TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins.
TUBA1A mutations cause wide spectrum lissencephaly (smooth brain) and suggest that multiple neuronal migration pathways converge on alpha tubulins.
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DOI：
10.1093/hmg/ddq182
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发表时间：
2010-07-15
影响因子：
3.5
通讯作者：
Dobyns WB
中科院分区：
文献类型：
--
作者：
Kumar RA;Pilz DT;Babatz TD;Cushion TD;Harvey K;Topf M;Yates L;Robb S;Uyanik G;Mancini GM;Rees MI;Harvey RJ;Dobyns WB
We previously showed that mutations in LIS1 and DCX account for ∼85% of patients with the classic form of lissencephaly (LIS). Some rare forms of LIS are associated with a disproportionately small cerebellum, referred to as lissencephaly with cerebellar hypoplasia (LCH). Tubulin alpha1A (TUBA1A), encoding a critical structural subunit of microtubules, has recently been implicated in LIS. Here, we screen the largest cohort of unexplained LIS patients examined to date to determine: (i) the frequency of TUBA1A mutations in patients with lissencephaly, (ii) the spectrum of phenotypes associated with TUBA1A mutations and (iii) the functional consequences of different TUBA1A mutations on microtubule function. We identified novel and recurrent TUBA1A mutations in ∼1% of children with classic LIS and in ∼30% of children with LCH, making this the first major gene associated with the rare LCH phenotype. We also unexpectedly found a TUBA1A mutation in one child with agenesis of the corpus callosum and cerebellar hypoplasia without LIS. Thus, our data demonstrate a wider spectrum of phenotypes than previously reported and allow us to propose new recommendations for clinical testing. We also provide cellular and structural data suggesting that LIS-associated mutations of TUBA1A operate via diverse mechanisms that include disruption of binding sites for microtubule-associated proteins (MAPs).
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影响因子：
9.8
作者：
Cardoso, C;Leventer, RJ;Ledbetter, DH
通讯作者：
Ledbetter, DH
影响因子：
3.5
作者：
Morris-Rosendahl, D. J.;Najm, J.;Uyanik, G.
通讯作者：
Uyanik, G.
DOI：
10.1097/01.jnen.0000182978.56612.41
发表时间：
2005-10-01
影响因子：
3.2
作者：
Forman, MS;Squier, W;Golden, JA
通讯作者：
Golden, JA
影响因子：
19.7
作者：
BARKOVICH, AJ;JACKSON, DE;BOYER, RS
通讯作者：
BOYER, RS
影响因子：
16
作者：
Moores, CA;Perderiset, M;Milligan, RA
通讯作者：
Milligan, RA