«Germline editing» — genetic
modification of human cells, including embryos, eggs and sperm, that can be passed to future generations — has been controversial.
Not exact matches
Therefore, it is essential that we learn how specific types
of chemical
modifications normally regulate RNA function in our
cells, in order to understand how dysregulation
of this process contributes to
human disease, says Cristian Bellodi.
Since pseudouridine
modifications may affect various RNA molecules in different types
of normal and malignant
cells, «our discoveries pave the way for future avenues
of research aimed at exploring the role
of pseudouridine in
human development disease,» concludes Cristian Bellodi.
Dr. Bellodi's laboratory uncovered a new important function
of pseudouridine, the most common type
of RNA
modification in
human cells.
Researchers in optogenetics can control genetically modified brain
cells using light but because
of these
modifications, the technique is not yet deemed safe to use in
humans.
The researchers have shown that it is possible to produce chromosome
modifications in
human cells that are genetically identical to those observed in leukemia and other types
of human cancer.
In the
human body
cells turn genes on and off by means
of chemical
modifications that change DNA and related proteins.
That paper, which tried to correct a mutation that causes a blood disease, fed into a firestorm over the ethics
of modifying
human reproductive
cells (or «germline»
modification).
In the Nature papers, the researchers compared gene transcription, chromatin
modification and other processes that control gene activity in a wide range
of mouse and
human tissues and
cell types.
«While genetic
modification of crops can introduce new beneficial traits into existing crops, the resulting products need to be tested for long - term health effects before making assumptions about their impact on
human health,» said senior investigator Frances Sladek, a professor
of cell biology and neuroscience at UC Riverside.
Marson stressed that, while recent reports
of CRISPR / Cas9 editing
of human embryos have stirred up controversy, T
cells are created anew in each individual, so
modifications would not be passed on to future generations.
The NIH Roadmap Epigenomics Consortium has just published the largest collection
of epigenomes characterized to date: 111 primary
human tissues and
cells profiled for histone
modification patterns, DNA accessibility, DNA methylation, and gene expression.
One
of my favorite papers from this year was the landmark publication
of the NIH Epigenomics Roadmap Consortium, which profiled 111 primary
human tissues and
cell types for histone
modification patterns, DNA accessibility, DNA methylation, and gene expression.
Now, in Stem
Cells Translation Medicine, the group
of Shu Wang at the National University
of Singapore describe the derivation
of EPCs from
human iPSCs, their therapeutic
modification, and their ability to inhibit tumor growth in a mouse breast cancer model [4].
Modification of human embryonic stem
cell - derived dendritic
cells with mRNA for efficient antigen presentation and enhanced potency.
The molecules central to this balancing act, H3K4me3 and H3K27me3, are among the so - called epigenetic
modifications that influence the activity patterns
of genes in both
human embryonic stem (ES)
cells and mature
human adult
cells.
A
human embryonic stem
cell is reined in — prevented from giving up its unique characteristics
of self - renewal and pluripotency — by the presence
of a protein
modification that stifles any genes that would prematurely instruct the
cell to develop into heart or other specialized tissue.
While many important developments impacted the field, two that garnered significant public, political and scientific attention in 2016 were the proliferation
of clinics using unproven stem
cell «therapies,» and the steps forward in therapeutic
modification of human oocytes (unfertilized eggs) through a process called mitochondrial replacement therapy (MRT).
Dr. Vijayanand also oversees a large - scale effort to map epigenomic
modifications in more than a dozen different types
of human immune
cells from normal individuals to understand how epigenetic variations cause susceptibility to disease.
Publication in Molecular
Cell on reversal
of base
modifications in messenger RNA (mRNA) and role in
human disease
The quality and novelty
of the data, leads to new insights into the replication landscape
of the
human genome and to further unravel the links between replication, gene expression, epigenetic
modification and 3D genome organization in normal and cancer
cells.
Vijay also oversees a large - scale effort to map epigenomic
modifications in more than a dozen different types
of human immune
cells from normal individuals to understand how epigenetic variations cause susceptibility to disease.
«Before our technique, genetic
modification of human embryonic stem
cells largely was inefficient,» Hohenstein said.
[PRESS RELEASE 2017-05-05] A new study in Science from Karolinska Institutet maps out how different DNA - binding proteins in
human cells react to certain biochemical
modifications of the DNA molecule.
Dissertation: «Epigenetic
Modification of Vitamin D - induced Gene Expression in
Human Colorectal and Breast Cancer
Cell Lines.»
Keiichiro Suzuki, a CRISPR expert from Salk Institute researcher, also not involved in the study, said by email: «Due to the high stability, specificity and ease for biosynthesis, the synthetic CRISPR RNA approach developed in this study will facilitate targeted genetic
modification in a variety
of human cells for fundamental studies as well as therapeutic applications»
Epidemiological evidence and intervention studies clearly show that in
humans saturated fat significantly worsen insulin - resistance, while monounsaturated and polyunsaturated fatty acids improve it through
modifications in the composition
of cell membranes which reflect at least in part dietary fat composition.
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