Download - Chromosomes and Chromatin
CHROMOSOMES AND CHROMATIN
Juan Nicolás Sarmiento Naranjo Medicine Student
Pontifical Bolivariana University||| Semester
CHROMOSOMES AND CHROMATIN
MADE BY: JUAN NICOLÁS SARMIENTO NARANJO
MOLECULAR BIOLOGY
||| SEMESTER
TEACHER: LINA MARTINEZ
BIBLIOGRAPHY
• Researchers discover mechanism of gene silencing in hormone-dependent breast cancer cells. (2016, July 8) http://www.news-medical.net/news/20160708/Researchers-discover-mechanism-of-gene-silencing-in-hormone-dependent-breast-cancer-cells.aspx
• Scientists discover X-chromosome-inherited type of osteogenesis imperfecta (2016, July 6) http://www.news-medical.net/news/20160706/Scientists-discover-X-chromosome-inherited-type-of-osteogenesis-imperfecta.aspx
MEDICAL UTILITY This both news revealed how science and all the medical stuff are applying the tecnology to find new techniques and processes on the genetic material to treat some pathologies that are involved the DNA in any form of packing: chromosomes or chromatin.
The possibility to have a mistake in some part of the DNA is very big and cause many dissease, like Cancer or Osteogenesis imperfecta. The first one is one of the most prevalent in all the world and is guilty of the death of many people. And the second one, (O.I) doesn´t have the same concurrence of CA but symptoms are very serious.
INTRODUCTION
The DNA in eukaryotic cells is a double helix that is organized in a specific way , which presents a packing process with some proteins and resulting a condensation called chromatin, and subsequently condensed in chromosomes to perform the division. In the cell cycle, the chromosomes has a very important job because they´re the performer of the equal division of genetic material.
Scientists discover X-chromosome-inherited type of osteogenesis imperfecta
Some researchers from the Zurich´s Hospital have found that the X chromosome is involved in the congenital disease of Osteogenesis imperfecta. Is a new tipe of brittle- bone disease who is caused for two mutations
of the gen MBTPS2 in the X chromosm. This makes men (caryotip XY) more vulnerable.
STUDENT´S OPINION: I think this discovery is very important because all the medical staff can be more forwarned of the treatments and previous diagnosis of the osteogenesis imperfecta, avoiding the increase of the patients.
Researchers discover mechanism of gene silencing in
hormone-dependent breast cancer cells
Cancer cells have been studied for many years, and now, some researches have found a protein that can interact repressing the progesterone receptor, and compacting the chromatin, making them very difficult to continue its process correctly, and intervene inthe proliferation or death of the breast cancer cells, avoiding some kind of neoplasia.
STUDENT´S OPINION: Today, the breast cancer has elevated its presence in women, affecting them and now with the progress of the science, reprresing that cells is a very good step not only for the medicine but also for the people´s health
INTRODUCTION
The DNA has a packing procces with a condensation
Double helix, nucleosome, chromatosome, solenoid ( 30 nm long), and chromosome.
A fundamental characteristic of cells is their hability to divided.
The cell cycle is based in four steps: Prophase, Metaphase, Anaphase and Telophase, with finally the cytokinesis.
SCIENTISTS DISCOVER X-CHROMOSOME-INHERITED TYPE OF OSTEOGENESIS IMPERFECTA
UNIVERSITY OF ZURICH
(2016, JULY 6)
SCIENTISTS DISCOVER X-CHROMOSOME-INHERITED TYPE OF OSTEOGENESIS IMPERFECTA
Osteogenesis imperfecta is one of the most brittle-
bone congenital dissease that affects children in all
around the world.
The patients have symptoms like bone fragility,
deformities and stunted growth.
SCIENTISTS DISCOVER X-CHROMOSOME-INHERITED TYPE OF OSTEOGENESIS IMPERFECTA
The osteogenesis imperfecta is caused by two mutations of the same gen (MBTPS2) in the x chromosome, that encodes a protease involved on the bone formation.
