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BMC Genomics

Open Access

De novo mutations in ARID1B associated with both syndromic and non-syndromic short stature

  • Yongguo Yu1, 3,
  • RuEn Yao2,
  • Lili Wang1,
  • Yanjie Fan1,
  • Xiaodong Huang3,
  • Joel Hirschhorn4, 5, 6,
  • Andrew Dauber7 and
  • Yiping Shen2, 8, 9, 10Email author
BMC Genomics201516:701

https://doi.org/10.1186/s12864-015-1898-1

Received: 3 June 2015

Accepted: 8 September 2015

Published: 16 September 2015

Abstract

Background

Human height is a complex trait with a strong genetic basis. Recently, a significant association between rare copy number variations (CNVs) and short stature has been identified, and candidate genes in these rare CNVs are being explored. This study aims to evaluate the association between mutations in ARID1B gene and short stature, both the syndromic and non-syndromic form.

Results

Based on a case-control study of whole genome chromosome microarray analysis (CMA), three overlapping CNVs were identified in patients with developmental disorders who exhibited short stature. ARID1B, a causal gene for Coffin Siris syndrome, is the only gene encompassed by all three CNVs. A following retrospective genotype-phenotype analysis based on a literature review confirmed that short stature is a frequent feature in those Coffin-Siris syndrome patients with ARID1B mutations. Mutation screening of ARID1B coding regions was further conducted in a cohort of 48 non-syndromic short stature patients,andfour novel missense variants including two de novo mutations were found.

Conclusion

These results suggest that haploinsufficient mutations of ARID1B are associated with syndromic short stature including Coffin-Siris syndrome and intellectual disability, while rare missense variants in ARID1B are associated with non-syndromic short stature. This study supports the notion that mutations in genes related to syndromic short stature may exert milder effect and contribute to short stature in the general population.

Keywords

ARID1B Short statureHaploinsufficiencyCoffin-Siris SyndromeChromatin remodeling

Background

Human height is a quantitative trait that follows a Gaussian distribution. Short stature is typically defined as a height more than 2 standard deviations (SD) below the corresponding mean height for a given age, gender and ethnic population. Individuals with short stature include those at the tail of the normal distribution (not necessary associated with any disorders) as well as individuals with rare disorders that restrict growth. Genome-wide association studies (GWAS) have identified over 400 independent loci associated with height in the general population which collectively explain ~20 % of the variation in adult height [1]. Rare variants with larger effects have been found in a number of genes leading to syndromic short stature disorders. For example, the SHOX gene was identified as the gene responsible for short stature in Turner syndrome [2] and Leri-Weill syndrome [3]. Recently, we demonstrated a significant association between low-frequent copy number deletions and short stature, supporting the hypothesis that rare haploinsufficient genes play significant roles in human growth [4]. We further demonstrated that an increased burden of rare deletions may also contribute to short stature in a non-clinically ascertained population, underscoring the concept that milder defects in genes known to cause syndromic short stature may contribute to short stature in the general population.

In this study, we focus on a recurrent CNV detected in patients with short stature. We propose that the ARID1B gene, which is the only gene intercepted by three CNVs, is a novel short stature gene. We provide additional evidence supporting that ARID1B mutations are associated with both syndromic and non-syndromic short stature.

Methods

CNV detection and evaluation

Whole genome microarray (Agilent 244K) was performed to detect structural variants in a clinical cohort. Subjects were eligible if they had a height measurement recorded between the ages of 2 and 20 years and had a chromosomal microarray performed as part of their clinical evaluation. All information was obtained with appropriate consent from Boston Children’s hospital [M09-06-0290]. Subjects with aneuploidy and poor microarray quality were not included, leaving a final sample size of 4,411 individuals including 415 patients with short stature, 196 patients with tall stature and 3800 patients with normal stature. All CNV data were called with NEXUS software (BioDiscovery, El Segundo, California). The recurrent copy-number variations involving ARID1B gene were validated by multiplex ligation-dependent probe amplification (MLPA). MLPA probe and reagents from MRC Holland (SALSA MLPA P433 ARID1A-ARID1B probemix). Data analysis and visualization was done on Coffalyzer software. A CNV is defined as non-benign when it does not overlap with CNV reported in DGV (Database of Genomic variants) or overlaps with CNV with less than 1 % population frequency in DGV. Non-benign recurrent or overlapping CNVs were identified in the subjects with short stature and compared to their occurrence in normal stature population. The UCSC genome browser’s custom track was used to depict the overlapping nature of CNVs and to delineate the minimal region of overlap (MRO).

