The goal of this project is to elucidate the mechanism of epigenetic programming in germ cells, especially focusing on the roles of DNA damage response pathways in sex chromosome inactivation. Germ cells are capable of unique epigenetic programming which is required for sexual reproduction. A better understanding of the epigenetic program in germ cells will illuminate various reproductive issues underlying infertility and birth defects. When germ cells undergo male meiosis to generate haploid sperm, X and Y chromosomes go through a distinct epigenetic program different from autosomes. At the pachytene stage of meiosis, the genes on the X and Y are epigenetically silenced in a process called meiotic sex chromosome inactivation (MSCI). The entire X and Y chromosomes form a chromatin domain, known as the XY body, which is distinct from autosome regions. The XY body is marked by various chromosome-wide epigenetic modifications, which presumably maintain MSCI. My postdoctoral work revealed that sex chromosome inactivation is maintained even after meiosis, and implicated epigenetic inheritance in spermiogenesis and the embryonic development of the next generation. In this proposal, we aim to dissect the molecular basis of epigenetic silencing of sex chromosomes. An intriguing link between epigenetic silencing of sex chromosomes and components involved in DNA damage response (DDR) pathways has been suggested. Cytological evidence shows that various components involved in DDR pathways accumulate on the X and Y at the onset of MSCI. Based on our preliminary studies using mouse models defective for DDR pathways, we hypothesize that DDR pathways are adapted to initiate and maintain chromosome-wide silencing of sex chromosomes in germ cells. We will investigate the role of DDR pathways in MSCI by:
(Aim 1) determining how chromosome-wide silencing is initiated;
(Aim 2) dissecting the genetic pathways that coordinate potential downstream pathways;
and (Aim 3) determining how epigenetic modifications on sex chromosomes are established to maintain inactivation. The proposed study in germ cells will potentially reveal a link between DDR pathways and epigenetic programming that can be generalized to somatic cells.

Public Health Relevance

The mouse models in the proposed study exhibit male reproductive failure, indicating this research will identify mechanisms associated with male infertility. Because epigenetic defects in germ cells may affect embryonic development, the proposed study has significant relevance to the causes of birth defects. Also, identifying steps involved in the epigenetic silencing of sex chromosomes during male meiosis will lead to an understanding of the genetic cause of sex-linked aneuploidy, which results in Turner syndrome (XO) and Klinefelter's syndrome (XXY).

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM098605-03
Application #
8516535
Study Section
Cellular, Molecular and Integrative Reproduction Study Section (CMIR)
Program Officer
Carter, Anthony D
Project Start
2011-08-01
Project End
2016-07-31
Budget Start
2013-08-01
Budget End
2014-07-31
Support Year
3
Fiscal Year
2013
Total Cost
$279,049
Indirect Cost
$96,664
Name
Cincinnati Children's Hospital Medical Center
Department
Type
DUNS #
071284913
City
Cincinnati
State
OH
Country
United States
Zip Code
45229
Maezawa, So; Hasegawa, Kazuteru; Yukawa, Masashi et al. (2018) Polycomb protein SCML2 facilitates H3K27me3 to establish bivalent domains in the male germline. Proc Natl Acad Sci U S A 115:4957-4962
Sakashita, Akihiko; Yeh, Yu-Han V; Namekawa, Satoshi H et al. (2018) Epigenomic and single-cell profiling of human spermatogonial stem cells. Stem Cell Investig 5:11
Maezawa, So; Hasegawa, Kazuteru; Alavattam, Kris G et al. (2018) SCML2 promotes heterochromatin organization in late spermatogenesis. J Cell Sci 131:
Abe, Hironori; Alavattam, Kris G; Kato, Yasuko et al. (2018) CHEK1 coordinates DNA damage signaling and meiotic progression in the male germline of mice. Hum Mol Genet 27:1136-1149
Maezawa, So; Alavattam, Kris G; Tatara, Mayu et al. (2018) A rapidly evolved domain, the SCML2 DNA-binding (SDB) repeats, contributes to chromatin binding of mouse SCML2. Biol Reprod :
Adams, Shannel R; Maezawa, So; Alavattam, Kris G et al. (2018) RNF8 and SCML2 cooperate to regulate ubiquitination and H3K27 acetylation for escape gene activation on the sex chromosomes. PLoS Genet 14:e1007233
Maezawa, So; Yukawa, Masashi; Alavattam, Kris G et al. (2018) Dynamic reorganization of open chromatin underlies diverse transcriptomes during spermatogenesis. Nucleic Acids Res 46:593-608
Maezawa, So; Hasegawa, Kazuteru; Yukawa, Masashi et al. (2017) Polycomb directs timely activation of germline genes in spermatogenesis. Genes Dev 31:1693-1703
Zhang, Tingting; Du, Wei; Wilson, Andrew F et al. (2017) Fancd2 in vivo interaction network reveals a non-canonical role in mitochondrial function. Sci Rep 7:45626
Alavattam, Kris G; Kato, Yasuko; Sin, Ho-Su et al. (2016) Elucidation of the Fanconi Anemia Protein Network in Meiosis and Its Function in the Regulation of Histone Modifications. Cell Rep 17:1141-1157

Showing the most recent 10 out of 27 publications