The prevalence of the X chromosome makes men more vulnerable to present this disease, and makes the woman the agent that can pass the DNA with the codificated information
SCIENTISTS DISCOVER X-CHROMOSOME-INHERITED TYPE OF OSTEOGENESIS IMPERFECTA
One gen is a part of the material genetic that its expression is very important to the
develop of any sickness. The gen MBTPS2 of the X chromosome is one of the cause of the O.I but also of dermatological disease, and maybe it can be the guilty of many illnes but now, the science can´t show us all the intervetion of the gens in all
kind of phenotypes.
STUDENT´S OPINION: I think this discovery is very important because
all the medical staff can be more forwarned of the treatments and
previous diagnosis of the osteogenesis imperfecta, avoiding
the increase of the patients.
SCIENTISTS DISCOVER X-CHROMOSOME-INHERITED TYPE OF OSTEOGENESIS IMPERFECTA
RESEARCHERS DISCOVER MECHANISM OF GENE SILENCING IN
HORMONE-DEPENDENT BREAST CANCER CELLS
RESEARCHERS DISCOVER MECHANISM OF GENE SILENCING IN HORMONE-DEPENDENT BREAST CANCER CELLS
The breast cancer is a neoplasia wich mainly affects women and in
low proportion men in the actuallity, with a differential sign that is a tumor in any part of the
breast.
RESEARCHERS DISCOVER MECHANISM OF GENE SILENCING IN HORMONE-DEPENDENT BREAST CANCER CELLS
Hormones are a substance that is excreteated by endocrine glands
and are related with the cell metabolism. There are many kinds of hormones, one of this are the
steroid hormones that are involved in the activity of the gens´s
expression. Progesterone is one of the hormones that the reaserchers study to inhibited their receptors
and SILENCE GENS
To repress a hormonal receptor they need a Complex of proteins wich are
FOX A1 and BRG1 that make a change on the chromosome estructure
generating a condensation of the genetic material and avoiding its
separtion to read all the information.
RESEARCHERS DISCOVER MECHANISM OF GENE SILENCING IN HORMONE-DEPENDENT BREAST CANCER CELLS
FOX A1
BRG1
Some gens are relacionated in death or proliferation cell, it depends of the complex that they are joined
STUDENT´S OPINION: Today, the breast cancer has elevated its presence in women, affecting them and now with the progress of the science, reprresing that cells is a very good step not only for the medicine but also for the people´s health
RESEARCHERS DISCOVER MECHANISM OF GENE SILENCING IN HORMONE-DEPENDENT BREAST CANCER CELLS
MEDICAL UTILITY
MEDICAL UTILITY
DNA studies and investigations has allowed in the present been reached of any specific part of the genetic material related to fenotipic expression in all the people. This has been a very big progress of the science, medicine and molecular biology. Scientists of past centuries proposed theories and techniques that now with all the technology we can do more easly.
MEDICAL UTILITY
PCR is one of the process that is used to obtain a clone of genetic material and get an amplification of
some especific part of the DNA to view some mistake or some special secuency.
Some techniques used in DNA process are
Human Genome Project is a research with the objective to show all the sequences of the DNA and
later make the process more convenient.
MEDICAL UTILITY
Cancer and Osteogenesis imperfecta are diseases with a bad forecast for the patient, and find a cure for this
illness is very hard because the science can´t get finally it. But, get a
treatment for the symptoms that pacients suffer is not only a step more in the science, but also is a
step to be more close of the end of the disease.
BIBLIOGRAPHY
• Researchers discover mechanism of gene silencing in hormone-dependent breast cancer cells. (2016, July 8) http://www.news-medical.net/news/20160708/Researchers-discover-mechanism-of-gene-silencing-in-hormone-dependent-breast-cancer-cells.aspx
• Scientists discover X-chromosome-inherited type of osteogenesis imperfecta (2016, July 6) http://www.news-medical.net/news/20160706/Scientists-discover-X-chromosome-inherited-type-of-osteogenesis-imperfecta.aspx
THE ART OF MEDICINE CONSISTS IN AMUSING THE PATIENT WHILE NATURE CURES THE DISEASE
-VOLTAIRE