综述

p53家族及其通路相关蛋白调节母性生殖的新功能

展开
  • 1. 昆明理工大学生命科学与技术学院, 衰老与肿瘤分子遗传实验室, 昆明 650500 2. 昆明市公安局刑事犯罪侦查支队, 昆明 650224 3. 中国科学院昆明动物研究所, 遗传资源与进化国家重点实验室, 昆明 650223

收稿日期: 2012-01-13

  修回日期: 2012-02-20

  网络出版日期: 2012-08-25

基金资助

国家自然科学基金项目(编号:30960152, 30871232, 31170735), 教育部新世纪优秀人才项目和遗传资源与进化国家重点实验室开放课题(编号:GREKF10-07)资助

The new function of p53 family and its pathway related proteins in female reproduction

Expand
  • 1. Laboratory of Molecular Genetics of Aging and Tumor, Faculty of Life Science and Technology, Kunming University of Science and Technology, Kunming 650500, China 2. Criminal Investigation Team, KunmingPublicSecurity Bureau, Kunming 650224, China 3. State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China

Received date: 2012-01-13

  Revised date: 2012-02-20

  Online published: 2012-08-25

摘要

p53是一种重要的抗癌基因, 同时它也是机体感受环境压力并进行相应调节的关键基因之一。最近的研究发现东亚人群p53 Arg72Pro受到冬季温度自然选择, 表明p53可能在生殖中发挥作用。同时, p53及其通路中的癌基因鼠双微体2(Murinedoubleminute2, Mdm2)、MdmXHausp(Herpesvirus-associated ubiquitin-specific protease)基因的单核苷酸多态性(Single nucleotide poly-morphisms, SNP)与女性生殖疾病易感性相关。P53蛋白通过其DNA结合区(DNA-binding domain, DBD)调控白血病抑制因子(Leukaemiainhibitory factor, LIF)表达, 从而影响胚胎植入过程, 实现其在母性生殖中的作用。p53通路中Mdm2、MdmXHausp可以调控P53蛋白的表达水平和活性, 同时还可以在胚胎植入时准确的调控p53的表达水平, 促进胚胎植入; P53家族成员P63、P73具有P53相似的DBD区, 但P63和P73是通过别的途径影响到母性生殖; 在卵母细胞受到射线或者化学损伤后, P63能促进其凋亡, 减少畸型的产生; P73能影响纺锤体复合物的组装, 而纺锤体复合物缺失将导致胚泡质量低下, 微管结合的动粒缺失和细胞非整倍性的增加。文章主要综述了p53家族、p53通路中的相关蛋白对母性生殖的影响, 为提高IVF-ET成功指出了新方法, 同时也为不明原因的不孕患者提供了新的诊断思路, 将有助于制定合理的个性化治疗不孕方案。

关键词: p53; LIF; SNP; p53通路; 胚胎植入

本文引用格式

朱晖,李安,余建华,向超杰,苏世达,黄磊,范豫杰,罗瑛,唐文如 . p53家族及其通路相关蛋白调节母性生殖的新功能[J]. 遗传, 2012 , 34(8) : 943 -949 . DOI: 10.3724/SP.J.1005.2012.00943

Abstract

p53 is an important tumor suppressor gene andone of the key genes in sensing and regulating responses to the environmental stress. Recent study showed that cold winter temperature naturally selectedp53 Arg72 in eastern Asian popu-lation, suggestingthat p53 playsa role in reproduction. It has also been reported that some SNPs of p53, Mdm2(Murine double minute 2), MdmX and Hausp (Herpes virus-associated ubiquitin-specific protease) in p53 pathway are associated with the risk of the women’s reproduction disorder. p53 regulates the LIF (leukaemia inhibitory factor) expression level by its DBD domain, and thus contributes to female reproduction by affecting the embryo implantation process. The MDM2, MDMX, and HAUSP proteins regulatesthelevel and activity of p53 protein, which are critical for the appropriate p53 response in the embryo implantation process. The members of p53 family, p63 and p73, also play roles in female reproduction through other pathways. p63 has been implicated as a major regulator of oocyte death following treatment with irradiation and chemotherapeutic drugs, which prevents fetal malformation. p73 regulates the formation of spindle assembly complex(SAC). The dysfunction of SAC results in poor blastocyst quality and defects in kinetochore–microtubule associations, which leads to aneuploidy. This review summarized the function of p53 family and its pathway related proteins in female reproduction, pointed out a new method in improving the success rate in IVF-ET, and provided a new diagnosis idea for unexplainedinfertile women. It will facilitate personalized strategies in the infertility therapy.

