym sites and observed transcriptional repression of the entire chromosome, demonstrating chromosome-wide transcription manipulation without changing the DNA sequences. Our manipulation of the spatial structure of the largest synthetic yeast chromosome shed light on higher-order architectural design of the synthetic genomes. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=199 SRC="FIGDIR/small/487066v2_ufig1.gif" ALT="Figure 1"> View larger version (64K): org.highwire.dtl.DTLVardef@18bf586org.highwire.dtl.DTLVardef@1a471d5org.highwire.dtl.DTLVardef@12d7690org.highwire.dtl.DTLVardef@1c32510_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIDe novo synthesis of the largest eukaryotic chromosome, synIV C_LIO_LISynIV shows similar 3D structure to wild-type IV, despite thousands of changes made to it C_LIO_LI"Inside-out" repositioning of synIV in nucleus shows minor transcriptional changes C_LIO_LIMultipoint tethering synIV to inner nuclear membrane represses transcription of whole chromosome C_LI
- organism: yeast
- assay: DNA methylation
- assay: whole-genome sequencing
- research focus: gene regulatory network inference
- research focus: variant calling
- approach: experimental assay
- Citations
- 37
- FWCI
- 3.29
- Field percentile
- top 6%
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