To the Editor: Blepharophimosis-ptosis-epicanthus inversus syndrome (BPES; OMIM#110100)
is featured by malformation of the eyelid, including ptosis, epicanthus inversus,
telecanthus, and reduction of the horizontal fissure length with a prevalence of 1
in 50,000.[1
2
3] If not well treated, BPES could result in strabismus and amblyopia.[4] So far,
BPES has been divided into two categories: Type I is characterized by ocular symptoms
with premature ovarian failure (POF), while POF is absent in Type II.[5]
Human forkhead box L2 (FOXL2) (OMIM#605597) belongs to the forkhead transcription
factor family.[6] The FOXL2 protein is mainly expressed in fetal and adult granulosa
cells in the ovary, functioning as an important regulator in embryonic development
of the ovaries and eyelids.[5] The FOXL2 gene consists of a single exon of 2.7 kb
located at chromosome 3q23, encoding 376 amino acids, including a 100-amino acid DNA-binding
FKH domain and a polyalanine tract. Moreover, FOXL2 has been recognized to be an important
regulator of lipid metabolism, reactive oxygen species detoxification, and carcinogenesis.[2]
To date, over 115 BPES-related mutations in over 210 BPES patients have been identified.[7]
Intragenic mutations of the FOXL2 gene take up the biggest part (71%) of the genetic
defects in BPES.[8] Frameshift mutations, nonsense mutations, and missense mutations
are all observed in the FOXL2 gene.[9] Furthermore, around 17% of indel FOXL2 mutations
are located outside its transcription unit.[1] Typically, mutations causing truncation
the protein before the polyalanine tract usually give rise to Type I, while mutations
that extend the protein usually linked with Type II.[10
11] Furthermore, our previous study has proved that FOXL2 mutation results in the
dysfunction as repressor to regulate steroidogenic acute regulatory protein (StAR)
as to contribute to the pathogenesis of BPES Type I.[1] In this study, we presented,
in detail, the clinical characteristics of a Chinese family with BPES Type II and
investigated the germline FOXL2 mutation spectrum in the affected patients.
A Chinese family with BPES Type II was ascertained through the Shanghai Xinhua Hospital
of Shanghai Jiao Tong University School of Medicine. Five individuals (I-3, I-4, II-1,
II-2, and III-1), including three affected individuals (I-4, II-2, and III-1), were
recruited [Figure 1a]. An ophthalmologist performed detailed examinations of the patients
and diagnosed BPES based on the following criteria: blepharophimosis, ptosis, epicanthus
inversus, and telecanthus [Figure 1b]. We examined DNA samples from all these patients.
In addition, the clinical data of the patients were examined in detail [Table 1].
The proband of the family (III:1), a 9-year-old boy, acquired the pathogenic gene
from his mother. All affected patients presented with typical features of BPES Type
II, including small palpebral fissure, ptosis of the eyelids, epicanthus inversus,
and telecanthus, and without POF occurrence.
Figure 1
(a) Three-generation BPES Type I pedigree. (b) Photographs of the ocular region of
the BPES families. (c) The PCR products amplified by PCR from samples from BPES patient
and unaffected family member. Gel electrophoresis of the PCR products from the BPES
patients revealed two fragments. The unaffected individuals contained a single fragment.
The left and right lane is the DNA marker (100 bp). (d) Genomic analysis of the cloned
PCR products of the FOXL2 gene, which was inserted into the multiple cloning site
(EcoRI) of the pGEM-T easy vector. This analysis reveals the FOXL2 mutation found
in affected members of this BPES Type I family. This variant was absenting in 100
control individuals, including 3 relatives of the affected families. BPES: Blepharophimosis-ptosis-epicanthus
inversus syndrome; PCR: Polymerase chain reaction.
Table 1
Clinical features of the Chinese families with BPES
Patient
Age (years)
IICD (mm)
IPFH (mm)
HPFL (mm)
Levator function (mm)
RE
LE
RE
LE
RE
LE
I-4
63
33
4
4
24
25
2
2
II-2
38
31
4
3
25
25
2
2
III-1
9
22
2
3
25
23
2
2
HPFL: Horizontal palpebral fissure length; IICD: Inner intercanthal distance; IPFH:
Vertical interpalpebral fissure height; LE: Left eye; RE: Right eye; BPES: Blepharophimosis-ptosis-epicanthus
inversus syndrome.