Literature review of height of patients with ARID1B deletion or mutation

We identified a total of 70 individuals carrying ARID1B deletions or mutations from a Pubmed search and the DECIPHER database. 65 of them had information on height. We converted all height parameters available to Z-scores based on CDC growth charts (http://www.cdc.gov/growthcharts/zscore.htm).

Mutation screening in 48 non-syndromic short stature Chinese patients

Forty-eight non-syndromic short stature Chinese patients were recruited in Shanghai Children’s Medical Center. Their age, gender and height information are included in Additional file 1. The inclusion criteria were individuals with height below 3rd percentile without a clinical diagnosis of intellectual disability or developmental delay. All information was obtained with appropriate consent based on requirements of Shanghai Children’s Medical Center【SCMC-IRB-K2013007】.Subjects were randomly selected in non-syndromic short stature patients. Since it is unclear yet if ARID1B affects hormone-related pathways, we did not use hormonal status as a criteria for subject selection. Genomic DNA was extracted from peripheral blood of all participants using QIAamp Blood DNA Mini kit®. Mutation screening for all coding regions of ARID1B were done by Polymerase chain reaction (PCR) amplification followed by Sanger sequencing. Sequence variants were evaluated with mutation surveyor (Soft Genetics, State College, PA) and their potential functional impact was predicted using insilico prediction programs including SIFT [5], Polyphen2 [6], Condel [7] and Align-GVGD [8]. Paternity tests were performed with short tandem repeat (STR) markers for the two probands with de novo variants (using AmpFLSTR® Identifiler® PCR amplification kit). The study was reviewed and approved by the SCMC ethical committee and all participants or their parents signed an informed consent form. In addition, we compared the variant frequency in the ARID1B coding regions detected by exome sequencing to that of 494 normal Chinese controls. The normal Chinese controls were age and gender matching Chinese individuals of normal height, weight and were recruited from multiple geographic areas for an effort to create a common sequence variants database of normal Chinese children.

Results

Copy number imbalances involving ARID1Bin patients with short stature and developmental disorder

Four thousand four hundred eleven individuals in the clinical population met our inclusion criteria (as described in methods), including 415 patients with short stature, 196 patients with tall stature and 3800 patients with normal stature. Three individuals with copy number variants encompassing ARID1B were identified among 415 patients with short stature who underwent clinical microarray analysis at Boston Children’s Hospital. The locations of the two deletions and one duplication in relation to the ARID1B gene are shown in Fig. 1.
Fig. 1

Three individuals with copy number variants encompassing ARID1B shown as tracks in the UCSC genome browser

Figure 1

Red tracks indicate deletion and blue track indicates duplication. The numbers associated with each track are the Z-scores of patient’s height.

The first patient (patient A) carries a 658 kb de novo deletion at 6q25.3 which affected only ARID1B; the second patient (patient B) carries a 6.8 Mb de novo deletion at 6q25.1-q25.3 which overlaps with the deletion in Patient 1. The height Z-score for both patients are -2.3 and -2.1 respectively. The patient with the duplication (patient C) was a 13-year-old Caucasian girl who carries a 207 Kb maternally inherited intragenic duplication at 6q25.3. Her height Z-score was -2.7. The mother’s height is below average (Z = -0.33) but not short. In addition to short stature, all three patients exhibited language impairment, facial malformation and intellectual disability. Thus all three patients exhibited syndromic short stature. Detailed clinical phenotypes and their growth curves can be found in Additional files 1 & 2.

