«We found dysregulated expression in a suspect
gene complex which adds to evidence that PMDD is a disorder of cellular response to estrogen and progesterone,» explained Peter Schmidt, M.D. of the NIH's National Institute of Mental Health, Behavioral Endocrinology Branch.
Not exact matches
That doesn't change the fact that an animal born with an abnormality
which makes it more
complex but also better suited to survive would live to pass on that
gene to it's children and slowly to the entire species.
The issue should be understood as «
which is more important, the individual replicator (the
gene), or the patterns generated by interactions of a myriad of replicators with a
complex environment?»
But it is not actually the crucial question,
which is, What controls the activity of the
complex interacting set of
genes,
which produces a nerve cell or a muscle cell?
These experiments were complemented by genetic manipulations in
which some mice were engineered to lack a
gene known as Tap1,
which is crucial for the MHC I
complex to make its way to the cell surface.
Individual body odor is influenced by
genes, and by one group in particular: the
genes that determine
which proteins combine to form your unique major histocompatibility
complex (MHC).
The study identifies a wide set of
genes — previously associated with
complex structures in higher animals —
which were supposedly absent in sponges.
They achieved this by transiently disturbing interactions between target
genes and PcG proteins,
which are
complexes involved in the repression of several
genes governing development.
If cells were infected with an influenza A mutant lacking NS1, they proceeded to produce large number of the molecular
complexes required for RNAi,
which include a protein called Argonaute that slices through the target
gene.
To make things more
complex, there's the epigenome — the chemical modifications to DNA that help control
which genes are turned on and off — and the transcriptome, the full range of RNAs that translate DNA's blueprints so they can be used to make proteins.
The process by
which bacteria make cellulose and secrete it to build biofilms is already quite
complex, regulated by more than a dozen different
genes working together.
The investigators also found
complex indels in a
gene called KIT,
which appears to play a role in melanoma.
In particular, the researchers identified
complex indels in the
gene EGFR,
which is implicated in lung cancer.
The analysis suggests that patients with
complex indels in KIT would benefit from drugs such as imatinib, sunitnib and sorafenib,
which target mutations in this
gene.
Women prefer the smell of T - shirts worn by men whose major histocompatability
complex genes —
which encode the proteins that make up an important part of our immune system — are different from their own, and vice versa.
Understanding this process -
which is particularly important when cells are first taking on specialized identities such as nerve cells, muscle, skin, and so on - helps explain how
complex organisms can arise from a finite number of
genes.
«First, there is no single road map to eusociality — the
complex, cooperative social system in
which animals behave more like superorganisms than individuals fending for themselves,» said
Gene Robinson, a lead on the study who is a professor of entomology and director of the Carl R. Woese Institute for Genomic Biology at the University of Illinois.
This essentially gives us «barcodes» of specific
gene loci,
which we can use to help untangle the
complex genetics of
complex diseases,» said Andrey Rzhetsky, PhD, professor of genetic medicine and human genetics at the University of Chicago, who led the study.
And even if such a demand existed, there was no evidence that genetic counseling could help patients with psychiatric disorders,
which — like most of the more common diseases — are caused by a
complex interplay of multiple
genes and variants as well as environmental factors.
She said: «Identifying a fault in
Complex I, one of the building blocks of mitochondria
which is responsible for causing disease combined with our custom
gene capture and the latest sequencing technology means we can screen many more
genes to diagnose this debilitating disease.
Our capacity for
complex speech might come from tiny fiddles to existing monkey
genes,
which gave us flatter faces and more refined larynxes
When the team looked at what
gene signatures the RORγt - dependent ILCs expressed, they found high expression of major histocompatibility
complex class II (MHCII) protein,
which some cells use to display foreign proteins to the immune system and directly interact with T cells.
In their quest to decipher the
complex code of autism,
which can run in families, most scientists have focused on
genes.
- Our results provide new insights into the mechanisms of how POLR3G
gene regulates stem cell state,
which in turn sheds light on the
complex mechanisms with
which human embryonic stem cells both self - renew and maintain the ability to differentiate.
«The parts of the human genome linked to
complex diseases such as heart disease, cancer and neurological disorders can often be far away from the
genes they regulate, so it can be dificult to figure out
which gene is being affected and ultimately causing the disease.»
For more than a decade, the husband - and - wife team has been investigating how a large protein
complex called SAGA,
which helps control
gene activity in organisms from yeast to humans, influences developmental processes.
