Quantification of Histone Acetyltransferase and Histone Deacetylase Transcripts

Mammalian oocytes are very unique cells with an unlimited developmental potential. These totipotent cells are able to remove existing gene-expression patterns and to impose new ones.

However, genome reprogramming is still a mystery. Posttranslational modifications by acetylation of the N-termini portion of histones composing the nucleosome are involved in genome reprogramming. These modifications alter the higher-order chromatin structure to render the DNA accessible to the regulatory and transcriptional machinery.

In the present study, we have investigated, to our knowledge for the first time, precise expression patterns of seven genes involved in chromatin structure throughout bovine embryo development. Oocytes harvested from bovine ovaries were used for in vitro production of germinal vesicle oocytes, metaphase II oocytes, 2- and 8-cell embryos, and blastocysts. Total RNA was extracted from pools (triplicates) of 20 oocytes or from embryos of each developmental stage. By means of quantitative reverse transcription-polymerase chain reaction using SYBR Green to detect double-stranded DNA, mRNA expression profiles for histone deacetylases (HDAC1, HDAC2, HDAC3, and HDAC7), histone acetyltransferases (GCN5 and HAT1), and histone H2A were established.

Transcripts for all genes were detected at all stages from the oocyte to the blastocyst. The HDAC1, HDAC2 (class I HDAC), and HAT1 (type B HAT) revealed similar expression profiles. The HDAC3 (class I HDAC) tends to have an expression profile similar to those of HDAC1, HDAC2, and HAT1, whereas the HDAC7 (class II HDAC) and GCN5 (type A HAT) profiles were different from those three. These results indicate variable levels of histone deacetylases and histone acetyltransferases throughout embryonic development and may indicate the ones that are involved in somatic remodeling.

On the Nature and Origin of DNA Strand Breaks in Elongating Spermatids

Transient DNA strand breaks are generated in the whole population of elongating spermatids and are perfectly coincident with histone H4 hyperacetylation at chromatin-remodeling steps. Given the limited DNA repair capacity of elongating spermatids, chromatin remodeling may present a threat to genetic integrity of the male gamete. The nature of the DNA strand breakage, the enzymes involved, and the role of H4 hyperacetylation in the process must be determined to further investigate the potential mutagenic consequences of this important transition. We used the metachromatic dye acridine orange in combination with fluorescence-activated cell sorting to achieve separation of spermatids according to their condensation state. Using single-cell electrophoresis (comet assay), in both alkaline and neutral conditions, we demonstrated that double-stranded breaks account for most of the DNA fragmentation observed in purified elongating spermatids. DNA strand breaks were generated in round spermatids as a result of de novo histone hyperacetylation induced by trichostatin A, whereas an increase in endogenous DNA strand breaks was observed in elongating spermatids. Using a short-term culture of testicular cells, we demonstrated that DNA strand breaks in spermatids were abolished on incubation with two functionally different topoisomerase II inhibitors. Hence, topoisomerase II appears as the unique enzyme responsible for the transient double-stranded breaks in elongating spermatids but depends on histone hyperacetylation for its activity.

Regulation of supply and demand for maternal nutrients in mammals by imprinted genes

The placenta has evolved in eutherian mammals primarily to provide nutrients for the developing fetus. The genetic control of the regulation of supply and demand for maternal nutrients is not understood. In this review we argue that imprinted genes have central roles in controlling both the fetal demand for, and the placental supply of, maternal nutrients. Recent studies on Igf2 (insulin like growth factor 2) knockout mouse models provide experimental support for this hypothesis.

These show effects on placental transport capacity consistent with a role of IGF-II in modulating both the placental supply and fetal demand for nutrients. Imprinting of genes with such functions may have coevolved with the placenta and new evidence suggests that transporter proteins, as well as the regulators themselves, may also be imprinted. These data and hypotheses are important, as deregulation of supply and demand affects fetal growth and has long term consequences for health in mammals both in the neonatal period and, as a result of fetal programming, in adulthood.

Insulator Mechanism of Imprinting : (e.g. H19 & IGF2 genes)

The H19 and IGF2 genes, the essential regulatory elements coordinating their imprinted expression have been well characterized. Shared enhancers that regulate H19 and IGF2 in endodermal and mesodermal tissues have been delimited. An imprinting control region (ICR) has been well defined and consists of a CG-rich differentially methylated domain (DMD), located 22 to 24 kb relative to the H19 transcription start site. The human H19 DMD encompasses seven different binding sites for CTCF. Only the sixth CTCF binding site has been reported to act as a key regulatory domain for switching between H19 and IGF2 expression, whereas the other sites appear to be hypermethylated in a study by Takai et al.

This DMD is essential for establishing the pattern of imprinting by which H19, a non-coding RNA, is exclusively expressed from the maternal chromosome and IGF2, a fetal growth factor, is only active paternally.

DMD has at least two distinct regulatory roles on each of the parental chromosomes. The activity of the DMD is determined by its methylation status. On the maternal chromosome, the DMD is hypomethylated and binds the protein CTCF via four highly conserved CG-rich repetitive sites. The binding of CTCF creates a physical boundary on the maternal allele and inhibits interaction of downstream enhancers with IGF2 promoters.

Maternal binding of CTCF to the four sites within the DMD has been further hypothesized to protect actively the region from becoming methylated during oogenesis and development. The DMD is also essential for optimal H19 and IGF2 expression and is required on the maternal allele for the initiation of H19 expression. On the other hand, the paternal H19 DMD is hypermethylated and hence the CTCF is unable to bind to it, resulting in expression of IGF2 while H19 is silenced.