There were no CNVs involving ARID1B in 3800 patients with normal stature and 196 patients with tall stature in our clinical population.

Short stature is a frequent feature associated with patients with ARID1B mutations

A total of 70 patients with mutations in ARID1B (including translocation, deletion, duplication, nonsense and truncating mutations) have been described in the literature and Decipher database, many of whom have Coffin-Siris syndrome. We summarize the available clinical features of these patients in Table 1. Five patients had no height information. 22 out of the remaining 65 patients (33.8 %) had short stature. 90 % of patients have height Z-scores below -1 SD. None of the patients had height Z-scores above 0 SD. The average available Z score among patients with mutations in ARID1B is -1.86 SD. Thus, growth retardation and short stature is a common feature associated with mutations in ARID1B and Coffin-Siris syndrome.
Table 1

Clinical features of patients with ARID1B mutations

Cases from literature review

Case IDa

1

2

3

4

5

6

7

8

9

10

11

12

13

14

15

16

17

18~45

46

47

48

49

50

51

52

Gender

M

F

M

F

F

F

F

F

F

F

M

M

F

F

F

M

M

NS

F

M

F

M

M

F

F

Genomic defectb

Trans

Del

Del

Del

Del

Del

Del

Del

Del

Dup

Nonsense

Fx

Nonsense

Fx

Fx

Nonsense

Fx

 

Del

Del

Del

Del

Del

Del

Del

Height (age)

117 cm (7.5 y)

84 cm (2 y 11 m)

1.59 cm (46 y)

44.5 cm (at birth)

66.8 cm (9 M)

152 cm (18 y)

124 cm (8 y 9 m)

112 cm (9.5 y)

10th (3 y 3 m)

3–10th (4 y 11 m)

3-10th (3 y 5 m)

<3rd (7 y 3 m)

<3rd (12 y 8 m)

10–25th (4 y)

25–50th (6 y 3 m)

50th (17 y)

<3rd (20 y)

11 % (3/27) <−2.5SD

NS

NS

NS

52 cm (50th )

89.2 cm (2 y 9 m)

48 cm (at birth)

64 cm (10 m)

Z-score

−1.8

−2.5

−3.5

<−2.0

−2

−1.65

−2

−4

−1.2

−1.5

−1.5

−2

−2

−1.2

−0.6

0

−2

 

−1.5

−3.5

−2.6

0

−1.34

−1.65

−2.7

OFC (age)

+1.4 SD

−0.7 SD

−0.75 SD

NA

Z=0

25–50th

Z=0

−2.5 SD

10–25th

<3rd

50th

25–50th

25–50th

75th

75th

>97th

<3rd

0 % (0/27) <−2.5SD

NS

Z=−0.75

NS

75th

46.2 cm

31 cm

Z=−4.3

DD/ID

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

89 % (25/28)

+

+

+

+

+

+

+

ACC

+

NA

NA

 

NA

Partial

Partial

+

+

+

NA

  

NA

+

NA

 

36 % (9/25)

NS

NS

+

NS

NS

 

+

Hypotonia

+

+

NS

+

+

+

+

+

+

+

+

+

+

+

+

  

85 % (23/27)

NS

NS

NS

+

NS

+

NS

Seizure

  

NS

  

+

+

+

    

+

 

+

+

 

20 % (5/20)

NS

NS

NS

NS

NS

+

NS

ASD

+

+

+

+

NS

+

    

+

      

NS

NS

NS

NS

NS

NS

NS

NS

Language impairment

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

+

100 % (28/28)

+

+

+

+

NS

+

+

Malformation

Coarse facial

NS

NS

+

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

+

+

 

NS

+

+

+

Low hair line

+

NS

NS

+

NS

+

+

+

NS

NS

NS

NS

NS

NS

NS

NS

NS

64 % (18/28)

  

+

NS

NS

NS

NS

Hypertrichosis

 

+

NS

NS

NS

NS

+

+

     

