E-Letter responses to:
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- r-articles:
Kazunobu Sawamoto, Hynek Wichterle, Oscar Gonzalez-Perez, Jeremy A. Cholfin, Masayuki Yamada, Nathalie Spassky, Noel S. Murcia, Jose Manuel Garcia-Verdugo, Oscar Marin, John L. R. Rubenstein, Marc Tessier-Lavigne, Hideyuki Okano, and Arturo Alvarez-Buylla
- New Neurons Follow the Flow of Cerebrospinal Fluid in the Adult Brain
Science 2006; 0: 1119133v1
[Abstract]
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Published E-Letter responses:
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Synchronicity indeed
- Maurice A.M. van Steensel
(17 February 2006)
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Synchronicity indeed |
17 February 2006 |
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Maurice A.M. van Steensel, dermatologist University Hospital Maastricht
Respond to this E-Letter:
Re: Synchronicity indeed
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I read this paper with great interest, enjoying the finding that the
beating of cilia
in the brain will direct neuroblasts like a conveyor belt. I think it
might be of
interest to the readership of Science, and perhaps the authors of this
paper, to
draw attention to recent Nature Genetics papers in which the genetic basis
of
Meckel syndrome was elucidated (1, 2). This severe
developmental disorder is characterized, among other symptoms, by
exencephaly, an abnormality of the brain that results from a failure of
the rostral
neural tube to close. It turns out that at least one of the Meckel
proteins (MKS1)
is very likely a ciliary component! Together with the present report,
these
findings to me suggest that, like several other developmental processes
such as
left-right determination, neuronal migration and patterning may first and
foremost be dependent upon the beating of cilia. Processes such as neural
tube
closure may be particularly dependent. I think that the ciliary conveyor
belt is
operative throughout the neural tube -- why shouldn't it? Thus, it should
be of
interest to see whether other neural tube closure defects, such as spina
bifida,
might be caused by aberrant ciliarry beating. It should not be too
difficult to
create a mouse system where this process is disturbed in the caudal neural
tube.
References
1. M. Kyttäla et al., Nat. Genet. 38, 155-157 (2006).
2. U. M. Smith et al., Nat. Genet. 38, 191-196 (2006). |
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