- Case report
- Open Access
A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature
BMC Medical Genomics volume 13, Article number: 126 (2020)
Proximal microdeletions on chromosome 15q25.2 are very rare, and are associated with neurodevelopmental delay, inguinal hernia, chest deformities, and anemia. The minimum length missed so far is 1.4 Mb. However, there were no cases reported till date on microdeletions at position q25.2 on chromosome 15 with premature ovarian failure (POF).
We herein reported a POF case characterized by short stature with only 0.447 Mb deletion on chromosome 15q25.2. The clinical and molecular characteristics in our patient showed the slightest clinical manifestations, with no clinical signs of neurodevelopmental delay, inguinal hernia, chest deformities, and anemia when compared to the previously reported cases. The microdeletions in our case included only 7 genes (HOMER2, FAM103A1, C15orf40, BTBD1, TM6SF1, HDGFRP3 and BNC1), and excluded the CPEB1 gene. Among these, the BNC1 gene is the only one that is known to be involved in reproduction. We hypothesized that the deletion of BNC1 gene in this patient led to haploinsufficiency, and consequently to POF.
The study of this case increased the knowledge on the molecular and phenotypic consequences of interstitial 15q25.2 deletion, emphasizing that BNC1 gene deletion in this region might contribute to POF.
Premature ovarian failure (POF) is a complex heterogeneous disease and a common genetic condition affecting 1 ~ 1.5% of women under 40 years of age, and the main manifestations include abnormal menstruation (amenorrhea, oligomenorrhea or frequent), elevated levels of gonadotropin (FSH > 25 U/L), and decreased female hormone level volatility. But in 50–80% of cases, POF is still classified as being idiopathic, suggesting a strong genetic association of the disease . In some cases, POF is caused by single-gene mutations that are inherited by autosomes or X-linked, while it is caused by chromosomal abnormalities, such as Turner syndrome, in few others . DNA microarray technology is used for detecting the submicroscopic copy number variation (CNV) revealing the pathogenesis of rare and complex diseases. The chromosome 15q25.2 region has a complex genomic structure and four low-copy repeats, which mediate non-allelic homologous recombination and result in the deletion of chromosome fragments . Till date, there are about 10 patients with proximal 15q25.2 microdeletions reported [3,4,5,6]. The clinical phenotypic features of these patients include retarded intellectual development, short stature, craniofacial deformities, congenital diaphragmatic hernia (CDH), Diamond-Blackfan anemia (DBA), and mental disorders. In addition, some rare phenotypes included cleft lip, dextrocardia, and obstructive sleep apnea [3,4,5,6,7,8]. The clinical phenotype of these patients showed close association with the genes present in the deletion region. However, there are few reports on 15q25.2 microdeletions and POF.
We herein reported a case with 15q25.2 microdeletions and compared this patient with the previously reported female cases to propose the possible candidate genes for POF based on the observed characteristics.
A 14-year-9-month-old female who is the only child of healthy and nonconsanguineous Chinese parents was referred to our hospital for investigation due to her short stature and lack of menstruation. At birth, her weight was 3100 g and length was 50 cm. She was born without any difficulty during delivery and her mental and motor abilities remained normal. She developed breasts when she was 13 years old but not menstruated yet. Physical examination revealed a height and weight of 143.9 cm (− 2.9SD) and 29.5 Kg (− 2.98SD), respectively. Karyotype analysis showed 46, XX. The breast development was stage B3 (with obvious enlargement and elevation of the whole breast) and pubic hair development was stage PH4 (the publc hair was long and dark and spread to the pubic region). The bone age is about 12 years old (Gruelich-Pyle). Pelvic ultrasound showed that the uterus size was about 2.5 cm × 2.1 cm × 2.7 cm; and the ovary was not clearly seen. There were no abnormalities detected in the ultrasound results of urinary and cardiovascular systems. The baseline levels of reproductive hormones revealed LH of 10.40 IU/L (normal: 0.00–15.26), FSH of 45.5 IU/L (normal: 0.19–7.97), and E2 of 18.3 pmol/L (normal: 26.9–254.6).
Based on the breast development, short stature, amenorrhea and undetected ovaries in the 14-year-9-month girl, the baseline levels of LH and FSH were significantly increased, diagnosing POF. DNA microarray analysis (CytoOneArray chip from Phalanx Biotech company) showed a 15q25.2 heterozygous microdeletion from 83,588,055 to 8,403,418 (Fig. 1). The deletion of 15q25.2 includes 7 genes: HOMER2, FAM103A1, C15orf40, BTBD1, TM6SF1, HDGFRP3 and BNC1. The aberration was neither detected in her father nor her mother, indicating that the deletion was arisen de novo. Genomic microdeletion involving chromosome 15q25.2 is a rare finding. Nevertheless, there are some reports of CNVs within this region that are associated with recognizable phenotypes. A search was performed in the NCBI and DECIPHER database (https://decipher.sanger.ac.uk/) and identified 7 patients carrying similar microdeletions. Figure 2 showed the size and location of the 15q25.2 deletion (chr15: 83588055–84,035,418) as compared to the published female cases.
