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A proactive genotyp...
A proactive genotype-to-patient-phenotype map for cystathionine beta-synthase
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- Sun, Song, 1982- (författare)
- Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Comp Sci, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada;
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- Weile, Jochen (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Comp Sci, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Verby, Marta (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Wu, Yingzhou (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Comp Sci, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Wang, Yang (författare)
- Dana Farber Canc Inst, CCSB, Boston, MA 02215 USA;Harvard Med Sch, Blavatnik Inst, Dept Genet, Boston, MA 02115 USA
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- Cote, Atina G. (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Fotiadou, Iosifina (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Kitaygorodsky, Julia (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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- Vidal, Marc (författare)
- Dana Farber Canc Inst, CCSB, Boston, MA 02215 USA;Harvard Med Sch, Blavatnik Inst, Dept Genet, Boston, MA 02115 USA
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- Rine, Jasper (författare)
- Univ Calif Berkeley, Calif Inst Quantitat Biosci, Berkeley, CA 94720 USA;Univ Calif Berkeley, Dept Mol & Cell Biol, 229 Stanley Hall, Berkeley, CA 94720 USA
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- Jesina, Pavel (författare)
- Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague 12808 2, Czech Republic;Gen Univ Hosp Prague, Prague 12808 2, Czech Republic
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- Kozich, Viktor (författare)
- Charles Univ Prague, Fac Med 1, Dept Pediat & Adolescent Med, Prague 12808 2, Czech Republic;Gen Univ Hosp Prague, Prague 12808 2, Czech Republic
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- Roth, Frederick P. (författare)
- Univ Toronto, Donnelly Ctr, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Mol Genet, Toronto, ON M5S 3E1, Canada;Univ Toronto, Dept Comp Sci, Toronto, ON M5S 3E1, Canada;Mt Sinai Hosp, Lunenfeld Tanenbaum Res Inst, Toronto, ON M5G 1X5, Canada
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(creator_code:org_t)
- 2020-01-30
- 2020
- Engelska.
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Ingår i: Genome Medicine. - : BMC. - 1756-994X. ; 12:1
- Relaterad länk:
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https://doi.org/10.1...
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https://uu.diva-port... (primary) (Raw object)
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https://genomemedici...
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https://urn.kb.se/re...
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https://doi.org/10.1...
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Abstract
Ämnesord
Stäng
- Background For the majority of rare clinical missense variants, pathogenicity status cannot currently be classified. Classical homocystinuria, characterized by elevated homocysteine in plasma and urine, is caused by variants in the cystathionine beta-synthase (CBS) gene, most of which are rare. With early detection, existing therapies are highly effective. Methods Damaging CBS variants can be detected based on their failure to restore growth in yeast cells lacking the yeast ortholog CYS4. This assay has only been applied reactively, after first observing a variant in patients. Using saturation codon-mutagenesis, en masse growth selection, and sequencing, we generated a comprehensive, proactive map of CBS missense variant function. Results Our CBS variant effect map far exceeds the performance of computational predictors of disease variants. Map scores correlated strongly with both disease severity (Spearman's rho = 0.9) and human clinical response to vitamin B-6 (rho = 0.93). Conclusions We demonstrate that highly multiplexed cell-based assays can yield proactive maps of variant function and patient response to therapy, even for rare variants not previously seen in the clinic.
Ämnesord
- MEDICIN OCH HÄLSOVETENSKAP -- Medicinska och farmaceutiska grundvetenskaper -- Medicinsk genetik (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Basic Medicine -- Medical Genetics (hsv//eng)
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Sun, Song, 1982-
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Weile, Jochen
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Verby, Marta
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Wu, Yingzhou
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Wang, Yang
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Cote, Atina G.
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visa fler...
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Fotiadou, Iosifi ...
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Kitaygorodsky, J ...
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Vidal, Marc
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Rine, Jasper
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Jesina, Pavel
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Kozich, Viktor
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Roth, Frederick ...
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MEDICIN OCH HÄLS ...
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och Medicinsk geneti ...
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Genome Medicine
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Uppsala universitet