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Accepted manuscripts are peer-reviewed but have not been through the copyediting, formatting, or proofreading process. Copyright © 2016 the authors This Accepted Manuscript has not been copyedited and formatted. The final version may differ from this version. Research Articles: Development/Plasticity/Repair Lhx2 interacts with the NuRD complex and regulates cortical neuron subtype determinants Fezf2 and Sox11 Bhavana Muralidharan 1 , Zeba Khatri 1 , Upasana Maheshwari 1 , Ritika Gupta 1 , Basabdatta Roy 1 , Saurabh J. Pradhan 2 , Krishanpal Karmodiya 2 , Hari Padmanabhan 1,3,4 , Ashwin Shetty 1,3 , Chinthapalli Balaji 1 , Ullas Kolthur- Seetharam 1 , Jeffrey D. Macklis 3,4 , Sanjeev Galande 2 and Shubha Tole 1 1 Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai-400005, India 2 Indian Institute of Science, Education, and Research, Pune- 411008, India. 3 Department of Stem Cell and Regenerative Biology 4 Center for Brain Science, and Harvard Stem Cell Institute, Harvard University, Cambridge, MA-02138 USA. DOI: 10.1523/JNEUROSCI.2836-16.2016 Received: 5 September 2016 Revised: 26 October 2016 Accepted: 7 November 2016 Published: 1 December 2016 Author contributions: B.M., Z.K., U.M., S.J.P., H.P., A.S.S., U.K.-S., S.G., and S.T. designed research; B.M., Z.K., U.M., R.G., B.R., S.J.P., H.P., A.S.S., and C.B. performed research; B.M., Z.K., U.M., R.G., B.R., K.K., H.P., A.S.S., U.K.-S., J.D.M., S.G., and S.T. analyzed data; B.M., Z.K., H.P., A.S.S., J.D.M., and S.T. wrote the paper. Conflict of Interest: The authors declare no competing financial interests We thank Y. Li and E. Monuki for kind gifts of mouse lines used in this study; T. Saito, T. Ohshima, L. Carlsson, E. Monuki, S. McConnell, A. Stoykova, C. Ragsdale and R. Hevner for gifts of plasmid DNA. We thank P. Arlotta, D. Jabaudon, S. Lodato and members of the Tole lab for helpful discussion, D. Jabaudon for critical comments on the manuscript, Dr. S. Suryavanshi and the TIFR Animal Facility for excellent support, and L. D'souza for technical assistance. This work was supported by a Wellcome Trust-Department of Biotechnology India Alliance Early Career Fellowship (BM), and intramural funds from TIFR-DAE (ST). Corresponding author: [email protected] Cite as: J. Neurosci 2016; 10.1523/JNEUROSCI.2836-16.2016 Alerts: Sign up at www.jneurosci.org/cgi/alerts to receive customized email alerts when the fully formatted version of this article is published.

Lhx2 interacts with the NuRD complex and regulates ... · 12/1/2016  · Seetharam 1, Jeffrey D. Macklis 3,4, Sanjeev Galande 2 and Shubha Tole 1 1 Department of Biological Sciences,

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Page 1: Lhx2 interacts with the NuRD complex and regulates ... · 12/1/2016  · Seetharam 1, Jeffrey D. Macklis 3,4, Sanjeev Galande 2 and Shubha Tole 1 1 Department of Biological Sciences,

Accepted manuscripts are peer-reviewed but have not been through the copyediting, formatting, or proofreadingprocess.

Copyright © 2016 the authors

This Accepted Manuscript has not been copyedited and formatted. The final version may differ from this version.

Research Articles: Development/Plasticity/Repair

Lhx2 interacts with the NuRD complex and regulates cortical neuron subtypedeterminants Fezf2 and Sox11

Bhavana Muralidharan1, Zeba Khatri1, Upasana Maheshwari1, Ritika Gupta1, Basabdatta Roy1, Saurabh J.

Pradhan2, Krishanpal Karmodiya2, Hari Padmanabhan1,3,4, Ashwin Shetty1,3, Chinthapalli Balaji1, Ullas Kolthur-

Seetharam1, Jeffrey D. Macklis3,4, Sanjeev Galande2 and Shubha Tole1

1Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai-400005, India2Indian Institute of Science, Education, and Research, Pune- 411008, India.3Department of Stem Cell and Regenerative Biology4Center for Brain Science, and Harvard Stem Cell Institute, Harvard University, Cambridge, MA-02138 USA.