Estrogen replacement therapy is generally used for patients with POF. However, the patient did not receive further treatment because of her parents’ concern regarding the side effects.
Discussion and conclusions
The chromosome 15q25.2 region has a complex genomic structure and four low-copy repeats that mediate non-allelic homologous recombination and result in deletion of chromosome fragments . The clinical phenotype of these patients is closely related to the genes present in the deleted regions. The clinical phenotypes mainly included mental retardation, short stature, craniofacial deformity, CDH, DBA, and mental disorders. In addition, all female patients have POF . Our patient presented with characteristics of short stature and ovarian dysplasia, without intellectual disability, anemia, structural malformation of the thorax and upper abdomen, venous thrombosis or other clinical manifestations. As reported previously, CPEB1 (cytoplasmic polyadenylation element-binding protein-1, OMIM 607342) is highly expressed in the brain and plays an important role in maintaining the production of mitochondrial ATP in nerve cells. Adaptor protein-3 (AP3) is a heterotetrameric vesicle-coat protein complex that constitutes AP3 complex subunit beta-2 (AP3B2, OMIM 602166) as a subunit of non-clathrin and clathrin-associated AP3, which plays a role in protein sorting in the late-Golgi/trans-Golgi network (TGN) and/or endosomes. AP3 is involved in the sorting of a subset of transmembrane proteins targeted to lysosomes and lysosome-related organelles. Therefore, AP3B2 is thought to have neuro-specific functions, such as releasing of the neurotransmitters. AP3 is a heterotetrameric vesicle-coat protein complex, and so deletion of CPEB1 gene and AP3B2 gene is related to the phenotype of neural abnormality, and our patient’s microdeletion does not include these two genes, explaining as to why she has no clinical manifestations of the nervous system. It is currently believed that deletion of RPS17L (OMIM 180472) gene might be responsible for the cause of anemia in patients with a proximal 15q25.2 microdeletion, and no loss of this gene has occurred in this patient. BTBD1 (protein 1 containing BTB/POZ domain, OMIM 608530), HDGFRP3 (hepatoma derived growth factor-associated protein 3, OMIM 616643) and BCN1 (basculin 1, OMIM 601930) played roles in cell proliferation . Wat et al.  have suggested that these genes were associated with short stature and developmental delay in patients with 15q25.2 deletion.
Hyon et al.  have reported three patients with 15q25.2 microdeletions that are associated with ovarian insufficiency. Their minimum common area (chr15:83223426 to 84,832,932) included 12 genes (CPEB1, AP3B2, FSD2, WHAMM, HOMER2, FAM103A1, C15orf40, BTBD1, TM6SF1, HDGFRP3, BNC1, SH3GL3), and the heterozygous deletion of CPEB1 genes was believed to be responsible for the early POF in females . The clinical features of female patients with 15q25.2 deletion are summarized in Table 1. However, the microdeletions in our patient included only 7 genes (HOMER2, FAM103A1, C15orf40, BTBD1, TM6SF1, HDGFRP3 and BNC1), which excluded the CPEB1 gene (chr15:83211951–83,317,612). Among these, the BNC1 gene is the only one known to be involved in reproduction. Human BNC1 gene encodes zinc finger protein basonuclin-1 . BNC1 is a zinc finger protein that is present in the epidermal basal cell layer and hair follicles. It is also abundantly found in the germ cells of the testes and ovaries. Furthermore, it plays a regulatory role in keratinocyte proliferation, and might also act as a regulator of rRNA transcription. Wittgenstein et al. believed that BNC1 gene is involved in oogenesis and is closely related to POF . BNC1 as a transcription factor is involved in oogenesis and folliculogenesis . Knockout of BNC1 gene resulted in female infertility . Recent study found that knockdown of BNC1 gene can reduce BMP15 and p-akt levels and inhibit meiosis in the oocytes. Female mouse models with Bnc1 mutation showed similar phenotype as that of POF . Zhang et al. have reported a familial POI caused by BNC1 mutation . The patients with POF reported by Hyon et al. missed both CPEB1 and BNC1 genes, and believed that CPEB1 is the cause of POF. However, the importance of BNC1 gene in the occurrence and development of POF was proved in our case. Therefore, we hypothesized that deletion of BNC1 gene in this patient led to haploinsufficiency and consequently to POF.
In summary, this study extended a relatively minor phenotype of the proximal deletion of chromosome 15q25.2 with POF, and revealed that BNC1 gene might be an important candidate gene for POF.
Availability of data and materials
The datasets analyzed during the current study are available from the corresponding author on reasonable request.
Premature ovarian failure
Chromosomal microarray chip
Copy number variation
Congenital diaphragmatic hernia
Laissue P. Aetiological coding sequence variants in non-syndromic premature ovarian failure: from genetic linkage analysis to next generation sequencing. Mol Cell Endocrinol. 2015;411:243–57.
Pouresmaeili F, Fazeli Z. Premature ovarian failure: a critical condition in the reproductive potential with various genetic causes. Int J Fertil Steril. 2014;8(1):1–12.