Dana Kolpin of the US Geological Survey in Iowa City says that the findings highlight the
complex issue of antibiotic - resistance
genes,
which will continue to be of concern as treated effluent becomes more widely used in regions that have scarce water resources.
These
complexes lead to mutations in the TP53 tumor suppressor
gene,
which in turn initiate the process toward kidney cancer.
Humans, to be human, don't need to have evolved unique
genes that code for entirely novel types of neurons or neurotransmitters, or a more
complex hippocampus (with resulting improvements in memory), or a more
complex frontal cortex (from
which we gain the ability to postpone gratification).
Almost 200 people joined DoSER on December 13 for the 2012 Annual Holiday Lecture
which explored the
complex relationship between
genes and human identity.
«Crohn's disease is a
complex disorder with multiple
genes and environmental factors involved,
which disproportionally affects individuals of Ashkenazi Jewish ancestry,» explained lead researcher Inga Peter, Professor of Genetics and Genomic Sciences at the Icahn School of Medicine at Mount Sinai in New York City.
Some of the
genes control receptors called integrins,
which help cells attach to and communicate with one another, allowing formation of specialized organs and
complex body plans.
That
gene encodes a protein called BAF 180,
which is a subunit of the PBAF subtype of the SWI / SNF chromatin remodeling
complex.
BET proteins can have a huge impact on
gene activity because they belong to a class of molecules called epigenetic readers,
which recognize special marks on DNA - protein
complexes and attract
gene - activating proteins to those spots.
These
genes include PRMT5,
which codes for a key enzyme that ensures proper maturation of the spliceosomal
complex.
It is much longer and more
complex than most viral or bacterial
genes, and it has sequences with
which other spider
genes can interact.
An analysis of all
gene transcription in the cultured cell lines turned up a large
gene complex in
which gene expression differed conspicuously in cells from patients compared to controls.
Such disorders are caused by
complex interactions among
genes and environmental factors; the challenge facing researchers now is to find out
which genes are involved and how they influence disease.
One of the
gene's molecular targets, for example, is a microRNA (a small noncoding RNA molecule) called let7,
which in turn regulates hundreds of other
genes, so the effects of Lin28a can set off a
complex array of regulatory interactions.
The reasons for this failing range from insufficient information from
which to predict system behavior to the inability of a
complex biologic system to be reductively explicable by the basal elements (
genes, proteins) from
which it emerges (Kim, 2006)(vide infra).
«The ways in
which particular
genes influence cancer risk are highly
complex.
This narrow view has been becoming overshadowed by genetic findings that support the more recent hypothesis of
complex roots,
which emphasizes lateral genetic exchanges or horizontal
gene transfers (HGT) rather than vertical mutational progression in the development of nucleated organisms, through a clearly defined «tree of life» (Mark Buchanan, New Scientist, January 26, 2010).
Although
gene regulation is
complex and we still have a lot to learn, scientists do know of three ways in
which our
genes are turned off and on.
The
complex then migrates into the cell nucleus, and activates the transcription of specific target
genes which are involved in physiological and pathological bone formation (Chen, Deng & Li, 2012; Katagiri & Tsukamoto, 2013; Miyazawa et al., 2002).
Diana Hargreaves studies a particular epigenetic regulator, the SWI / SNF
complex,
which uses energy to unpack and unwind DNA from structural proteins to alter DNA accessibility and in turn,
gene transcription.
The process by
which yeast form spores involves many more
genes and is more
complex than researchers had expected, according to studies by scientists at the University of California, San Francisco -LRB-...
Further, his group pioneered expression quantitative trait locus (eQTL) studies,
which enabled variation in global
gene expression to be applied to genetics of
complex human diseases.
The data is manually curated,
which is more accurate at identifying splice variants, pseudogenes poly (A) features, non-coding and
complex gene structures and arrangements than current automated methods.
Two clock proteins, CLOCK (Circadian locomoter output cycles protein kaput) and BMAL1 (Brain and Muscle Arnt - like1) bind to each other to form a heterodimer
complex,
which then binds to a DNA sequence called E-box (CACGTG) located in the upper region of clock
genes, Per (Period) and Cry (Cryptochrome), present in the genome.
Activated E2F leading to transcription of several target
genes including cyclin E in late G1 phase
which form active
complex with CDK2 drives progression from G1 to S phase [7].