参考文献

[1] Atwal GS, Bond GL, Metsuyanim S, Papa M, Friedman E, Distelman-Menachem T, Ben Asher E, Lancet D, Ross DA, Sninsky J, White TJ, Levine AJ, Yarden R. Haplotype structure and selection of the MDM2 oncogene in humans. Proc Natl Acad Sci USA, 2007, 104(11): 4524-4529.

[2] Murphy ME. Polymorphic variants in the p53 pathway. Cell Death Differ, 2006, 13(6): 916-920.

[3] Kay C, Jeyendran RS, Coulam CB. p53 tumour suppressor gene polymorphism is associated with recurrent implantation failure. Reprod Biomed Online, 2006, 13(4): 492-496.

[4] Hu W, Feng Z, Teresky AK, Levine AJ. p53 regulates maternal reproduction through LIF. Nature, 2007, 450(7170): 721-724.

[5] Lin J, Wu X, Chen J, Chang A, Levine AJ. Functions of the p53 protein in growth regulation and tumor suppression. Cold Spring Harb Symp Quant Biol, 1994, 59: 215-223.

[6] Takahama Y, Ochiya T, Sasaki H, Baba-Toriyama H, Konishi H, Nakano H, Terada M. Molecular cloning and functional analysis of cDNA encoding a rat leukemia in-hibitory factor: towards generation of pluripotent rat em-bryonic stem cells. Oncogene, 1998, 16(24): 3189-3196.

[7] Menendez D, Inga A, Resnick MA. The expanding universe of p53 targets. Nat Rev Cancer, 2009, 9(10): 724-737.

[8] Feng Z, Zhang C, Kang HJ, Sun Y, Wang H, Naqvi A, Frank AK, Rosenwaks Z, Murphy ME, Levine AJ, Hu W. Regulation of female reproduction by p53 and its family members. FASEB J, 2011, 25(7): 2245-2255.

[9] Stewart CL, Kaspar P, Brunet LJ, Bhatt H, Gadi I, Kontgen F, Abbondanzo SJ. Blastocyst implantation depends on maternal expression of leukaemia inhibitory factor. Nature, 1992, 359(6390): 76-79.

[10] Cheng TC, Huang CC, Chen CI, Liu CH, Hsieh YS, Huang CY, Lee MS, Liu JY. Leukemia inhibitory factor antisense oligonucleotide inhibits the development of murine embryos at preimplantation stages. Biol Reprod, 2004, 70(5): 1270-1276.

[11] Fry RC. The effect of leukaemia inhibitory factor (LIF) on embryogenesis. Reprod Fertil Dev, 1992, 4(4): 449-458.

[12] Cheng JG, Rodriguez CI, Stewart CL. Control of uterine receptivity and embryo implantation by steroid hormone regulation of LIF production and LIF receptor activity: towards a molecular understanding of "the window of im-plantation". Rev Endocr Metab Disord, 2002, 3(2): 119- 126.

[13] Vogiagis D, Salamonsen LA, Sandeman RM, Squires TJ, Butt AR, Fry RC. Effect of immunisation against leukae-mia inhibitory factor on the establishment of pregnancy in sheep. Reprod Nutr Dev, 1997, 37(4): 459-468.

[14] Gearing DP, Thut CJ, VandeBos T, Gimpel SD, Delaney PB, King J, Price V, Cosman D, Beckmann MP. Leukemia inhibitory factor receptor is structurally related to the IL-6 signal transducer, gp130. EMBO J, 1991, 10(10): 2839-2848.

[15] Nakamura H, Kimura T, Ogita K, Nakamura T, Takemura M, Shimoya K, Koyama S, Tsujie T, Koyama M, Murata Y. NF-kappaB activation at implantation window of the mouse uterus. Am J Reprod Immunol, 2004, 51(1): 16-21.

[16] Bischof P, Haenggeli L, Campana A. Effect of leukemia inhibitory factor on human cytotrophoblast differentiation along the invasive pathway. Am J Reprod Immunol, 1995, 34(4): 225-230.

[17] Bamberger AM, Jenatschke S, Schulte HM, LoningT, Bamberger MC. Leukemia inhibitory factor (LIF) stimu-lates the human HLA-G promoter in JEG3 choriocarci-noma cells. J Clin Endocrinol Metab, 2000, 85(10): 3932-3936.

[18] Hirota Y, Daikoku T, Tranguch S, Xie H, Bradshaw HB, Dey SK. Uterine-specific p53 deficiency confers prema-ture uterine senescence and promotes preterm birth in mice. J Clin Invest, 2010, 120(3): 803-815.

[19] Feng Z, Zhang C, Kang HJ, Sun Y, Wang H, Naqvi A, Frank AK, Rosenwaks Z, Murphy ME, Levine AJ, Hu W. Regulation
文章导航

/