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          Institute: MPI für molekulare Genetik     Collection: Department of Human Molecular Genetics     Display Documents



ID: 313140.0, MPI für molekulare Genetik / Department of Human Molecular Genetics
Characterisation of the MID1/α4
multiprotein complex
Authors:Aranda Orgillés, Beatriz
Language:English
Date of Approval (YYYY-MM-DD):2006-04
Name of University:Freie Universität
Place of University:Berlin
Audience:Experts Only
Abstract / Description:Opitz BBB/G syndrome (OS) is a congenital disorder characterised by malformations of
the ventral midline, with hypertelorism and hypospadias being the two cardinal phenotypic
manifestations. OS is genetically heterogeneous, with an autosomal and an X-linked locus.
While the gene at the autosomal locus remains to be identified, the X-chromosomal form has
been shown to be caused by mutations in the MID1 gene, which harbours mutations in
approximately 68% of patients with X-linked OS. Most of the mutations identified in OS patients
are located at the 3′ end of the MID1 open reading frame, thus affecting the C-terminus of the
The MID1 protein belongs to the RFP subfamily of the RBCC family of proteins. At its Nterminal
end it contains a RING finger, two Bboxes (Bbox1, Bbox2), and a coiled-coil domain
(RBCC domain), which are followed by a FNIII domain and a B30.2 domain (RFP domain) at its
C-terminal end. MID1 has been shown to form macromolecular cellular complexes, the
components of which were, up to now, mainly unknown. Similar to other RBCC proteins, MID1
contains several putative protein-protein interaction domains. Recently, we have shown that the
C-terminally microtubule-associated MID1 protein binds α4, a regulatory subunit of phosphatase
2A (PP2A), through the Bbox1 domain, thereby targeting the catalytic subunit of microtubuleassociated
PP2A (PP2Ac) towards ubiquitin-specific modification and degradation. MID1
mutations in the C-terminal end of the protein lead to disruption of microtubule association of
MID1 and subsequent formation of clumps in the cytosol. Despite preserving its association with
α4, C-terminally mutated MID1 can not approach the vicinity of microtubule-associated PP2Ac
and, therefore, the ubiquitination and degradation of microtubule-associated PP2Ac becomes
During this thesis, basic functions of Bbox1 and Bbox2, with respect to MID1-α4 and
MID1-microtubule interactions, were studied in detail by immunofluorescence,
immunoprecipitation and yeast two-hybrid experiments. In this way, a novel pathomechanism
for OS could be identified based on mutations in Bbox1 or Bbox2 domains of MID1 rather than
C-terminal mutations. While the Bbox1 was shown to be responsible for the interaction of MID1
with α4, the Bbox2 was demonstrated to act as a regulatory arm that couples the MID1 ubiquitin
ligase function to the microtubules by regulating the association of MID1 with both α4 and
As the main focus of this thesis, the MID1 multiprotein complex was elucidated via affinity
chromatography and mass spectrometry. Besides tubulin association, which has previously
been reported, MID1 was shown to associate with several proteins of the small ribosomal
subunit (S3, S8, p40) and other multifunctional proteins such as NPM, RACK1 and ANXA2,
which also associate with ribosomes and RNA. In addition, heat shock proteins, such as Hsp60,
Hsc70, and the multifunctional chaperones Hsp90 and p32, were identified in the complex.
Through further characterisation of the MID1 protein complex, it could be demonstrated
during this thesis that the MID1 protein, together with the mTOR target α4, forms a microtubuleassociated
mRNP that contains active polyribosomes and RNA, and thus links the translation
regulatory mTOR pathway with a microtubule-associated translation unit. This complex is likely
to participate in the transport of mRNAs to the poles of the cell, providing asymmetric mRNA
localisation and protein production. Compartmentalised protein translation is an important
prerequisite for neural crest cells to migrate and polarised cells to step into epithelialmesenchymal
transition, both essential processes during ventral midline development.
Therefore, the results of this thesis suggest a molecular basis for both the development of the
ventral midline and the pathogenesis of OS.
Moreover, it could be shown that the MID1/α4 complex integrates mRNAs of ephrinB
molecules (ligands and receptors) through G-quartet structures located in their 3´UTRs. Ephrins
and Eph receptors participate in the regulation of essential processes during the development of
the ventral midline, such as cell attachment, cell migration and embryonic patterning. Therefore,
this thesis suggests a central role for the MID1/α4 protein complex in the microtubuleassociated
compartmentalised translation of EphB receptors and ephrins-B. Interaction of the
MID1 protein complex with the mRNA of ephrin-B1 (EFNB1) is of particular interest since
mutated EFNB1 leads to the development of craniofrontonasal dysplasia, a monogenic disorder
with manifestations that are highly reminiscent of the OS phenotype. Consequently, the model
proposed here also provides an attractive explanation for the conspicuous phenotypic overlap of
the two disorders.
Document Type:PhD-Thesis
Communicated by:Hans-Hilger Ropers
Affiliations:MPI für molekulare Genetik
External Affiliations:Department of Biology, Chemistry and Pharmacy
of Freie Universität Berlin
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