Faculty
QI Huayu
Title:Principle Investigator
Subject:
Email:qi_huayu@gibh.ac.cn
Address:No.190 Kaiyuan Road, Guangzhou Science Park, Luogang District, Guangzhou 510530,F204
Study/Work Experience

2007 – now

Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences/ Principal Investigator

2003 – 2007

Children’s Hospital, Harvard Medical School, Boston, USA /Post-Doc

Research Areas

Animal bodies are composed of various types of tissues and cells that perform physiological functions animals need in order to stay vital.  The development of an animal is therefore also the development of tissues and cells within an animal body.  In mammals, all lives start with the fusion of two highly specialized gametes, sperm and egg, in the process of fertilization that generates totipotent cells, the zygotes, which can develop into all tissue and cell types of the future animal.  Genetic defects occurred during gametes and embryo development can influence adult animals, and in human, cause human diseases.  Thus, studies of development of gametes and early embryos will not only help to understand fundamental biological questions but also provide us with better chances to conquer human diseases.

The overall research in my lab is to understand the developmental mechanisms of male gamete, the sperm, using mouse as the model system.  By applying different biological approaches, we aim to understand the molecular basis that underlies the development of mouse spermatozoa, mechanisms that control spermatogenesis.  In the meantime, regulation of pre-implantation embryogenesis and the relationships between early embryogenesis and the future development of animals are another line of our focus.  Insights gained from these studies will help to solve fundamental questions in developmental biology and open new windows for finding treatments of human diseases.

Our current research includes:

1) Molecular mechanisms that regulate mouse spermatogonial stem cells.  Spermatogonial stem cells give rise to mature spermatozoa throughout the adult life of an animal.  It is an ideal model to study stem cell biology and regeneration.  Using biochemical and cell biological approaches, as well as contemporary genetic and high-throughput methods, we wish to first learn the true identities of spermatogonial stem cells in their natural habitats and subsequently to dissect the molecular pathways that govern their maintenance and differentiation throughout the life of an animal, even during the regeneration when spermatogenic cells are injured by un-natural means.  We are currently investigating the roles of RNA binding proteins, AKT-mTORC1/2 signaling and translation regulatory pathways that may influence the self-renewal and proliferation of spermatogonial stem cells.  Some of the target genes are identified from gene expression profiling of mouse spermatogonial stem cells we conducted previously.

2) Translational regulation during spermiogenesis.  Post-meiotic development occupies one-third of spermatogenic process and proceeds without much active gene transcription.  The spatial-temporal regulation of protein synthesis that is required for sperm differentiation is a central mechanism that governs sperm development.  Through the study of sperm-specific proteins such as AKAP3, we wish to understand the molecular underpinnings that direct the regulatory signaling and molecular mechanisms that govern spermiogenesis as a whole. 

3) Molecular mechanisms of germ cell development share their roots at the beginning of animal’s life.  The analyses on molecular and cellular differentiation of pre-implantation embryos will bring us insights into how cells change their identities during development in order to fulfill physiological functions. 

These works are the necessary and first steps toward our future endeavors in understanding how animals utilize reproductive systems to perpetuate and improve lives and eventually comprehending the nature of our own.


Academic Performance
One Hundred Talent, Chinese Academy of Sciences, 2008

Representative Papers

1. Yang, L. Liao, J., Huang, H., Lee, T. L. and Qi, H.  Stage-specific regulation of undifferentiated spermatogonia by AKT1S1-mediated AKT-mTORC1 signaling during mouse spermatogenesis.  Developmental Biology 509: 11-27 (2024).  DOI: 10.1016/j.ydbio.2024.02.002.

2. Zou, Q., Yang, L. and Qi, H.  Protocol for isolation and proteostatic analysis of sub-populations of spermatogenic cells in mouse.  STAR Protocols May 14; 3(2): 101398 (2022).  DOI: 10.1016/j.xpro.2022.101398.

3. Shi, K., Yang, L., Zhuang, X., Zhang, L. and Qi, H.  Yeast Two-Hybrid Screen Identifies PKA-Rialpha Interacting Proteins during Mouse Spermiogenesis.  Genes (Basel) Nov 30; 12(12): 1941 (2021).  DOI: 10.3390/genes12121941.

4. Zou, Q., Yang, L., Shi, R., Qi, Y., Zhang, X. and Qi, H.  Proteostasis regulated by testis-specific ribosomal protein RPL39L maintains mouse spermatogenesis.  iScience Oct 30; 24(12): 103396 (2021).  DOI: 10.1016/j.isci.2021.103396.

5. Zou, Q. and H. Qi.  Deletion of ribosomal paralogs Rpl39 and Rpl39l compromises cell proliferation via protein synthesis and mitochondrial activity.  International Journal of Biochemistry and Cell Biology Oct; 139: 106070 (2021).  DOI: 10.1016/j.biocel.2021.106070.

6. Xu, K., Yang, L., Zhang, L. and Qi, H.  Lack of AKAP3 disrupts integrity of sub-cellular structure and proteome of mouse sperm and causes male sterility.  Development Jan 22; 147(2): dev18107 (2020).  DOI:10.1242/dev.181057.

7. Wu, Y., Xu, K and Qi, H.  Domain-functional analyses of PIWIL1 and PABPC1 indicate their synergistic roles in protein translation via 3’-UTRs of meiotic mRNAs.  Biology of Reproduction Oct 1; 99(4): 773-788 (2018).  DOI: 10.1093/biolre/ioy100.

8. Qi, H.  RNA-binding proteins in mouse male germline stem cells: a mammalian perspective.  Cell Regeneration (Lond) Feb 2; 5: 1 (2016).  DOI: 10.1186/s13619-015-0022-y.

9. Zheng, Z., Li H., Zhang, Q., Yang, L. and Qi, H.  Unequal distribution of 16S mtrRNA at the 2-cell stage regulates cell lineage allocations in mouse embryos.  Reproduction Apr; 151(4): 351-367 (2016).  DOI: 10.1530/REP-15-0301.

10. Xu, K., Yang, L., Zhao, D., Wu, Y., Qi, H.  AKAP3 synthesis is mediated by RNA binding proteins and PKA signaling during mouse spermiogenesis.  Biology Reproduction Jun; 90(6): 1-14 (2014).  DOI: 10.1095/bioreprod.113.116111.

11. Xu, K., Qi, H.  Sperm specific AKAP3 is a dual specificity anchoring protein that interacts with both protein kinase A regulatory subunits via conserved N-terminal amphipathic peptides.  Molecular Reproduction and Development Jul; 81(7): 595-607 (2014).  DOI: 10.1002/mrd.22329.

12. Yang, L., Wu, W. and Qi, H.  Gene expression profiling revealed specific spermaogonial stem cell genes in mouse.  Genesis Feb; 51(2): 83-96 (2013).  DOI:10.1002/dvg.22358.