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akaturk Akademik ölçüm

Makale detayı · 2019 · article

PPP2R3C gene variants cause syndromic 46,XY gonadal dysgenesis and impaired spermatogenesis in humans

ISSN0804-4643
YÖKSİS OpenAlex Açık erişim · bronze
Yıl2019
Atıf31OpenAlex
Atıf26Semantic Scholar · 3 etkili
Yüzdelik%78,5
FWCI1,241,00 = dünya ortalaması
Scopus (SJR)Q1
WoS (JCR)Q1

Veri kaynağı ayrımı

  • YÖKSİSYÖKSİS makale kaydı
  • YÖKSİS dergi adıEuropean Journal of Endocrinology
  • Katalog eşleşmesi (ISSN)European Journal of Endocrinology
  • OpenAlexOpenAlex zenginleştirmesi (özet, atıf, konular)
  • Semantic Scholaratıf sayısı (OpenAlex ile birleştirilmez)

Özet

OpenAlex İngilizce

Context Most of the knowledge on the factors involved in human sexual development stems from studies of rare cases with disorders of sex development. Here, we have described a novel 46, XY complete gonadal dysgenesis syndrome caused by homozygous variants in PPP2R3C gene. This gene encodes B″gamma regulatory subunit of the protein phosphatase 2A (PP2A), which is a serine/threonine phosphatase involved in the phospho-regulation processes of most mammalian cell types. PPP2R3C gene is most abundantly expressed in testis in humans, while its function was hitherto unknown. Patients and methods Four girls from four unrelated families with 46, XY complete gonadal dysgenesis were studied using exome or Sanger sequencing of PPP2R3C gene. In total, four patients and their heterozygous parents were investigated for clinical, laboratory, immunohistochemical and molecular characteristics. Results We have identified three different homozygous PPP2R3C variants, c.308T>C (p.L103P), c.578T>C (p.L193S) and c.1049T>C (p.F350S), in four girls with 46, XY complete gonadal dysgenesis. Patients also manifested a unique syndrome of extragonadal anomalies, including typical facial gestalt, low birth weight, myopathy, rod and cone dystrophy, anal atresia, omphalocele, sensorineural hearing loss, dry and scaly skin, skeletal abnormalities, renal agenesis and neuromotor delay. We have shown a decreased SOX9-Phospho protein expression in the dysgenetic gonads of the patients with homozygous PPP2R3C variants suggesting impaired SOX9 signaling in the pathogenesis of gonadal dysgenesis. Heterozygous males presented with abnormal sperm morphology and impaired fertility. Conclusion Our findings suggest that PPP2R3C protein is involved in the ontogeny of multiple organs, especially critical for testis development and spermatogenesis. PPPR3C provides insight into pathophysiology, as well as emerging as a potential therapeutic target for male infertility.

Konular

Atıflar

OpenAlex cited_by_count. WoS veya Scopus atıf sayısı değildir; o kaynaklar için ayrı kolon yoktur.

31atıfOpenAlex · cited_by_count (önbellek / veritabanı)

Yerel katalogda bu makaleye atıf yapan 2 yayın (OpenAlex referans eşleşmesi; tam dünya listesi değildir).

  1. 2022 Expanding The Spectrum of Syndromic PPP2R3C‐related XY Gonadal Dysgenesis to XX Gonadal DysgenesisAtıf 9 · OpenAlex
  2. 2026 Phenotype-Driven Whole-Exome Sequencing Reanalysis Identifies a Homozygous PPP2R3C Variant in Syndromic 46,XY and 46,XX Gonadal Dysgenesis: Case Report and Review of the LiteratureAtıf 0 · OpenAlex

Yazarlar

16
  1. TÜLAY GÜRAN MARMARA ÜNİVERSİTESİ 1
  2. GÖZDE YEŞİL SAYIN 2
  3. Serap Turan 3
  4. ZEYNEP ATAY 4
  5. EMİNE BOZKURTLAR 5
  6. AghaRza Aghayev 6
  7. Sinem Gül 7
  8. İLKER TİNAY İSTANBUL ATLAS ÜNİVERSİTESİ 8
  9. Başak Aru YEDİTEPE ÜNİVERSİTESİ 9
  10. Sema Arslan 10
  11. M Kutay Koroglu 11
  12. FERİHA ERCAN MARMARA ÜNİVERSİTESİ 12
  13. Gulderen Y Demirel 13
  14. ŞİRİN FUNDA EREN İSTANBUL KENT ÜNİVERSİTESİ 14
  15. Betul Karademir 15
  16. ABDULLAH BEREKET MARMARA ÜNİVERSİTESİ 16