DNA Methylation & Gene Expression

In mammals DNA methylation occurs after DNA replication and involves the transfer of a methyl group from S-adenosyl-methionine (SAM) to the 5’ – position of cytosine residues, in a reaction catalysed by the enzyme DNA methyltransferase (Dnmt). Three enzyme families associated with DNA, identified are as follows :

DNA methyltransferase I   : primarily mediates maintenance of methyl    transferase  activity during the  S phase.

DNA methyltransferase II       :  plays a role in some aspects of  centromere function.

DNA methyltransferase III           :    plays an essential role in the de novo

[ Dnmt3a and Dnmt3b ]                    methylation in vivo.

DNA Methylation & Gene Expression :

CpG island is usually the site for DNA methylation. CpG islands are genomic regions that contain a high frequency of CG nucleotides. They are regions with at least 200 bp and with a GC percentage that is greater than 50% and with an observed/expected CpG ratio that is greater than 60%. CpG islands typically occur at or near the transcription start site of genes, particularly housekeeping genes. They act as strong promoters and have also been proposed to function as replication origins. It is estimated that CpG islands are associated with about half of all mammalian genes. Unmethylated CpG islands are associated house keeping genes, while the CpG islands of many tissue-specific genes are methylated, except in the tissues where they are expressed. Interactions between proteins and DNA are changed by methylation, leading to alterations in chromatin structure and a transcription rate change. Thus DNA methylation mechanisms for gene regulation can be as follows :

·         Preventing the binding of transcription factors to their target sequences via proteins that bind preferentially to methylated promoters.

·         Interfering with the binding of transcription factors to the methylated cytosine.

·         Altering the chromatin structure leading to a change in the rate of transcription.

The best-characterized cluster that follows a strict insulator model for imprinted expression is the cluster containing maternally expressed H19 and paternally expressed insulin-like growth factor 2 (IGF2). This cluster resides at 11p15.5 in humans and is found in conserved synteny on distal chromosome 7 in mice.

Human chromosome 11p15.5 contains a large cluster of imprinted genes spanning a region of 1-Mb. This cluster can be divided into two independent imprinting sub-domains: one containing H19, IGF2 and INS2 (H19 domain) and other containing CDKN1C, KCNQ1, ASCL2 and TSSC3 (KCNQ1 domain). These two domains contain several genes that play a role in embryo growth. Regulatory disturbances of a number of genes in this cluster result in imprinting disorder like Beckwith-Wiedemann Syndrome (BWS), Silver Russell Syndrome (SRS) and increased predisposition to development of specific embryonic tumors, like Wilm’s Tumor (Verona et al., 2003).

While most studies on H19 and IGF2 have been performed in the mouse, many attributes of these genes including their expression profile and regulatory mechanisms are similar in humans. In both mouse and human, H19 and IGF2 are widely expressed during embryonic development and postnatally down regulated in most tissues.

H19 encodes a fully processed 2.3 kb non-coding RNA and was initially implicated as a tumor suppressor. However, it has also been shown to have oncogenic properties. IGF2 encodes a protein that plays a major role in promoting embryonic and placental growth and development.

As with all imprinted clusters, imprinted expression of H19 and IGF2 is regulated by Imprinting Control Region [designated imprinting center 1 (IC1) in humans and ICR or differentially methylated domain (DMD) in mouse] located between the two genes. This region is approximately 5 kb and 2 kb long in humans and mice, respectively.

The H19 and IGF2 genes are co-coordinately regulated, most probably through interaction of either promoter with a common ‘enhancer element’ and the action of a further insulator.

Insulator proteins, such as CTCF (a zinc finger CCCTC-binding factor) and BORIS have been demonstrated to bind to specific DNA elements and prevent promoter and enhancer interaction. CTCF is present in both somatic and germ cells, whereas BORIS is expressed specifically in the male germ line and has been suggested to be associated with both demethylases mediating erasure of imprinting marks and methylases mediating de novo methylation.

Epigenetic Regulation of Imprinting

Imprinting is regulated by the interplay of different epigenetic components which are as follows :


• DNA methylation.
• Chromatin structure.
• Degree of histone acetylation.


Among all these, one of the key factors that play a major role in the epigenetic modification of the genome is DNA methylation.

Life Cycle of an Imprint

Life cycle of an imprint is a dynamic process, which involves erasure, establishment, maintenance and implementation of the imprint markings.


Erasure and Establishment :


Each gamete carries sex specific imprint markings that are required for normal development. Upon fertilization, the paternal pronucleus is rapidly and actively demethylated within the zygote prior to first cellular division. In contrast, the maternal genome becomes demethylated in a passive manner during subsequent divisions, presumably due to lack of Dnmt – 1.

Erasure of the paternal methylation profile by the oocyte is a potentially powerful mechanism by which maternal factors modify chromatin structure to regulate the paternal genome. Demethylation at this stage is proposed to be required for the activation of genes necessary for the early embryonic growth. However imprint methylation marks present on both the paternal and maternal genomes are maintained despite this global demethylation event.


Another reprogramming event occurs later, within the primordial germ cells of the developing fetus. After the demethylation in the primordial germ cells, parental specific methylation is re-established during gametogenesis. This occurs in sperm post-natally within diploid genocytes prior to meiosis and within oocytes arrested at the diplotene stage of meiosis.


In the oocyte, the Dnmt 3 family of methyltransferases is required to set maternal specific methylation patterns for imprinted genes. Dnmt 3a and Dnmt 3b play an important role in establishing methylation patterns in oocytes.