A Twist between ROS and Sperm-Mediated Intergenerational Epigenetic Inheritance
2020; Elsevier BV; Volume: 78; Issue: 3 Linguagem: Inglês
10.1016/j.molcel.2020.04.003
ISSN1097-4164
Autores Tópico(s)Genetics, Aging, and Longevity in Model Organisms
ResumoYoshida et al., 2020Yoshida K. Maekawa T. Ly N.H. Fujita S.I. Muratani M. Ando M. Katou Y. Araki H. Miura F. Shirahige K. et al.ATF7-Dependent Epigenetic Changes Are Required for the Intergenerational Effect of a Paternal Low-Protein Diet.Molecular Cell. 2020; 78 (this issue): 445-458Abstract Full Text Full Text PDF Scopus (11) Google Scholar report in this issue of Molecular Cell that a paternal low-protein diet elevates ROS in the testicular germ cells, altering ATF7 activity and H3K9me2 abundance on target genes, including tRNA loci. These changes are maintained in spermatozoa, regulating tsRNA biogenesis, and together transmit intergenerational effects. Yoshida et al., 2020Yoshida K. Maekawa T. Ly N.H. Fujita S.I. Muratani M. Ando M. Katou Y. Araki H. Miura F. Shirahige K. et al.ATF7-Dependent Epigenetic Changes Are Required for the Intergenerational Effect of a Paternal Low-Protein Diet.Molecular Cell. 2020; 78 (this issue): 445-458Abstract Full Text Full Text PDF Scopus (11) Google Scholar report in this issue of Molecular Cell that a paternal low-protein diet elevates ROS in the testicular germ cells, altering ATF7 activity and H3K9me2 abundance on target genes, including tRNA loci. These changes are maintained in spermatozoa, regulating tsRNA biogenesis, and together transmit intergenerational effects. Increasing evidence demonstrates that unhealthy paternal nutritional status, such as a high-fat, high-sugar, or low-protein diet in mammals can induce non-DNA sequence-based epigenetic changes in the sperm and cause metabolic disorders in the offspring (Zhang et al., 2019Zhang Y. Shi J. Rassoulzadegan M. Tuorto F. Chen Q. Sperm RNA code programmes the metabolic health of offspring.Nat. Rev. Endocrinol. 2019; 15: 489-498Crossref PubMed Scopus (52) Google Scholar). However, a clear mechanism responsible for this intergenerational epigenetic inheritance phenomenon remains lacking. An interplay between histone marks, transcriptional activity, and small non-coding RNAs (sncRNAs) in the germ cell was anticipated to underlie such phenomena in mammals, as has been found in animals such as worms and flies. In this issue of Molecular Cell, Yoshida and colleagues report that a paternal low-protein diet (pLPD) elevates reactive oxygen species (ROS) in the mouse testicular germ cells (TGCs), altering transcription factor binding activity and associated histone marks that are maintained in spermatozoa, along with altered sperm sncRNA biogenesis, which may together transmit intergenerational effects. The present work (Yoshida et al., 2020Yoshida K. Maekawa T. Ly N.H. Fujita S.I. Muratani M. Ando M. Katou Y. Araki H. Miura F. Shirahige K. et al.ATF7-Dependent Epigenetic Changes Are Required for the Intergenerational Effect of a Paternal Low-Protein Diet.Molecular Cell. 2020; 78 (this issue): 445-458Abstract Full Text Full Text PDF Scopus (11) Google Scholar) extends from the lab’s previous studies in a fly model in which they found that environmental stresses in Drosophila can induce phosphorylation of ATF-2 (a mammalian ATF7 homolog), resulting in decreased H3K9me2 levels and altered heterochromatic status that are transmitted to the offspring (Seong et al., 2011Seong K.H. Li D. Shimizu H. Nakamura R. Ishii S. Inheritance of stress-induced, ATF-2-dependent epigenetic change.Cell. 2011; 145: 1049-1061Abstract Full Text Full Text PDF PubMed Scopus (197) Google Scholar). To explore whether ATF7 plays a