DLX6 (distal-less homeobox 6)

2014-03-01   Yorick Gitton , Giovanni Levi 

Evolution des Regulations Endocriniennes, CNRS, UMR7221, Museum National dHistoire Naturelle, Paris, France

Identity

HGNC
LOCATION
7q21.3
IMAGE
Atlas Image
LEGEND
Figure 1. Genomic context of the human DLX5/DLX6 bigenic locus.
LOCUSID
ALIAS
-

Abstract

DLX6 belongs to the six-member family of DLX genes characterized by a homeobox related to that found in the insect Distal-less (Dll) gene. The six DLX genes are organized as three bigenic pairs with a tail-to-tail orientation (Zerucha et al., 2000), and located on chromosomes where HOX clusters are also found (DLX5\/DLX6; 7q21.3, syntenic to the HOXA cluster), (DLX1\/DLX2; 2q32 syntenic to the HOXD cluster) and (DLX3\/DLX4; 17q21.33 syntenic to the HOXB cluster). During embryonic development DLX genes are involved in the control of appendage and craniofacial morphogenesis and in the differentiation of reproductive organs; in the adult they play a role in bone homeostasis and in the maintenance of tissue integrity.

DNA/RNA

Atlas Image
Figure 2. The four known human DLX6 transcripts.

Description

In contrast to DLX5, no intragenic mutations have been found for DLX6. It is considered that disruption of distant regulatory elements is most usually responsible for DLX5/DLX6-related disorders in human. Breakpoint analyses of genomic deletions and chromosomal rearrangements in the congenital split-hand/split-foot malformation (SHFM type 1D, OMIM #220600), have shown that positional effect and disrupted regulatory elements controlling DLX5/DLX6 activity are involved in the pathogenesis of this developmental disorder (see further "dysmorphologies"). In-depth sequencing of the candidate regions has shown that the expression of DLX6 depends upon the activity of conserved regulatory elements shared with DLX5, and located both within the DLX5/DLX6 intergenic territory and outside of the locus (see Figure 1; Lango Allen et al., 2014). Furthermore these enhancers have been identified in all examined species - including in mouse where transgenic analyses have allowed the functional characterization of their tissue-specificity.
The status of parental imprinting of the DLX5/DLX6 locus has recently gained strong interest as these genes have been considered to be putative methylation targets of the methyl-CpG binding protein-2 (MECP2), and thus might be indirectly involved in the aetiology of the Rett syndrome, a severe X-linked neurodevelopmental disorder afflicting girls with MECP2 mutation (see further "Rett syndrome").

Transcription

Transcription from DLX6 yields four splice variants, one transcript being untranslated (see Figure 2). The three coding ones range from 666 b to 2304 b (major isoform) due to alternative splicing sites throughout the precursor transcript. Furthermore, two antisense non-coding transcripts have been characterized - one of which, Evf2 (Dlx6as/Dlx6os1; HNGC#37151), has been demonstrated to regulate transactivation from an intergenic enhancer of Dlx5/Dlx6 (Feng et al., 2006; Berghoff et al., 2013).
DLX6 sequence analysis of one sporadic SHFM patient (Ferro et al., 2001) has led to the discovery of a longer transcript endowing the N-terminus of DLX6 with an unusual dual poly-glutamine/poly-proline stretch, 11-20 CAG/CCG repeat long, which has been found to be conserved in mouse (Pfeffer et al., 2001; see further "trinucleotide repeats"). The functional consequences of these expansions upon DLX6 activity remain to be determined.

Proteins

Atlas Image
Figure 3. Structure of the three DLX6 protein isoforms. Sequence below belongs to the longest isoform. Note the N-terminal series of poly-residue stretches.

Description

DLX6 is a 175 AA helix-turn-helix homeodomain transcription factor (19.7 kDa and pI 9.9). The homeodomain spans AA 49-108 across exons 2 and 3 (see Figure 3).