+

+

  

93 % (26/28)

   

NS

NS

NS

NS

Ear

+

NS

+

NS

NS

NS

NS

+

+

+

+

+

+

+

+

+

+

50 % (14/28)

NS

NS

NS

+

+

+

+

Eye

+

NS

+

+

+

+

+

+

+

+

+

+

+

+

NS

+

NS

65 % (17/26)

+

+

+

+

+

+

+

Nose

+

NS

+

+

NS

+

NS

+

+

+

NS

+

+

+

+

NS

NS

52 % (14/27)

NS

NS

NS

+

+

+

+

Mouth/lips/palate

+

+

+

 

+

+

+

+

NS

+

+

+

+

+

+

NS

+

78 % (21/27)

NS

NS

NS

+

+

+

+

Skeletal

NS

+

+

NS

NS

+

NS

+

NS

+

NS

NS

NS

NS

NS

NS

+

17 % (2/12)

NS

NS

NS

NS

NS

NS

NS

Limb/extremeties

+

+

+

+

+

+

+

+

NS

+

+

+

+

+

NS

NS

+

>75 %

+

NS

NS

+

NS

NS

+

 

Cases from literature review

 

Cases from decipher database

Our cases from microarray and sequence

Case ID

53

54

55

56

57

58

59

60

61

62

63

64

 

65

66

67

68

69

70

A

B

C

D

E

F

G

Gender

M

F

M

M

M

M

M

M

M

F

0

0

 

M

F

F

NS

NS

M

M

M

F

M

M

F

F

Genomic defect

Del

Del

Del

Del

Del

Del

Del

Fx

Nonsense

Nonsense

Fx

Del

 

Del

Del

Del

Del

Del

Dup

Del

Del

Dup

Missense

Missense

Missense

Missense

Height (age)

69.5 cm (10 m)

66 cm (9 m)

63.5 cm (7 m)

162 cm (16 y 6 m)

47 cm (14 days)

55.5 cm (at birth)

46.6 cm (3 m)

 

2/5 has short stature

 

Short stature

NS

NS

NS

NS

NS

<3rd

3rd

−3 SD (12 y 8 m)

−3 SD (3 y 6 m)

−3 SD (3 y 2 m)

−2 SD (9 y 8 m)

−2 SD (8 y 9 m)

Z-score

−1.56

−2.0

−2.0

−1.7

<−1.65

−1.65

<−3.0

 

−2

NS

NS

NS

NS

NS

−2.3

−2.1

−2.7

−2

−2

−2

−2

OFC (age)

Z=−4.5

Z=0

Z<−2.0

53 cm

Z<−1.65

Z=1.65

Z<−3.0

NS

NS

NS

NS

NS

 

NA

  

NS

NS

NA

50th

2nd

98th

NS

NS

NS

NS

DD/ID

+

+

+

+

+

+

+

+

+

+

+

+

 

+

+

+

+

+

+

+

+

+

    

ACC

+

+

NS

NS

+

NS

+

NS

NS

NS

NS

NS

 

NA

+

NS

NS

NS

NS

+

+

 

NS

NS

NS

NS

Hypotonia

+

+

NS

NS

NS

+

+

4/5 have hypotonia

 

NA

+

NS

NS

NS

NS

+

+

+

    

Seizure

NS

NS

NS

+

NS

NS

NS

2/5 have seizure

 

NA

NS

NS

NS

NS

+

+

      

ASD

NS

NS

NS

+

NA

NA

NA

NS

NS

NS

NS

NS

 

+

NS

NS

NS

+

NS

 

+

     

Language impairment

NS

NS

NS

+

NS

NS

NS

NS

NS

NS

NS

NS

 

+

NS

NS

NS

+

NS

+

+

+

    

Malformation

Coarse facial

+

+

NS

NS

NS

+

 

+

+

+

+

+

 

+

NS

NS

NS

+

NS

+

+

     

Low hair line

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

NS

 

+

NS

NS

NS

NS

NS

 

+

+

    

