Mutant ZP1 in Familial Infertility

被引:122
作者
Huang, Hua-Lin [1 ,6 ]
Lv, Chao [1 ]
Zhao, Ying-Chun [6 ]
Li, Wen [1 ,2 ]
He, Xue-Mei [4 ]
Li, Ping [4 ]
Sha, Ai-Guo [5 ]
Tian, Xiao [3 ]
Papasian, Christopher J. [7 ]
Deng, Hong-Wen [6 ]
Lu, Guang-Xiu [1 ,2 ]
Xiao, Hong-Mei [1 ,2 ]
机构
[1] Cent S Univ, Inst Reprod & Stem Cell Engn, Changsha 410008, Hunan, Peoples R China
[2] Reprod & Genet Hosp CITIC Xiangya, Changsha, Hunan, Peoples R China
[3] First High Sch Changsha, Changsha, Hunan, Peoples R China
[4] Xiamen Maternal & Child Hlth Care Hosp, Xiamen, Peoples R China
[5] PLA Hosp 174, Xiamen, Peoples R China
[6] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Biostat & Bioinformat, New Orleans, LA USA
[7] Univ Missouri Kansas City, Sch Med, Kansas City, MO USA
基金
美国国家卫生研究院;
关键词
ZONA-PELLUCIDA GLYCOPROTEINS; FEMALE MICE; EGG; DOMAIN; FOLLICULOGENESIS; FERTILIZATION; PROTEINS; LACKING;
D O I
10.1056/NEJMoa1308851
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The human zona pellucida is composed of four glycoproteins (ZP1, ZP2, ZP3, and ZP4) and has an important role in reproduction. Here we describe a form of infertility with an autosomal recessive mode of inheritance, characterized by abnormal eggs that lack a zona pellucida. We identified a homozygous frameshift mutation in ZP1 in six family members. In vitro studies showed that defective ZP1 proteins and normal ZP3 proteins colocalized throughout the cells and were not expressed at the cell surface, suggesting that the aberrant ZP1 results in the sequestration of ZP3 in the cytoplasm, thereby preventing the formation of the zona pellucida around the oocyte. The zona pellucida is a clear, gelatinous matrix that surrounds the ovum and is essential to fertilization. Four sisters with primary infertility were found to harbor a mutation affecting one of the ZP proteins. Summary The human zona pellucida is composed of four glycoproteins (ZP1, ZP2, ZP3, and ZP4) and has an important role in reproduction. Here we describe a form of infertility with an autosomal recessive mode of inheritance, characterized by abnormal eggs that lack a zona pellucida. We identified a homozygous frameshift mutation in ZP1 in six family members. In vitro studies showed that defective ZP1 proteins and normal ZP3 proteins colocalized throughout the cells and were not expressed at the cell surface, suggesting that the aberrant ZP1 results in the sequestration of ZP3 in the cytoplasm, thereby preventing the formation of ...
引用
收藏
页码:1220 / 1226
页数:7
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