Function

During mouse craniofacial morphogenesis, Dlx6 acts as transactivator of the helix-loop-helix dHand gene through a regulatory element, [ATTA/TAAT], which does not bind other Dlx factors. Noticeably, this binding is a specifically endothelin-1 signaling-dependent mechanism. Thus, despite sharing regulatory elements and subsequent expression patterns with Dlx5, the Dlx6 factor appears to be competent to exert selective roles depending upon specific cellular signalling contexts. As other DLX factors, DLX6 modulates target genes expression through a domain which is distinct from the DNA-binding homeodomain, and in association within transactivating complexes which include MSX. Composition biases in DLX6 include one poly-Gly and one-His stretches (see Figure 3).
Of note, DLX6 encodes for one long isoform endowed with a contiguous series of residue stretches including glutamine, proline, alanine and histidine (see Figure 3).
Atlas Image
Figure 4. NCBI/COBALT alignment of DLX homeoproteins. Note the disposition according to the DLX 1/4/6 versus DLX 2/3/5 clades. Indicated by a yellow box is the ultraconserved Glutamine featured by most homeoproteins at position 50 of the homeodomain.

Homology

With regards to other members of the DLX family, DLX6 belongs to the DLX1/4/6 clade based on sequence homology (see Figure 4). It shares a lack of N-terminal DLL-like domain specific to the other clade constituted by DLX2/3/5. The homeodomain remains close to all other DLX proteins.