Hypertrichosis

NS

NS

NS

NS

+

NS

NS

+

+

+

+

+

 

NS

NS

NS

NS

+

NS

 

+

     

Ear

+

+

NS

+

+

+

+

4/5 have abnormal ears

 

NS

NS

+

+

NS

NS

+

+

NS

    

Eye

+

+

+

+

+

+

+

1/5 with vision problem

 

+

NS

+

+

NS

NS

+

+

+

    

Nose

+

NS

+

+

+

+

+

+

+

+

+

+

 

+

NS

NS

NS

NS

NS

+

+

NS

    

Mouth/lips/palate

+

+

+

+

NS

NS

+

+

+

+

+

+

 

+

NS

NS

NS

NS

+

+

+

+

    

Skeletal

NS

NS

NS

NS

NS

NS

NS

3/4 have spinal anomalies

 

NS

NS

NS

NS

NS

+

+

+

+

    

Limb/extremeties

NS

+

+

+

+

NS

+

+

+

+

+

+

 

+

NS

NS

+

NS

NS

+

+

+

    

a1–8 Halgren et al., 9–17 Hoyer et al., 18–45 Santen et al. (2013), 46-48 santen et al. (2012), 49 Michelson et al., 50–53 Nagamani et al., 54 Pirola et al., 55 Narahara et al., 56–57 Sukumar et al., 58 Hopkin et al., 59 Meng et al., 60–64 Tsurusaki et al., 65–70 from decipher database

bThe following abbreviations are used: F female, M male, OFC occipital-frontal circumference, + present, absent, NA not analyzed, NS not stated, ACC agenesis of corpus callosum, ASD atrial septum defect, trans translocation, del deletion, dup duplication, fx frameshift

ARID1B mutations in non-syndromic patients with short stature

We sequenced the coding regions and intron-exon boundaries of ARID1B in 48 non-syndromic short stature Chinese patients. We detected four missense variants (Fig. 2). Variants c.2351C > T and c.4727C > T in patients D and E respectively were inherited from their fathers and the c.2351 variant was present in a sister of normal height as well. Variants c.4346G > C and c.5998G > T in patients F and G were not identified in either parent. Paternity test confirmed the biological relationship between the probands and their parents (data available in Additional file 3), thus these two missense variants are de novo changes in the probands. Provocative growth hormone (GH) testing with intravenous infusion of Arginine and oral administration of clonidine was performed in the patients, following routine procedures. Patient E, F and G exhibited partial growth hormone deficiency by provocative GH testing (5-7ng/ml).Patient D had a normal growth hormone level (15.272ng/ml). None of them had intellectual disability or language impairment. Thus they are all considered to have non-syndromic short stature. Detailed clinical information of the four patients is presented in Additional file 1.
Fig. 2

ARID1B Sanger sequencing data of four patients and their parents

The four missense variants were all predicted to be deleterious by SIFT, PolyPhen2 and Condel (Additional file 4). They were novel variants and absent from 494 Chinese controls, the NHLBI Exome Variant Server 6500 dataset (http://evs.gs.washington.edu/EVS/) and the ExAC database (http://exac.broadinstitute.org/).

We detected 8 novel variants predicted to be deleterious in 494 Chinese controls. There is a significant enrichment of novel deleterious missense variants detected in short stature patients when compared to the normal Chinese controls (p = 0.016 Fisher exact test). It is unclear if the inherited variants in Patients D and E are pathogenic given the lack of segregation with short stature in the family. Partial penetrance of these two inherited variants are possible. Based on the recently published guideline for variant interpretation [9], the two de novo variants are classified as likely pathogenic and the other two variants are of uncertain significance (see Additional file 4).

