Author
Listed:
- Moritz Mall
(Stanford University)
- Michael S. Kareta
(Stanford University
†Present addresses: Genetics and Genomics Group, Sanford Research, Sioux Falls, SD 57104, USA (M.S.K.); Molecular and Cellular Biology, University of California Merced, Merced, CA 95343, USA (X.G.); Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA (T.V.); Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany (P.B.); Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama 230-0045, Japan (K.R.N.).)
- Soham Chanda
(Stanford University
Stanford University)
- Henrik Ahlenius
(Lund University)
- Nicholas Perotti
(Stanford University)
- Bo Zhou
(Stanford University
Stanford University)
- Sarah D. Grieder
(Stanford University)
- Xuecai Ge
(Stanford University
†Present addresses: Genetics and Genomics Group, Sanford Research, Sioux Falls, SD 57104, USA (M.S.K.); Molecular and Cellular Biology, University of California Merced, Merced, CA 95343, USA (X.G.); Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA (T.V.); Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany (P.B.); Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama 230-0045, Japan (K.R.N.).)
- Sienna Drake
(Lund University)
- Cheen Euong Ang
(Stanford University)
- Brandon M. Walker
(Stanford University)
- Thomas Vierbuchen
(Stanford University
†Present addresses: Genetics and Genomics Group, Sanford Research, Sioux Falls, SD 57104, USA (M.S.K.); Molecular and Cellular Biology, University of California Merced, Merced, CA 95343, USA (X.G.); Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA (T.V.); Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany (P.B.); Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama 230-0045, Japan (K.R.N.).)
- Daniel R. Fuentes
(Stanford University)
- Philip Brennecke
(Stanford University
†Present addresses: Genetics and Genomics Group, Sanford Research, Sioux Falls, SD 57104, USA (M.S.K.); Molecular and Cellular Biology, University of California Merced, Merced, CA 95343, USA (X.G.); Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA (T.V.); Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany (P.B.); Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama 230-0045, Japan (K.R.N.).)
- Kazuhiro R. Nitta
(Karolinska Institutet
†Present addresses: Genetics and Genomics Group, Sanford Research, Sioux Falls, SD 57104, USA (M.S.K.); Molecular and Cellular Biology, University of California Merced, Merced, CA 95343, USA (X.G.); Department of Neurobiology, Harvard Medical School, Boston, Massachusetts 02115, USA (T.V.); Leibniz-Institute for Molecular Pharmacology, 13125 Berlin, Germany (P.B.); Division of Genomic Technologies, RIKEN Center for Life Science Technologies, Yokohama 230-0045, Japan (K.R.N.).)
- Arttu Jolma
(Karolinska Institutet)
- Lars M. Steinmetz
(Stanford University
Genome Biology Unit, European Molecular Biology Laboratory (EMBL))
- Jussi Taipale
(Karolinska Institutet
Genome Scale Biology Program, University of Helsinki)
- Thomas C. Südhof
(Stanford University)
- Marius Wernig
(Stanford University)
Abstract
The neuron-specific transcription factor Myt1l represses many somatic lineage programs, but not the neuronal lineage program, to both induce and maintain neuronal identity.
Suggested Citation
Moritz Mall & Michael S. Kareta & Soham Chanda & Henrik Ahlenius & Nicholas Perotti & Bo Zhou & Sarah D. Grieder & Xuecai Ge & Sienna Drake & Cheen Euong Ang & Brandon M. Walker & Thomas Vierbuchen & , 2017.
"Myt1l safeguards neuronal identity by actively repressing many non-neuronal fates,"
Nature, Nature, vol. 544(7649), pages 245-249, April.
Handle:
RePEc:nat:nature:v:544:y:2017:i:7649:d:10.1038_nature21722
DOI: 10.1038/nature21722
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Cited by:
- Gintautas Vainorius & Maria Novatchkova & Georg Michlits & Juliane Christina Baar & Cecilia Raupach & Joonsun Lee & Ramesh Yelagandula & Marius Wernig & Ulrich Elling, 2023.
"Ascl1 and Ngn2 convert mouse embryonic stem cells to neurons via functionally distinct paths,"
Nature Communications, Nature, vol. 14(1), pages 1-14, December.
- Ravneet Jaura & Ssu-Yu Yeh & Kaitlin N. Montanera & Alyssa Ialongo & Zobia Anwar & Yiming Lu & Kavindu Puwakdandawa & Ho Sung Rhee, 2022.
"Extended intergenic DNA contributes to neuron-specific expression of neighboring genes in the mammalian nervous system,"
Nature Communications, Nature, vol. 13(1), pages 1-18, December.
- Luke F. Nunnelly & Melissa Campbell & Dylan I. Lee & Patrick Dummer & Guoqiang Gu & Vilas Menon & Edmund Au, 2022.
"St18 specifies globus pallidus projection neuron identity in MGE lineage,"
Nature Communications, Nature, vol. 13(1), pages 1-16, December.
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