Implicated in

Entity name
Lung cancers
Note
Neoplastic processes often result from combinatorial activity of developmental genes (Abate-Shen, 2002). Dysregulated expression of homeobox-containing genes of the distal-less family, arranged as three bigenic pairs in mammals (DLX1/2, DLX3/4 and DLX5/6; Kraus and Lufkin, 2006), has been reported to correlate with distinct oncogenic mechanisms.
DLX6 along with DLX5 is a direct MYC oncogene inducer, responsible for neoplastic initiation in many cancers, including lymphoma and lung cancers (Xu and Testa, 2009).
Entity name
Breast cancers and their bone metastases
Note
DLX6, together with DLX5, is upregulated in lung and bone metastatic cells derived from primary breast tumors in human - a pattern associated with tumour agressivity and thus, poor prognosis and increased relapses (Morini et al., 2010). Transcriptional profiling in search for prognosis markers has identified DLX6 as an upregulated candidate for high-grade astrocytomas (Phillips et al., 2006).
Entity name
Dysmorphologies
Note
DLX6 is often regarded as a functional substitute of DLX5 and autonomous regulation as been seldom observed; one rare such situation being the Endothelin-1→Endothelin-Ra→Dlx6→Hand2 signalling cascade which specifies lower jaw identity in the mouse embryo (Charité et al., 2001). As such, malformations described for DLX5 are commonly regarded as involving DLX6. In most mouse mutant models, severe phenotypes result from dual invalidation of Dlx5 and Dlx6. Malformative processes implying DLX6 will thus be simultaneously described on the DLX5 gene card.
Split hand-foot malformation (SHFM) type 1 with sensory-neural hearing loss (SHFM1D; MIM:220600). This malformative syndrome affects hands and feet alike, resulting in moderate to severe median ray deficiency with syndactily. Among the described six non-syndromic SHFM loci, one spans the DLX5/DLX6 bigenic cluster (Scherer et al., 1994; Crackower et al., 1996). Numerous reported mutations spare DLX5 or DLX6 open reading frames, suggesting it may rather be their common regulatory elements which is impacted (Robledo et al., 2002 ; Lo Iacono et al., 2008). However recently, two rare familial cases of SHFM1 have been demonstrated to result, with highest probability, from intragenic missense mutations of two critical glutamine residues in the third helix of the DLX5 homeodomain (Q178P reported in Shamseldin et al., 2012; and Q186H characterized in Wang et al., 2014). In the first case, a causal link between defective DLX5/DLX6 expression and the pathogenic mechanism impairing limb development remains to be elucidated. In the second case, the mutated DLX5 has been demonstrated to fail at transactivating its bona fide MYC target. Such an observation is not unexpected as the mutation affects Q50, the most conserved residue of all homeoproteins (see diagram), which numerous biochemical studies have demonstrated to be responsible for the specificity of the DNA recognition at the TAATT homeo-element (for review, Galliot et al., 1999).
Other pathogenetic processes: on a further note, SHFM cases have often been reported to include hearing loss, a trait consistent with a developmental role demonstrated for Dlx5/Dlx6 during ear formation in mouse embryogenesis (Acampora et al., 1999; Merlo et al., 2002; Robledo and Lufkin, 2006; Chatterjee et al., 2010; Frenz et al., 2010). Moreover, both genes are major targets of two regulator genes whose deficiencies are responsible for a related pathogenic condition, the auriculo-condylar syndrome (ACS, Rieder et al., 2012).
Anorectal malformation associated with SHFM has been reported in a family with a missense mutation in the P63 gene, a known direct upstream regulator of DLX5/DLX6 during morphogenesis (Su et al., 2013). Whether DLX5/DLX6 expression is dysregulated in this condition, and whether this trait can be functionaly associated with the phenotype, remains to be elucidated.
Entity name
Trinucleotide repeats
Note
The first DLX6 exon harbours a trinucleotide repeat region of 11 to 20 CAG triplets in normal, heterozygous subjects. This CAG repeat is highly polymorphic (Pfeffer et al., 2001). While no obvious phenotype was associated with this newly discovered polymorphism in the investigated cohort, such repeat length variations are critical determinants of colon carcinogenesis and neurodegenerative disorder when occurring in the androgen receptor and huntingtin genes, respectively.
Entity name
Rett syndrome
Note
DLX6 and DLX5 (OMIM #600028) have been controversial candidates for neurodevelopmental defects progressively afflicting young girls suffering of Rett syndrome (OMIM #312750). This late onset disorder features fatal motor abnormalities, seizures, autism and mental retardation. While the genomic sequence of the DLX5/DXL6 locus remains unaffected in all reported cases, it is a direct target of the transcriptional regulator methyl-CpG-binding protein 2 (MeCP2), which has been strongly associated to this syndrome by linkage analysis (Horike et al., 2005). While still debated (Horike et al., 2005; Schüle et al., 2007; LaSalle, 2007; Miyano et al., 2008), initial MeCP2 deficiency is considered as causing defective neurogenesis through dysregulated expression of DLX5/DLX6, due to altered chromatin state at this target locus (Horike et al., 2005; Lilja et al., 2013). Mouse mutagenesis has substantiated this hypothesis by pinpointing GABA (γ-aminobutyric acid)-releasing neurons as a major cellular target expressing Dlx5 and Dlx6, whose deficiency impairs neurogenesis in MeCP2 null mutant (Chao et al., 2010).
Entity name
Osteoporosis
Note
Mouse mutational studies have demonstrated a role for Dlx5 and Dlx6 as a major determinant of chondrogenesis and chondrocyte hypertrophy in the endochondral skeleton, throughout embryogenesis and adulthood (Samee et al., 2007; Samee et al., 2008; Samee et al., 2009). These observations pave the way for a better understanding of human osteoporosis, in particular in patients with dysfunctional regulation of bone-remodeling hormonal levels (Prall et al., 2013).
Entity name
Reproductive tract
Note
Dlx5 and Dlx6 are involved in the development and function of the reproductive tract. The dual mouse mutant for Dlx5 and Dlx6 displays abnormal urethra formation (Suzuki et al., 2008), reduced testicular steroidogenesis with feminization (Nishida et al., 2008), and early ovarian follicular depletion (Bouhali et al., 2011). A human mutation in a genomic region including DLX5 and DLX6 has been associated to a case of familial premature ovarian failure (Caburet et al., 2012).
Entity name
Teratology
Note
With regards to pharmacologically-induced teratogenesis, dysregulation of Dlx5/Dlx6 gene expression has been demonstrated to be a major step during craniofacial embryopathy induced by two compounds :
i) retinoic acid, a vitamin A derivative found in the RoAccutane ® drug, which prevents the induction of Dlx5/Dlx6 in all animal models investigated (Vieux-Rochas et al., 2007; Vieux-Rochas et al., 2010); this discovery has given strong insight into the aetiology of teratologic impact of fetal exposure to RoAccutane medication in man. Analyses of retinoic acid-induced embryopathy in mouse neurulas have demonstrated that retinoic acid exposure prevents proper induction of both Dlx5 and Dlx6 by endothelin-1 signalling. This disruption has been found to be finely tuned during a surprisingly short timeframe spanning a critical period of neurulation. This exposure creates a functional invalidation of Dlx5/Dlx6-controlled cranio-facial morphogenesis (reviewed in Gitton et al., 2010);
ii) the food contaminant ochratoxin A, a fungal toxin demonstrated to prevent Dlx5 activation in exposed mouse embryos, which later develop craniofacial malformations (Wei and Sulik, 1993; Napoletano et al., 2010). Although a causal link between Dlx5, Dlx6 and the toxin remains to be functionally demonstrated, this observation may account for teratogenesis observed in human embryos maternally exposed to the toxin (Hope and Hope, 2012; Thrasher et al., 2012).

