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POU domain factor Brn-3b is required for the development of a large set of retinal ganglion cells

  • ,
  • Mengqing Xiang
    ,
  • Lijuan Zhou
    ,
  • Daniel S. Wagner
    ,
  • William H. Klein
    ,
  • Jeremy Nathans(corresponding author)
*Corresponding author for this work
  • University of Texas Health Science Center at Houston
    ,
  • Johns Hopkins University
    ,
  • University of Texas MD Anderson Cancer Center
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Abstract

The three members of the Brn-3 family of POU domain transcription factors are found in highly restricted sets of central nervous system neurons. Within the retina, these factors are present only within subsets of ganglion cells. We show here that in the developing mouse retina, Brn-3b protein is first observed in presumptive ganglion cell precursors as they begin to migrate from the zone of dividing neuroblasts to the future ganglion cell layer, and that targeted disruption of the Brn-3b gene leads in the homozygous state to a selective loss of 70% of retinal ganglion cells. In Brn-3b (-/-) mice other neurons within the retina and brain are minimally or not at all affected. These experiments indicate that Brn-3b plays an essential role in the development of specific ganglion cell types.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 3920-3925 (6 pages)

Journal (Volume, Issue Number)

Proceedings of the National Academy of Sciences of the United States of America (Volume 93, Issue 9)

Publication milestones

  • Published - 04/30/1996

Publication status

Published - 04/30/1996

ISSN

0027-8424

Publication IDs

  • Scopus: 0029863515
  • PubMed: 8632990

Publication metrics

Metrics

Fractional count
1
Fractional count
0.17
Fractional count
5
Fractional count
0.83
Fractional count
1
Fractional count
1
SciVal
citations
266
SciVal
FWCI
1.81
SciVal
Author count
6
SciVal
Paper percentile
98
SciVal
Top percentile
5
Scopus
citations

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Funding Details

Acknowledgment for partial support of this research is made to the National Science Foundation under Contract CTS-9710413.