Discussion

High resolution array CGH enables the detection of small CNVs involving one gene or part of a gene. This approach allowed for the identification of candidate short stature genes. We scanned the whole genome for single CNVs in individual patients or overlapping CNVs with a single gene in the region of overlap in patients with short stature. We paid particular attention to de novo CNVs only present in patients and not in a control population. By this approach, we identified a chromatin-remodeling gene ARID1B as a novel short stature gene. ARID1B was the only gene in the region of overlap involving two deletions and one duplication. The two deletions were de novo. ARID1B has been identified as one of the causal genes for Coffin-Siris syndrome and it has also been associated with syndromic intellectual disability [10]. While growth retardation was mentioned as one of the features of Coffin-Sirissyndrome [11], this feature is currently under appreciated [12]. We then performed a comprehensive case review of the clinical features of all individuals carrying mutation in ARID1B regardless of their associated syndromes (Table 1). This genotype-driven approach revealed a significant association between short stature and mutations in ARID1B. Next, we further explored the possible contribution of ARID1B mutations to non-syndromic short stature by screening 48 short stature patients who did not have developmental delay or intellectual disability. As a result, we identified four novel missense variants in ARID1B including two de novo variants. The likelihood of a chance finding of two de novo variants in the same gene in 48 individuals is extremely small, indicating that these variants are likely causal of the patients’ short stature. Collectively, our data support the notion that ARID1B mutations cause growth retardation in syndromic patients and may also contribute to non-syndromic short stature.

Coffin-Siris syndrome and short stature

Recently, loss of function mutations in ARID1B were identified as causative for Coffin-Siris syndrome, a rare genetic condition characterized by growth deficiency, developmental delay, severe speech impairment, intellectual disability, and specific physical features including microcephaly, coarse facial features, hypertrichosis, hypoplastic or absent fifth fingernails or toenails and hypoplasia or agenesis of the corpus callosum [13]. Our patient A exhibited many features of Coffin-Siris but was not noted to have hypoplastic or absent fifth fingernails or toenails. Our patient B showed typical signs of Coffin-Siris syndrome but not patient C. All three patients exhibited short stature. We performed a comprehensive review on published cases with loss-of-function mutations in ARID1B (Table 1). Based on the available clinical information from the published literature, all patients showed developmental delay (70/70) and language impairment (63/63). Most of patients exhibited hypertonia (49/56), seizures (16/52), agenesis of corpus callosum (23/47), autism or autistic features (9/42) as well as dysmorphic features: low-set or abnormal-shaped ears (42/47), prominent nose (41/55), various eye-related features (51/64), hypertrichosis (38/51), coarse face/abnormal head shape (16/18), low hair line (9/11), and spinal/skeletal anomalies (10/12). Patients ascertained with Coffin-Siris syndrome also exhibited dysplastic nails.

Case review data showed that 34 % of patients with ARID1B mutations had short stature defined as height below -2 SD. The majority (90 %) had a height Z-score below -1 and none of the patients had above average height. The average Z score among patients for whom height data was available is -1.86. Thus, growth retardation and short stature is a common feature associated with mutations in ARID1B and Coffin-Siris syndrome.

Coffin-Siris syndrome is a nucleosome remodeling complex (SWI/SNF-SWI) disorder. Mutations in other genes involved with the SWI/SNF complex such as ARID1A, SMARCA2, SMARCA4, SMARCB1 and SMARCE1 are also responsible for Coffin-Siris syndrome [12]. Recent genotype-phenotype analysis indicated that short stature is a prominent feature in patients carrying mutations in those other SWI/SNF genes [14] as well. Among all the Coffin-Siris syndrome patients detected with mutations in those BAF-complex-related-genes (BRG1/brm-associated factor), 21 % of them (9/43) showed short stature. Additionally, 24 % of Coffin-Siris patients without identified mutations presented with short stature. Thus short stature is a common feature of Coffin-Siris syndrome.