Bibliography

Pubmed IDLast YearTitleAuthors
123602802002Deregulated homeobox gene expression in cancer: cause or consequence?Abate-Shen C et al
104339091999Craniofacial, vestibular and bone defects in mice lacking the Distal-less-related gene Dlx5.Acampora D et al
240894682013Evf2 (Dlx6as) lncRNA regulates ultraconserved enhancer methylation and the differential transcriptional control of adjacent genes.Berghoff EG et al
215050762011Allelic reduction of Dlx5 and Dlx6 results in early follicular depletion: a new mouse model of primary ovarian insufficiency.Bouhali K et al
224280462012Genome-wide linkage in a highly consanguineous pedigree reveals two novel loci on chromosome 7 for non-syndromic familial Premature Ovarian Failure.Caburet S et al
210688352010Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.Chao HT et al
117114382001Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer.Charité J et al
206371052010A symphony of inner ear developmental control genes.Chatterjee S et al
87331221996Characterization of the split hand/split foot malformation locus SHFM1 at 7q21.3-q22.1 and analysis of a candidate gene for its expression during limb development.Crackower MA et al
167050372006The Evf-2 noncoding RNA is transcribed from the Dlx-5/6 ultraconserved region and functions as a Dlx-2 transcriptional coactivator.Feng J et al
117192592001Are there CAG repeat expansion-related disorders outside the central nervous system?Ferro P et al
211083852010Retinoid signaling in inner ear development: A "Goldilocks" phenomenon.Frenz DA et al
100793621999Evolution of homeobox genes: Q50 Paired-like genes founded the Paired class.Galliot B et al
200832172010Evolving maps in craniofacial development.Gitton Y et al
222536382012A review of the diagnosis and treatment of Ochratoxin A inhalational exposure associated with human illness and kidney disease including focal segmental glomerulosclerosis.Hope JH et al
156086382005Loss of silent-chromatin looping and impaired imprinting of DLX5 in Rett syndrome.Horike S et al
166887242006Dlx homeobox gene control of mammalian limb and craniofacial development.Kraus P et al
179656112007The Odyssey of MeCP2 and parental imprinting.LaSalle JM et al
244592112014Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans.Lango Allen H et al
233489132013Novel alterations in the epigenetic signature of MeCP2-targeted promoters in lymphocytes of Rett syndrome patients.Lilja T et al
183268382008Regulation of Dlx5 and Dlx6 gene expression by p63 is involved in EEC and SHFM congenital limb defects.Lo Iacono N et al
121420282002The Dlx5 homeobox gene is essential for vestibular morphogenesis in the mouse embryo through a BMP4-mediated pathway.Merlo GR et al
185379972008DLX5 expression is monoallelic and Dlx5 is up-regulated in the Mecp2-null frontal cortex.Miyano M et al
211088122010Mutually exclusive expression of DLX2 and DLX5/6 is associated with the metastatic potential of the human breast cancer cell line MDA-MB-231.Morini M et al
200368632010Ochratoxin A induces craniofacial malformation in mice acting on Dlx5 gene expression.Napoletano M et al
182767602008Positive regulation of steroidogenic acute regulatory protein gene expression through the interaction between Dlx and GATA-4 for testicular steroidogenesis.Nishida H et al
113512652001The coding region of the human DLX6 gene contains a polymorphic CAG/CCG repeat.Pfeffer U et al
165307012006Molecular subclasses of high-grade glioma predict prognosis, delineate a pattern of disease progression, and resemble stages in neurogenesis.Phillips HS et al
240997722013Mesenchymal stem cells from osteoporotic patients feature impaired signal transduction but sustained osteoinduction in response to BMP-2 stimulation.Prall WC et al
225600912012A human homeotic transformation resulting from mutations in PLCB4 and GNAI3 causes auriculocondylar syndrome.Rieder MJ et al
169005172006Dlx5 and Dlx6 homeobox genes are required for specification of the mammalian vestibular apparatus.Robledo RF et al
194156892009Increased bone resorption and osteopenia in Dlx5 heterozygous mice.Samee N et al
177254872007Role of DLX regulatory proteins in osteogenesis and chondrogenesis.Samee N et al
79873131994Physical mapping of the split hand/split foot locus on chromosome 7 and implication in syndromic ectrodactyly.Scherer SW et al
177018952007DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.Schüle B et al
221212042012Identification of a novel DLX5 mutation in a family with autosomal recessive split hand and foot malformation.Shamseldin HE et al
237367682013Anorectal malformation associated with a mutation in the P63 gene in a family with split hand-foot malformation.Su P et al
178789162008Abnormal urethra formation in mouse models of split-hand/split-foot malformation type 1 and type 4.Suzuki K et al
222201872012A water-damaged home and health of occupants: a case study.Thrasher JD et al
210864902010Irreversible effects of retinoic acid pulse on Xenopus jaw morphogenesis: new insight into cranial neural crest specification.Vieux-Rochas M et al
244960612014Exome sequencing reveals a heterozygous DLX5 mutation in a Chinese family with autosomal-dominant split-hand/foot malformation.Wang X et al
82794841993Pathogenesis of craniofacial and body wall malformations induced by ochratoxin A in mice.Wei X et al
194978512009DLX5 (distal-less homeobox 5) promotes tumor cell proliferation by transcriptionally regulating MYC.Xu J et al
106326002000A highly conserved enhancer in the Dlx5/Dlx6 intergenic region is the site of cross-regulatory interactions between Dlx genes in the embryonic forebrain.Zerucha T et al