similar role in mammalian sperm-induced intergenerational epigenetic inheritance, the authors chose a pLPD mouse model that has been reported to induce intergenerational effects in F1 offspring, manifested by altered liver gene expression (Carone et al., 2010Carone B.R. Fauquier L. Habib N. Shea J.M. Hart C.E. Li R. Bock C. Li C. Gu H. Zamore P.D. et al.Paternally induced transgenerational environmental reprogramming of metabolic gene expression in mammals.Cell. 2010; 143: 1084-1096Abstract Full Text Full Text PDF PubMed Scopus (756) Google Scholar). They first repeated the paternal LPD versus control diet (CD) treatment and indeed observed altered liver gene expression in the F1 offspring from the LPD-treated sires (Figure 1A). Next, the authors applied this paternal LPD versus CD model in an Atf7+/− mutant background and tracked the liver gene expression pattern in the F1 offspring as a readout for the intergenerational effects, from which they showed two interesting lines of findings and raised new questions along the way. First, they found that the F1 Atf7+/− offspring from the Atf7+/− sires, regardless of sire’s diet (LPD versus CD), showed a similar liver gene expression pattern largely overlapping with the F1 Atf7+/+ offspring from the wild-type Atf7+/+ LPD sires (Figure 1A). This phenomenon can be partially explained by their data that pLPD elevated the ROS in TGCs, which increased the phosphorylation of ATF7 by p38 and induced ATF7 release from its target; these changes in F0 Atf7+/+ males may mimic the deletion (dosage) effect of Atf7+/−. Supporting this idea, the authors found that the H3K9me2 abundance in TGCs was similarly decreased in the Atf7+/+-LPD, Atf7+/−-CD, and Atf7+/−-LPD groups comparing to the Atf7+/+-CD group. They further validated the altered ATF7 binding and H3K9me2 coverage in a set of metabolic-related genes in TGCs by ChIP-qPCR. Importantly, the change in H3K9me2 abundance on these genes was maintained in the mature sperm (spermatozoa). Notably, although ATF7 recruits both H3K9 di- and tri-methyltransferases, the overall H3K9me3 abundance in spermatozoa were not changed (Figure 1B). These data suggest a scenario in which the pLPD-ROS-p38-ATF7 axis generates a signature of histone marks on the Aft7(+) sperm from pLPD-exposed wild-type Atf7+/+ TGCs, similar to that of the Atf7(−) sperm from Atf7+/− TGCs (regardless of LPD or CD). This signature of histone marks might be responsible for programming embryo development, in that they induce the altered liver gene expression pattern in the F1 offspring. According to Yoshida et al., this intergenerational effect is most likely via an indirect mechanism through cascade regulation during development rather than by direct maintenance of H3K9me2 from sperm into the liver, due to the limited overlap of altered genes. The altered liver gene expression in F1 Atf7+/− offspring may also be due in part to the lack of one Atf7 allele in the liver cells. Nonetheless, these data showed how an epigenetic mark generated during spermatogenesis upon environmental stress can be maintained in spermatozoa, which may stand as a general mechanism in addition to the recent idea that sperm can gain exosomal information during epididymal transition (Zhang et al., 2019Zhang Y. Shi J. Rassoulzadegan M. Tuorto F. Chen Q. Sperm RNA code programmes the metabolic health of offspring.Nat. Rev. Endocrinol. 