ARID1B and non-syndromic short stature

We identified four novel missense variants among 48 individuals with idiopathic short stature not associated with developmental delay. These variants were not reported in 1000 genomes project database, dbSNP database, the ESP6500 dataset or ExAC database. Functional predictions suggest deleterious effect on protein for all four variants, although two of the variants were found in family members without short stature. All four variants were absent from 1100 ethnically matched controls. We found significantly fewer deleterious novel missense variants in age, gender, and ethnicity-matched controls than in short stature patients. Importantly, two of the variants were de novo changes not detected in parents and non-affected siblings. All four patients carrying ARID1B mutation showed no signs of Coffin-Siris syndrome, or developmental or mental deficits. ARID1B de novo mutations have been shown to contribute to the heritable complex traits, such as autism spectrum disorders (ASDs), although the effect size may be small [15]. We have not established the causal relationship between these mutations and short stature, but we postulate that ARID1B is also involved with idiopathic short stature in a similar manner.

Almost all 70 syndromic individuals carried loss-of-function ARID1B mutations which include genic deletions (n = 27), genic duplications (n = 2), nonsense mutations (n = 14), frame shift mutations (n = 21) and a translocation (n = 1). On the other hand, all variants identified in non-syndromic short stature are missense variants. Based on this finding, we postulate that while complete loss of the ARID1B gene product causes a syndrome that involves developmental delay, intellectual disability, dysmorphism and short stature, missense mutations may cause isolated short stature without developmental defects. Further testing of more non-syndromic short stature patient is warranted to validate such hypothesis.

Conclusions

In order to evaluate the association of ARID1B mutations with syndromic and non-syndromic short stature, we collected data from a total of 4411 patients who underwent clinical microarray testing at Boston Children’s Hospital, 48 non-syndromic short stature patients at Shanghai Children’s Medical Center and 70 patients reported in the literature with ARID1B gene mutations. By case-control study, retrospective genotype-phenotype analysis and ARID1B gene mutation screening, we found haploinsufficient mutations of ARID1B are associated with syndromic short stature in Coffin-Sirissyndromeor patients with intellectual disability. ARID1B mutations are also found to be associated with non-syndromic short stature. This finding supports the notion that chromatin-remodeling genes play an important role in human height regulation.

Ethics, consent and permissions

This study is reviewed and approved by ethics committee of Shanghai Children’s Medical Center【SCMC-IRB-K2013007】. All participants have signed a consent form, and all the information were obtained with appropriate consent based on the SCMC requirement.

Abbreviations

CNVs: 

Copy number variations

CMA: 

Chromosome microarray analysis

SD: 

Standard deviations

GWAS: 

Genome-wide association studies

GH: 

Growth hormone

MRO: 

Minimal region of overlap

PCR: 

Polymerase chain reaction

STR: 

Short tandem repeat

Declarations

Acknowledgements

We thank the support from the patients and their families. This study is further supported by the “the Program of Shanghai Committee of Science and Technology” from The Shanghai Municipal Science and Technology Commission (No. 124119a2601 and Shanghai Pujiang Talent Program No. 13PJ1406200, to YYG); Health Science grant from the social development branch of Pudong New District(PKJ2012-Y47 for YYG). AD is supported by a grant from the National Institute of Child Health and Human Development (5K23HD073351). YS is supported by grants from “Eastern Scholar” Fund and National Natural Science Foundation of China (No. 81371903).

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Authors’ Affiliations

(1)
Department of Pediatric Endocrinology/Genetics, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai Institute for Pediatric Research
(2)
Medical Genetics Department, Shanghai Children’s Medical Center, Shanghai Jiaotong University School of Medicine
(3)
Division of Endocrinology and Genetic Metabolism, Department of Internal Medicine, Shanghai Children’s Medical Center, Shanghai Jiaotong University School of Medicine
(4)
Division of Endocrinology and Division of Genetics, Children’s Hospital Boston
(5)
Program in Medical and Population Genetics, Metabolism Program, Broad Institute
(6)
Center for Basic and Translational Obesity Research, Children’s Hospital Boston
(7)
Division of Endocrinology, Cincinnati Children’s Hospital Medical Center
(8)
Department of Laboratory Medicine, Boston Children’s Hospital
(9)
Department of Pathology, Harvard Medical School
(10)
Claritas Genomics

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Copyright

© Yu et al. 2015

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