Other Information

Locus ID:

NCBI: 1750
MIM: 600030
HGNC: 2919
Ensembl: ENSG00000006377

Variants:

dbSNP: 1750
ClinVar: 1750
TCGA: ENSG00000006377
COSMIC: DLX6

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000006377ENST00000518156P56179
ENSG00000006377ENST00000555308G3V471

Expression (GTEx)

0
1
2
3
4
5
6
7
8
9
10

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
121936422002Specification of jaw subdivisions by Dlx genes.131
208088872010Genome-wide profiling of p63 DNA-binding sites identifies an element that regulates gene expression during limb development in the 7q21 SHFM1 locus.92
117114382001Role of Dlx6 in regulation of an endothelin-1-dependent, dHAND branchial arch enhancer.47
211088122010Mutually exclusive expression of DLX2 and DLX5/6 is associated with the metastatic potential of the human breast cancer cell line MDA-MB-231.23
177018952007DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency.21
194532612009High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men.20
206348912010Maternal genes and facial clefts in offspring: a comprehensive search for genetic associations in two population-based cleft studies from Scandinavia.18
191958022010Expression analysis and mutation detection of DLX5 and DLX6 in autism.16
244592112014Next generation sequencing of chromosomal rearrangements in patients with split-hand/split-foot malformation provides evidence for DYNC1I1 exonic enhancers of DLX5/6 expression in humans.13
291451652017Long non-coding RNA DLX6-AS1 aggravates hepatocellular carcinoma carcinogenesis by modulating miR-203a/MMP-2 pathway.13

Citation

Yorick Gitton ; Giovanni Levi

DLX6 (distal-less homeobox 6)

Atlas Genet Cytogenet Oncol Haematol. 2014-03-01

Online version: http://atlasgeneticsoncology.org/gene/52195/dlx6