Corre Christina, Shinoda Gen, Zhu Hao, Cousminer Diana L, Crossman Christine, Bellissimo Christian, Goldenberg Anna, Daley George Q, Palmert Mark R
Division of EndocrinologyThe Hospital for Sick Children, 555 University Avenue, Toronto ON, M5G 1X8, CanadaDivision of Hematology/OncologyBoston Children's Hospital, Boston, Massachusetts, USADepartments of Pediatrics and Internal MedicineChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USAInstitute for Molecular MedicineFinland (FIMM), University of Helsinki, Helsinki, FinlandGenetics and Genome Biology ProgramThe Hospital for Sick Children, Toronto, Ontario, CanadaDepartment of Computer ScienceUniversity of Toronto, Toronto, Ontario, CanadaDepartments of Paediatrics and PhysiologyThe University of Toronto, Toronto, Ontario, Canada.
Division of EndocrinologyThe Hospital for Sick Children, 555 University Avenue, Toronto ON, M5G 1X8, CanadaDivision of Hematology/OncologyBoston Children's Hospital, Boston, Massachusetts, USADepartments of Pediatrics and Internal MedicineChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USAInstitute for Molecular MedicineFinland (FIMM), University of Helsinki, Helsinki, FinlandGenetics and Genome Biology ProgramThe Hospital for Sick Children, Toronto, Ontario, CanadaDepartment of Computer ScienceUniversity of Toronto, Toronto, Ontario, CanadaDepartments of Paediatrics and PhysiologyThe University of Toronto, Toronto, Ontario, Canada Division of EndocrinologyThe Hospital for Sick Children, 555 University Avenue, Toronto ON, M5G 1X8, CanadaDivision of Hematology/OncologyBoston Children's Hospital, Boston, Massachusetts, USADepartments of Pediatrics and Internal MedicineChildren's Research Institute, University of Texas Southwestern Medical Center, Dallas, Texas, USAInstitute for Molecular MedicineFinland (FIMM), University of Helsinki, Helsinki, FinlandGenetics and Genome Biology ProgramThe Hospital for Sick Children, Toronto, Ontario, CanadaDepartment of Computer ScienceUniversity of Toronto, Toronto, Ontario, CanadaDepartments of Paediatrics and PhysiologyThe University of Toronto, Toronto, Ontario, Canada.
J Endocrinol. 2016 Mar;228(3):179-91. doi: 10.1530/JOE-15-0360. Epub 2015 Dec 23.
Growth and pubertal timing differ in boys and girls. Variants in/near LIN28B associate with age at menarche (AAM) in genome-wide association studies and some AAM-related variants associate with growth in a sex-specific manner. Sex-specific growth patterns in response to Lin28b perturbation have been detected in mice, and overexpression of Lin28a has been shown to alter pubertal timing in female mice. To investigate further how Lin28a and Lin28b affect growth and puberty in both males and females, we evaluated Lin28b loss-of-function (LOF) mice and Lin28a gain-of-function (GOF) mice. Because both Lin28a and Lin28b can act via the conserved microRNA let-7, we also examined let-7 GOF mice. As reported previously, Lin28b LOF led to lighter body weights only in male mice while Lin28a GOF yielded heavier mice of both sexes. Let-7 GOF mice weighed less than controls, and males were more affected than females. Timing of puberty was assessed by vaginal opening (VO) and preputial separation (PS). Male Lin28b LOF and male let-7 GOF, but not female, mice displayed alteration of pubertal timing, with later PS than controls. In contrast, both male and female Lin28a GOF mice displayed late onset of puberty. Together, these data point toward a complex system of regulation by Lin28a, Lin28b, and let-7, in which Lin28b and let-7 can impact both puberty and growth in a sex-specific manner, raising the possibility that this pathway may contribute to differential regulation of male and female growth and puberty in humans.
男孩和女孩在生长发育及青春期启动时间上存在差异。在全基因组关联研究中,LIN28B基因内部或其附近的变异与初潮年龄(AAM)相关,一些与初潮年龄相关的变异以性别特异性方式与生长相关。在小鼠中已检测到对Lin28b干扰产生的性别特异性生长模式,并且已证明Lin28a的过表达会改变雌性小鼠的青春期启动时间。为了进一步研究Lin28a和Lin28b如何影响雄性和雌性的生长及青春期,我们评估了Lin28b功能丧失(LOF)小鼠和Lin28a功能获得(GOF)小鼠。由于Lin28a和Lin28b都可以通过保守的微小RNA let-7发挥作用,我们还检测了let-7功能获得(GOF)小鼠。如先前报道,Lin28b功能丧失仅导致雄性小鼠体重较轻,而Lin28a功能获得使两性小鼠体重均增加。Let-7功能获得小鼠体重比对照组轻,且雄性比雌性受影响更大。通过阴道开口(VO)和包皮分离(PS)评估青春期启动时间。雄性Lin28b功能丧失小鼠和雄性let-7功能获得小鼠(而非雌性)的青春期启动时间出现改变,包皮分离时间比对照组晚。相反,雄性和雌性Lin28a功能获得小鼠均出现青春期启动延迟。总之,这些数据表明存在一个由Lin28a、Lin28b和let-7组成的复杂调控系统,其中Lin28b和let-7可以以性别特异性方式影响青春期和生长,这增加了该通路可能参与人类男性和女性生长及青春期差异调节的可能性。