Mefford HC, Clauin S, Sharp AJ, Moller RS, Ullmann R, Kapur R, Pinkel D, Cooper GM, Ventura M, Ropers HH, et al. Recurrent reciprocal genomic rearrangements of 17q12 are associated with renal disease, diabetes, and epilepsy. Am J Hum Genet. 2007;81(5):1057–69.
Wagenstaller J, Spranger S, Lorenz-Depiereux B, Kazmierczak B, Nathrath M, Wahl D, Heye B, Glaser D, Liebscher V, Meitinger T, et al. Copy-number variations measured by single-nucleotide-polymorphism oligonucleotide arrays in patients with mental retardation. Am J Hum Genet. 2007;81(4):768–79.
Wat MJ, Enciso VB, Wiszniewski W, Resnick T, Bader P, Roeder ER, Freedenberg D, Brown C, Stankiewicz P, Cheung SW, et al. Recurrent microdeletions of 15q25.2 are associated with increased risk of congenital diaphragmatic hernia, cognitive deficits and possibly diamond--Blackfan anaemia. J Med Genet. 2010;47(11):777–81.
Cooper GM, Coe BP, Girirajan S, Rosenfeld JA, Vu TH, Baker C, Williams C, Stalker H, Hamid R, Hannig V, et al. A copy number variation morbidity map of developmental delay. Nat Genet. 2011;43(9):838–46.
Doelken SC, Seeger K, Hundsdoerfer P, Weber-Ferro W, Klopocki E, Graul-Neumann L. Proximal and distal 15q25.2 microdeletions-genotype-phenotype delineation of two neurodevelopmental susceptibility loci. Am J Med Genet A. 2013;161A(1):218–24.
Burgess T, Brown NJ, Stark Z, Bruno DL, Oertel R, Chong B, Calabro V, Kornberg A, Sanderson C, Kelly J, et al. Characterization of core clinical phenotypes associated with recurrent proximal 15q25.2 microdeletions. Am J Med Genet A. 2014;164A(1):77–86.
Hyon C, Mansour-Hendili L, Chantot-Bastaraud S, Donadille B, Kerlan V, Dode C, Jonard S, Delemer B, Gompel A, Reznik Y, et al. Deletion of CPEB1 gene: a rare but recurrent cause of premature ovarian insufficiency. J Clin Endocrinol Metab. 2016;101(5):2099–104.
McGuire MM, Bowden W, Engel NJ, Ahn HW, Kovanci E, Rajkovic A. Genomic analysis using high-resolution single-nucleotide polymorphism arrays reveals novel microdeletions associated with premature ovarian failure. Fertil Steril. 2011;95(5):1595–600.
Tseng H, Green H. Basonuclin: a keratinocyte protein with multiple paired zinc fingers. Proc Natl Acad Sci U S A. 1992;89(21):10311–5.
Tsuiko O, Noukas M, Zilina O, Hensen K, Tapanainen JS, Magi R, Kals M, Kivistik PA, Haller-Kikkatalo K, Salumets A, et al. Copy number variation analysis detects novel candidate genes involved in follicular growth and oocyte maturation in a cohort of premature ovarian failure cases. Hum Reprod. 2016;31(8):1913–25.
Assou S, Anahory T, Pantesco V, Le Carrour T, Pellestor F, Klein B, Reyftmann L, Dechaud H, De Vos J, Hamamah S. The human cumulus--oocyte complex gene-expression profile. Hum Reprod. 2006;21(7):1705–19.
Ma J, Zeng F, Schultz RM, Tseng H. Basonuclin: a novel mammalian maternal-effect gene. Development. 2006;133(10):2053–62.
Zhang D, Liu Y, Zhang Z, Lv P, Liu Y, Li J, Wu Y, Zhang R, Huang Y, Xu G, et al. Basonuclin 1 deficiency is a cause of primary ovarian insufficiency. Hum Mol Genet. 2018;27(21):3787–800.
This work was supported by grants from the National Natural Science Foundation of China (Grants No.11571309) and the key Research and Development Program of Zhejiang Province (2020C03121). The funder had no role in study design, data collection and analysis, decision to publish, or in the preparation of the manuscript.
Ethics approval and consent to participate
The Ethics approval was obtained from the Research Ethics Committee of the First Affiliated Hospital, College of Medical, Zhejiang University. The written consent to participate in the genetic testing was obtained from both the patient (the parents signed the form on behalf of their child) and her parents. We confirm that we have read the Journal’s position on issues involved in ethical publication and affirm that this report is consistent with those guidelines.
Consent for publication
Written informed consent was obtained from the patient’s parents for publication of this Case Report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Chen, Z., Chen, H., Yuan, K. et al. A 15q25.2 microdeletion phenotype for premature ovarian failure in a Chinese girl: a case report and review of literature. BMC Med Genomics 13, 126 (2020). https://doi.org/10.1186/s12920-020-00787-w
- Premature ovarian failure
- BCN1 gene