DNA extraction was performed as previously described. The patients’ genomic DNA was
extracted from peripheral blood leukocytes (51206; QIAGEN, Hilden, Germany). The region
of the FOXL2 gene was divided into three segments, and genomic fragments encompassing
the FOXL2 coding sequence were amplified using the following primers: FOXL2-1F: 5#-TTGAGACTTGGCCGTAAGCG-3#;
FOXL2-1R: 5#-CTCGTTGAGGCTGAGGTTGT-3# FOXL2-2F: 5#-ACAACCTCAGCCTCAACGAG-3#; FOXL2-2R:
5#-CCAGGCCATTGTACGAGTTC-3#; FOXL2-3F: 5#-GCTTCCTCAACAACTCGTGGC-3#; and FOXL2-3R: 5#-CTGCATCCTCGCATCCGTCT-3#.
Polymerase chain reaction (PCR) was performed as previously described. The PCR products
were sequenced and analyzed.
Complementary DNA (cDNA) encoding wild-type (WT) FOXL2 was prepared by PCR using primers
incorporating restriction enzyme sites. The DNA fragment amplified from the WT gene
and mutant (MT) gene was cloned into digested pseudo-cDNA (pcDNA) 3.1 and EGFP-N1
plasmids, producing pcDNA3.1-FOXL2-WT/MT and N1-FOXL2-EGFP-WT/MT.
Twenty-four hours before transfection, 293T cells were seeded into 6-cm dishes (1
× 105 cells/dish) in Dulbecco's modified Eagle's medium (DMEM; Gibco, CA, USA) containing
10% fetal calf serum (Gibco-Invitrogen, Grand Island, NY, USA) and 1% penicillin/streptomycin
and maintained at 37°C in a 5% CO2 atmosphere. The 293T cells were transfected with
N1-FOXL2-EGFP, N1-FOXL2-WT-EGFP, or N1-FOXL2-MT-EGFP using Lipofectamine 2000 reagent
(Invitrogen, Carlsbad, CA, USA). Subcellular localization/aggregation was observed
after 72 h of transfection by confocal laser scanning microscopy.
To evaluate StAR and SIRT1 gene expression, quantitative SYBR Green real-time (RT)
PCR was performed on an ABI 7300 system. Murine Leydig tumor cell line-1 (MLTC-1)
cells in six-well plates were transfected with 4 μg of pcDNA3.1 expression vector
with WT or mutant FOXL2 cDNAs and an empty pcDNA3.1 vector using Lipofectamine 2000
reagent. After 48 h, the cells were cultured in DMEM supplemented with 2% bovine serum
albumin for 2 h. Total mRNA was then extracted from the cells using TRIzol (Invitrogen,
CA, USA) according to the manufacturer's instructions. cDNA was then synthesized in
a 20 μl mixture. RT-PCR was performed with 2 μg RNA using SuperScript II (Invitrogen,
CA, USA). The housekeeping gene GAPDH was used as an endogenous control.
Patients with BPES Type II presented with two alleles: a pathogenic allele and a WT
allele [Figure 1c]. Sequencing of the coding sequence of the FOXL2 gene uncovered
a novel compound mutation (c.112_151 del, c.158_159 insCGCG) [Figure 1d]. This mutation
was not present in 100 normal subjects or in the dbSNP database (http://www.ncbi.nlm.nih.gov/SNP).
The mutated proteins, FOXL2-MT, replaced 16 amino acids (38th to 53th Aa) with RRTR,
retaining functional FKH domain and polyalanine tract [Figure 2a and 2b]. The detailed
protein sequence was listed in Supplementary Figure 1. Typically, shortened FOXL2
leads to Type I BPES. Thus, it is important to determine the mutated FOXL2 activity
as a transcript factor.
Figure 2
Computational prediction of the c.19_95 del of FOXL2 resulting in two truncated proteins.
(a) The deleted region of FOXL2 in the BPES patients is labeled in red. (b) Computational
prediction of the mutated proteins, FOXL2-MT and FOXL2-WT. BPES: Blepharophimosis-ptosis-epicanthus
inversus syndrome.
Supplementary Figure 1
The full-length sequence of FOXL2 in unaffected and BPES patients. BPES: Blepharophimosis-ptosis-epicanthus
inversus syndrome.
Click here for additional data file.