2019; 15: 489-498Crossref PubMed Scopus (52) Google Scholar). The second finding is more puzzling. The authors found that the F1 Atf7+/+ offspring from the F0 Atf7+/− sires under LPD versus CD showed substantially diminished changes in liver gene expression patterns compared to the distinct patterns between F1 Atf7+/+ offspring from the F0 Atf7+/+ sires under LPD versus CD (Figure 1A). That is, the differential gene expression signature tends to become assimilated toward an intermediate state. Since the Atf7(+) sperm derived from Atf7+/+-LPD, Atf7+/−-CD, and Atf7+/−-LPD TGCs may have similar H3K9me2 status, the differential effects in F1 are difficult to explain by simply considering the perspective of histone marks. In particular, why did the deletion of one Atf7 allele (Atf7+/−) in addition to pLPD exposure attenuate the abnormal liver gene expression, instead of enhancing the effect? One possible explanation is that beyond the effects of histone marks, Atf7+/− TGCs may generate additional (mobile) molecules that are inherited by Atf7(+) sperm (e.g., sncRNAs), which may act in trans to program embryo development. For example, the abnormal non-coding RNAs generated in the Kit+/− heterozygotic testis can be carried by the wild-type Kit(+) sperm to change the offspring’s phenotype as a case of paramutation in mice (Rassoulzadegan et al., 2006Rassoulzadegan M. Grandjean V. Gounon P. Vincent S. Gillot I. Cuzin F. RNA-mediated non-mendelian inheritance of an epigenetic change in the mouse.Nature. 2006; 441: 469-474Crossref PubMed Scopus (646) Google Scholar). Indeed, Yoshida et al. have found that the Atf7+/− TGCs showed altered transcriptional activities on a set of tRNAs compared to Atf7+/+ TGCs, partially due to differential H3K9me2 coverage; and that the spermatozoa from Atf7+/− males showed altered levels of tRNA-derived small RNAs (tsRNAs), some of which respond differently to LPD versus CD (Figure 1B). The altered tsRNAs in Atf7(+) sperm from Atf7+/− TGCs may exert an “assimilating” effect that, on the one hand, makes the Atf7(+) sperm from Atf7+/−-CD males “less normal,” while making the Atf7(+) sperm from Atf7+/−-LPD males “less abnormal,” thus resulting in a loss of gene expression distinction in the F1 offspring (Figure 1A). This scenario, while intriguing, is largely speculative because how the tsRNA may alter F1 gene expression via embryo development is thus far unclear, although injection of tsRNA-enriched sperm RNA fractions has been shown to induce metabolic phenotypes in the offspring (Chen et al., 2016Chen Q. Yan M. Cao Z. Li X. Zhang Y. Shi J. Feng G.H. Peng H. Zhang X. Zhang Y. et al.Sperm tsRNAs contribute to intergenerational inheritance of an acquired metabolic disorder.Science. 2016; 351: 397-400Crossref PubMed Scopus (562) Google Scholar). tsRNAs may regulate the establishment of histone marks and transcriptional and translational machinery in the early embryo, which are key questions awaiting to be addressed. The authors also noticed that the change of some tRNAs in TGCs does not match that of their corresponding tsRNAs in spermatozoa. This could be a result of complicated regulation of sncRNA biogenesis in sperm by ROS: 1) ROS regulate the p38-ATF7-H3K9me2 axis to alter tRNA transcription. 2) ROS mediate the cleavage of tRNA into tsRNAs (Thompson and Parker, 2009Thompson D.M. Parker R. Stressing out over tRNA cleavage.Cell. 2009; 138: 215-219Abstract Full Text Full Text PDF PubMed Scopus (269) Google Scholar), which depends on factors including tRNA modifications (Zhang et al., 2018Zhang Y. Zhang X. Shi J. Tuorto F. Li X. Liu Y. Liebers R. Zhang L. Qu Y. Qian J. et al.Dnmt2 mediates intergenerational transmission of paternally acquired metabolic disorders through sperm small non-coding RNAs.Nat. Cell Biol. 2018; 20: 535-540Crossref PubMed Scopus (133) Google Scholar), the specific RNases, and the compartmentalization of tRNAs (e.g., sperm head versus mitochondria) (Nätt et al., 2019Nätt D. Kugelberg U. Casas E. Nedstrand