Epigenetic Patterns Maintained in Early Caenorhabditis elegans Embryos Can Be Established by Gene Activity in the Parental Germ Cells

被引:56
作者
Arico, Jackelyn K. [1 ,2 ]
Katz, David J. [1 ]
van der Vlag, Johan [3 ]
Kelly, William G. [1 ]
机构
[1] Emory Univ, Rollins Res Ctr, Dept Biol, Atlanta, GA 30322 USA
[2] Emory Univ, Grad Program Biochem & Cell & Dev Biol, Atlanta, GA 30322 USA
[3] Radboud Univ Nijmegen, Med Ctr, Dept Nephrol, Nephrol Res Lab,Nijmegen Ctr Mol Life Sci, NL-6525 ED Nijmegen, Netherlands
关键词
IMPRINTED X-INACTIVATION; HISTONE H3 METHYLATION; LINE DEVELOPMENT; CENP-A; CHROMOSOME; CHROMATIN; MOUSE; POLYCOMB; PROTEIN; EXPRESSION;
D O I
10.1371/journal.pgen.1001391
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学];
摘要
Epigenetic information, such as parental imprints, can be transmitted with genetic information from parent to offspring through the germ line. Recent reports show that histone modifications can be transmitted through sperm as a component of this information transfer. How the information that is transferred is established in the parent and maintained in the offspring is poorly understood. We previously described a form of imprinted X inactivation in Caenorhabditis elegans where dimethylation on histone 3 at lysine 4 (H3K4me2), a mark of active chromatin, is excluded from the paternal X chromosome (Xp) during spermatogenesis and persists through early cell divisions in the embryo. Based on the observation that the Xp (unlike the maternal X or any autosome) is largely transcriptionally inactive in the paternal germ line, we hypothesized that transcriptional activity in the parent germ line may influence epigenetic information inherited by and maintained in the embryo. We report that chromatin modifications and histone variant patterns assembled in the germ line can be retained in mature gametes. Furthermore, despite extensive chromatin remodeling events at fertilization, the modification patterns arriving with the gametes are largely retained in the early embryo. Using transgenes, we observe that expression in the parental germline correlates with differential chromatin assembly that is replicated and maintained in the early embryo. Expression in the adult germ cells also correlates with more robust expression in the somatic lineages of the offspring. These results suggest that differential expression in the parental germ lines may provide a potential mechanism for the establishment of parent-of-origin epigenomic content. This content can be maintained and may heritably affect gene expression in the offspring.
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页数:15
相关论文
共 72 条
[51]
PURIFICATION OF THE CENTROMERE-SPECIFIC PROTEIN CENP-A AND DEMONSTRATION THAT IT IS A DISTINCTIVE HISTONE [J].
PALMER, DK ;
ODAY, K ;
TRONG, HL ;
CHARBONNEAU, H ;
MARGOLIS, RL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (09) :3734-3738
[52]
THE CENTROMERE SPECIFIC HISTONE CENP-A IS SELECTIVELY RETAINED IN DISCRETE FOCI IN MAMMALIAN SPERM NUCLEI [J].
PALMER, DK ;
ODAY, K ;
MARGOLIS, RL .
CHROMOSOMA, 1990, 100 (01) :32-36
[53]
The Histone H3K36 Methyltransferase MES-4 Acts Epigenetically to Transmit the Memory of Germline Gene Expression to Progeny [J].
Rechtsteiner, Andreas ;
Ercan, Sevinc ;
Takasaki, Teruaki ;
Phippen, Taryn M. ;
Egelhofer, Thea A. ;
Wang, Wenchao ;
Kimura, Hiroshi ;
Lieb, Jason D. ;
Strome, Susan .
PLOS GENETICS, 2010, 6 (09)
[54]
A global profile of germline gene expression in C-elegans [J].
Reinke, V ;
Smith, HE ;
Nance, J ;
Wang, J ;
Van Doren, C ;
Begley, R ;
Jones, SJM ;
Davis, EB ;
Scherer, S ;
Ward, S ;
Kim, SK .
MOLECULAR CELL, 2000, 6 (03) :605-616
[55]
X inactivation in the mouse embryo deficient for Dnmt1: Distinct effect of hypomethylation on imprinted and random X inactivation [J].
Sado, T ;
Fenner, MH ;
Tan, SS ;
Tam, P ;
Shioda, T ;
Li, E .
DEVELOPMENTAL BIOLOGY, 2000, 225 (02) :294-303
[56]
De novo DNA methylation is dispensable for the initiation and propagation of X chromosome inactivation [J].
Sado, T ;
Okano, M ;
Li, E ;
Sasaki, H .
DEVELOPMENT, 2004, 131 (05) :975-982
[57]
Transcriptional and Developmental Functions of the H3.3 Histone Variant in Drosophila [J].
Sakai, Akiko ;
Schwartz, Brian E. ;
Goldstein, Sara ;
Ahmad, Kami .
CURRENT BIOLOGY, 2009, 19 (21) :1816-1820
[58]
Genome regulation by polycomb and trithorax proteins [J].
Schuettengruber, Bernd ;
Chourrout, Daniel ;
Vervoort, Michel ;
Leblanc, Benjamin ;
Cavalli, Giacomo .
CELL, 2007, 128 (04) :735-745
[59]
Seydoux G, 1997, DEVELOPMENT, V124, P2191
[60]
SEYDOUX G, 1994, DEVELOPMENT, V120, P2823