To further investigate the effect of the mutation on the subcellular localization
of the FOXL2 protein, we conducted localization studies in 293T cells. The cells were
transfected with N1-FOXL2-WT-EGFP or N1-FOXL2-MT-EGFP. Through the observation of
recombinant protein, we found that both mutant and wild-type FOXL2 are distributed
in the nucleus [Figure 3a]. The result indicated that the mutation of FOXL2 may retain
its function as a transcription factor.
Figure 3
(a) Subcellular localization of wild-type (WT) and indel mutant FOXL2 proteins. The
middle panel corresponds to the most representative subcellular localization of FOXL2
as a fusion protein with green fluorescent protein (EGFP-tagged). The left panel corresponds
to Hoechst nuclear staining. The right panel is a merged image of the previous two
images. Scale bar: 5 μM. (b and c) Relative StAR (b) and SIRT1 (c) mRNA expression
when cells were transiently transfected with the pcDNA3.1 vector, WT FOXL2 and mutant
FOXL2. StAR: Steroidogenic acute regulatory protein.
To further verify that FOXL2 regulated gene, StAR and SIRT1 expression, we performed
RT-PCR analyses to measure the endogenous mRNA expression of the StAR and SIRT1 gene
following stimulation with both the WT and mutant FOXL2 proteins. The MLTC-1 cells
transfected with the mutated FOXL2 showed the same endogenous StAR and SIRT1 expression
as wild-type group. However, the expression of mutant FOXL2 or wild-type FOXL2 was
significantly downregulated than empty vector group [Figure 3b and 3c].
FOXL2 is an evolutionarily conserved transcription factor, identified as a key regulator
of sex determination, reproductive system maturation, and eyelid development.[12]
Moreover, it has also been shown that FOXL2 also plays a key role in the pathogenesis
of polycystic ovary syndrome, keloid, and tumorigenesis. It is to note that one allele
mutation in FOXL2 could result in decreased expression and the mutation of both FOXL2
alleles could be lethal.[13] Therefore, typical BPES patients contain the heterozygous
mutation.
To date, over 110 mutations have been identified in 210 families with BPES worldwide.[1]
Before any mechanism studies were conducted, Type I BPES was hypothesized to result
from genomic truncation of FOXL2 gene.[12] Polyalanine expansion represents a common
type of in-frame mutation; these types of mutations account for 30% of the reported
mutations in the FOXL2 ORF and often give rise to Type II BPES.[1] Currently, the
new classification scheme for BPES is based on whether the FOXL2 mutation will disrupt
the protein's function as a transcription factor, causing the loss of its regulatory
control over target genes related to ovarian development, such as SIRT-1 or StAR.[11]
The major problem for Type I BPES female patients, however, is infertility rather
than eyelid malformation. For Type II patients, the major treatment is performed to
solve ocular complications as to avoid the occurrence of strabismus or amblyopia.[3]
Thus, to identify the certain type of BPES is of great significance as to provide
clinical suggestions. Here, we not only discovered that novel pattern of deletion-insertion
compound FOXL2 mutation in BPES Type II patients, but also proved the novel mutation
did not result in dysfunction of FOXL2 as a transcriptional repressor.
It is to note that POF is a multifactor-involved disease.[4] Although we have tested
typical FOXL2 (SIRT1 and StAR) regulating gene expression, we cannot eliminate other
factors that are also regulated by FOXL 2. More importantly, FOXL2 could regulate
both female reproductive system and eyelid maturation. FOXL2 mutations in Type I BPES
influence both ovarian and eyelid development; however, in Type II, it only leads
to the dysfunction in eyelid development but preserves the ability to regulate female
reproductive system development.[12]
In conclusion, we discovered a novel heterozygous deletion-insertion mutation in Chinese
families with BPES Type II. Furthermore, this is the only and first report that a
deletion-insertion compound mutation in FOXL2 gene results in BPES Type II. Our work
provides additional support for previously reported genotype-phenotype correlations
and expands the spectrum of known FOXL2 gene mutations in BPES Type II.
Supplementary information is linked to the online version of the paper on the Chinese
Medical Journal website.
Declaration of patient consent
The authors certify that they have obtained all appropriate patient consent forms.
In the form the patient(s) has/have given his/her/their consent for his/her/their
images and other clinical information to be reported in the journal. The patients
understand that their names and initials will not be published and due efforts will
be made to conceal their identity, but anonymity cannot be guaranteed.
Financial support and sponsorship
Nil.
Conflicts of interest
There are no conflicts of interest.