E. Zalavary S. Henriksson P. Nijm C. Jäderquist J. Sandborg J. Flinke E. et al.Human sperm displays rapid responses to diet.PLoS Biol. 2019; 17: e3000559Crossref Scopus (39) Google Scholar). ROS also induce rRNA cleavage into rRNA-derived small RNAs (rsRNAs) (Thompson and Parker, 2009Thompson D.M. Parker R. Stressing out over tRNA cleavage.Cell. 2009; 138: 215-219Abstract Full Text Full Text PDF PubMed Scopus (269) Google Scholar), and sperm rsRNAs are similarly altered by paternal diet and may function together with tsRNAs (Nätt et al., 2019Nätt D. Kugelberg U. Casas E. Nedstrand E. Zalavary S. Henriksson P. Nijm C. Jäderquist J. Sandborg J. Flinke E. et al.Human sperm displays rapid responses to diet.PLoS Biol. 2019; 17: e3000559Crossref Scopus (39) Google Scholar, Zhang et al., 2018Zhang Y. Zhang X. Shi J. Tuorto F. Li X. Liu Y. Liebers R. Zhang L. Qu Y. Qian J. et al.Dnmt2 mediates intergenerational transmission of paternally acquired metabolic disorders through sperm small non-coding RNAs.Nat. Cell Biol. 2018; 20: 535-540Crossref PubMed Scopus (133) Google Scholar). 3) ROS impact broadly on the quality of sperm nucleus involving DNA methylation and DNA damage (Drevet and Aitken, 2020Drevet J.R. Aitken R.J. Oxidation of Sperm Nucleus in Mammals: A Physiological Necessity to Some Extent with Adverse Impacts on Oocyte and Offspring.Antioxidants. 2020; 9: 95Crossref Scopus (9) Google Scholar), which may confound the observation (Figure 1C). Additionally, RNA-sequencing bias when dealing with highly modified RNAs such as tRNAs/tsRNAs remains an unmet challenge when quantitatively interpreting the sncRNA-seq data (Zhang et al., 2019Zhang Y. Shi J. Rassoulzadegan M. Tuorto F. Chen Q. Sperm RNA code programmes the metabolic health of offspring.Nat. Rev. Endocrinol. 2019; 15: 489-498Crossref PubMed Scopus (52) Google Scholar). Finally, the involvement of ROS in epigenetic inheritance is thought provoking, because in addition to unhealthy diets, other environmental exposures including cigarette smoking and toxicants (e.g., arsenite and endocrine disruptors) may all convergently generate ROS in the developing germ cells, and ROS may function as a nexus for transmitting parental environmental stressors to offspring by integrating multiple epigenetic mechanisms. Admittedly, how exactly the sperm histone marks and sncRNAs interact to convey mammalian epigenetic inheritance remains elusive, but the conserved mechanism suggested in both flies and mice here (Seong et al., 2011Seong K.H. Li D. Shimizu H. Nakamura R. Ishii S. Inheritance of stress-induced, ATF-2-dependent epigenetic change.Cell. 2011; 145: 1049-1061Abstract Full Text Full Text PDF PubMed Scopus (197) Google Scholar, Yoshida et al., 2020Yoshida K. Maekawa T. Ly N.H. Fujita S.I. Muratani M. Ando M. Katou Y. Araki H. Miura F. Shirahige K. et al.ATF7-Dependent Epigenetic Changes Are Required for the Intergenerational Effect of a Paternal Low-Protein Diet.Molecular Cell. 2020; 78 (this issue): 445-458Abstract Full Text Full Text PDF Scopus (11) Google Scholar) sheds a ray of light before the door finally opens for mammals, if open it will. ATF7-Dependent Epigenetic Changes Are Required for the Intergenerational Effect of a Paternal Low-Protein DietYoshida et al.Molecular CellMarch 19, 2020In BriefYoshida et al. report that ATF7 is a key mediator of paternal low-protein diet (LPD)-induced intergenerational inheritance. In the testis, LPD induces ATF7 activation via ROS, leading to H3K9me2 reduction on ATF7 target genes. This epigenetic change is maintained in spermatozoa and affects the pattern of small RNA expression. Full-Text PDF Open Archive
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