DOI: 10.1523/JNEUROSCI.2836-16.2016

Received: 5 September 2016

Revised: 26 October 2016

Accepted: 7 November 2016

Published: 1 December 2016

Author contributions: B.M., Z.K., U.M., S.J.P., H.P., A.S.S., U.K.-S., S.G., and S.T. designed research; B.M.,Z.K., U.M., R.G., B.R., S.J.P., H.P., A.S.S., and C.B. performed research; B.M., Z.K., U.M., R.G., B.R., K.K.,H.P., A.S.S., U.K.-S., J.D.M., S.G., and S.T. analyzed data; B.M., Z.K., H.P., A.S.S., J.D.M., and S.T. wrote thepaper.

Conflict of Interest: The authors declare no competing financial interests

We thank Y. Li and E. Monuki for kind gifts of mouse lines used in this study; T. Saito, T. Ohshima, L. Carlsson,E. Monuki, S. McConnell, A. Stoykova, C. Ragsdale and R. Hevner for gifts of plasmid DNA. We thank P.Arlotta, D. Jabaudon, S. Lodato and members of the Tole lab for helpful discussion, D. Jabaudon for criticalcomments on the manuscript, Dr. S. Suryavanshi and the TIFR Animal Facility for excellent support, and L.D'souza for technical assistance. This work was supported by a Wellcome Trust-Department of BiotechnologyIndia Alliance Early Career Fellowship (BM), and intramural funds from TIFR-DAE (ST).

Corresponding author: [email protected]

Cite as: J. Neurosci 2016; 10.1523/JNEUROSCI.2836-16.2016

Alerts: Sign up at www.jneurosci.org/cgi/alerts to receive customized email alerts when the fully formattedversion of this article is published.

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Fezf2 Sox11

1Department of Biological Sciences, Tata Institute of Fundamental Research, Mumbai-

400005, India; 2Indian Institute of Science, Education, and Research, Pune- ,

India. 3Department of Stem Cell and Regenerative Biology, and 4Center for Brain

Science, and Harvard Stem Cell Institute, Harvard University, Cambridge, MA-

USA.

* Corresponding author: [email protected]

Current affiliation: Department of Stem Cell and Regenerative Biology, and 4Center for

Brain Science, and Harvard Stem Cell Institute, Harvard University, Cambridge, MA-

02138 USA

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Fezf2 Sox11

Fezf2 Sox11

Fezf2

Ctip2

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Fezf2 Sox11

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Fezf2

in vivo

Fezf2

Fezf2

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Fezf2 Sox11 that

Lhx2

Lhx2

Lhx2

Fezf2

Fezf2 Sox11

Fezf2 Sox11

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Fezf2 Sox11

Fezf2

Fezf2

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et al

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β

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In situ

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Lhx2

Lhx2

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Lhx2

Lhx2

Lhx2

Lhx2

Tbr1

Lhx2

ER81 Id2, Fezf2

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Fezf2 Sox11

Fezf2 Sox11

Fezf2 Sox11

Lhx2

Fezf2

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Lhx2cKO Sox11,

Lhx2cKO

Fezf2

Fezf2/Sox11

Fezf2 Sox11

Lhx2

Fezf2

Sox11

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Fezf2 Sox11

Fezf2 Sox11

Fezf2

Sox11

Fezf2 Sox11

Lhx2cKO

Fezf2 Sox11

Lhx2cKO

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Fezf2 Sox11

Fezf2

Lhx2

Lhx2-GFP in utero

Lhx2

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Fezf2

Fezf2

Fezf2 Sox11

Fezf2 Sox11

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Fezf2

Lhx2

Lhx2 Lhx2

Lhx2 Fezf2

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Lhx2

Lhx2

Lhx2

Lhx2

Lhx2

Fezf2 COUP-TF1, CB1R and Cux2

Fezf2

Fezf2

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Fezf2

Ctip2

Ctip2

Fezf2 Fezf2

Fezf2

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Fezf2

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Lhx2

Lhx2cKO

Tbr1 Fezf2,

ER81, and Id2

Fezf2 Sox11

Fezf2 Sox11

Fezf2 Sox11

Fezf2 Sox11

Fezf2 Sox11

Fezf2 Sox11

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Fezf2 Sox11

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The image of the silver stained gel shown in (A) has been cropped to remove the lanes

corresponding “unbound” fractions of control IgG and Lhx2 IP that were on the left of the

marker lane. The Western blots shown in (B) and (C) are cropped from full length

Western blots. The original uncropped images are available upon request.

Fezf2 Sox11

Lhx2cKO

Fezf2 Sox11

GFP Lhx2-GFP

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Lhx2-GFP

Lhx2

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