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Genetics Part I
Genetics Part I

... We will begin by looking at a special kind of cell division called meiosis. Meiosis is from the Greek word for "diminution," which means to make smaller. This is the process that results in egg and sperm cells with one half of the normal number of chromosomes. Egg and sperm unite to form a new indiv ...
Chapter 10: DIPLOIDY
Chapter 10: DIPLOIDY

... In 1992, R.E. Smith & D.E. Goldberg extended their research and examined the effects of diploid representations and dominance operators in genetic algorithms applied to nonstationary search problems. Analytical and experimental evidence showed that a diploid GA maintained extra diversity at loci whe ...
Mendelian inheritance
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... Biology  Underlying  Mendel’s  Laws Cell  Division   Mitosis:    Used  for  growth  and  replacement  of  worn  out  cells.    Creates  new  cells   genetically  identical  to  old  ones.   Meiosis:    Used  for  reproduction.  Creates   ...
DETERMINING THE BEST MUTATION PROBABILITIES OF A
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Y chromosome: Structure and Biological Functions
Y chromosome: Structure and Biological Functions

... and heterochromatic sequences. The heterochromatic region is assumed to be genetically inert and polymorphic in length in different male populations, because it is composed mainly of two highly Fig1: Human Y chromosome ...
Beads on a string Bowater Biochem Soc Trans 2012
Beads on a string Bowater Biochem Soc Trans 2012

... flux along the DNA, and one type of machine that modulates this dynamic behaviour are the remodelling factors. Tim Richmond [8] described the structure of the yeast ISW1 (imitation switch chromatin remodelling 1) chromatin remodelling factor and provided structural data for the interaction of ISW1 o ...
Blueprint for life - Siemens Science Day
Blueprint for life - Siemens Science Day

... Inside the nucleus, draw a simple sketch of DNA as two straight strands with connecting “rungs” like a ladder. Explain that the DNA represents a code for molecules called proteins, much like the series of numbers represents a code for the word hello. Draw an arrow from the DNA to the cytoplasm porti ...
Inquiry into Life Twelfth Edition
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... – DNA winds almost twice around the histone core condensing DNA length by 6- to 7-X – Core histones contain a histone fold: • 3 a-helices linked by 2 loops • Extended tail of about 28% of core histone mass ...
Class 5: Biology and behavior
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... Methods of detection are available for those who are high risk. Ultrasound: high-frequency sound waves give picture of fetus – gross physical defect can be seen. Amniocentesis; most common: needle inserted to abdominal wall. Uterus fluid is obtained. Cells examined. • But, can cause miscarriages or ...
doc THREE finals
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... • Highly condensed, heterochromatinized • Euchromatin – relaxed, open – transcriptionally active • Heterochromatin – compact, condensed – poor access by transcription factors • Highly methylated ...
Chapter 11 notes
Chapter 11 notes

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unit v – mendelian genetics
unit v – mendelian genetics

... • X Inactivation in Females o During embryonic development, one X chromosome in female cells is inactivated due to addition of methyl group to its DNA o Dosage compensation o Inactive X chromosome condenses; known as Barr body o Occurs randomly  Females will have some cells where “Dad’s copy” of X ...
Example 2 – Human Skin colour
Example 2 – Human Skin colour

... Autosomes are chromosomes, which are not sex chromosomes. They are the other 22 pairs, for example, in humans. Sex chromosomes are those chromosomes, which help in determining the sex of an individual (XX or XY). In our studies, we have studied that genes independently assort. In other words, they a ...
IVRI OB 1809
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... its old character reappears. We therefore say that there must be material particles within the organism which reproduce themselves without change and determine this constancy within il. That at least was the simplest assumption and one that was made long before any such particles were seen. The corp ...
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...  Autosomal dominant inheritance  Disorder manifest in both homo and heterozygote  Both sexes can be affected but their can be ...
PDF version - Atlas of Genetics and Cytogenetics in Oncology and
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... an anaphase bridge, followed by chromosome breakage, subsequent fusion of damaged ends, and promotion of additional BFB cycles VI.3.4. Recurring cycles of gene amplification can arise during acquisition of new telomeres by rearranged chromosomes, suggesting double-stranded DNA breaks are important i ...
The Cytogenetic Basis of Human Infertility: A Review Bheem Prasad
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... karyotype 47, XXY, which can be in all cells or in mosaic form. There are various extents of spermatogenetic failure, but males are generally sterile3,11,12. The gonadal defect in XXY male seems to be related to germ cell survival and sex chromosome constitution. It is through that the testicular at ...
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X-Chromosome Inactivation: The Case of the Calico Cat1
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... This is a cat with the coat color commonly referred to as calico. (A colored overhead, slide, or best of all, a living, purring cat in the classroom, is shown at this point.) Those of you who have had such a cat know one crucial fact about them; they must be spayed, or you will end up with lots of p ...
Mutations - Warren County Schools
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... deleterious, or lethal. For example, induction of frameshift mutation has been used to make certain bacteria capable of producing nylonase, an enzyme that can degrade nylon. • Frameshift mutation has also been one of the possible causes of albinism. A shift in the reading frame can lead to formation ...
Bacteria are important “nitrogen fixers” Bacteria and fungi are
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...  Microorganisms are any small organism – too small to see with the naked eye include  Pathogens – cause disease  Most bacteria are not pathogens ...
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... attachment at the kinetochore, the mitotic checkpoint genes regulate the cell cycle to ensure accurate chromosome alignment and segregation at anaphase to generate euploid daughter cells. Loss of appropriate chromosome attachments at the kinetochore or defects in the mitotic spindle lead to cell cyc ...
Chromatin Structure Is a Focus for Regulation 30.2
Chromatin Structure Is a Focus for Regulation 30.2

... Two broad classes of chromatin: – Euchromatin: Majority chromatin is in its extended (decondensed) state during interphase, only condenses during mitosis. – Heterochromatin: Remains highly condensed even in interphase. Accounts for the dark staining regions seen in interphase chromatin. Heterochroma ...
Mendel Discovers “Genes” 9-1
Mendel Discovers “Genes” 9-1

... Mendel ____________________ making parts and ____________ added pollen from _______ another plant. This allowed him to _____________ cross-breed plants with ______________ different characteristics and study the results ________ ...
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Chromosome



A chromosome (chromo- + -some) is a packaged and organized structure containing most of the DNA of a living organism. It is not usually found on its own, but rather is complexed with many structural proteins called histones as well as associated transcription (copying of genetic sequences) factors and several other macromolecules. Two ""sister"" chromatids (half a chromosome) join together at a protein junction called a centromere. Chromosomes are normally visible under a light microscope only when the cell is undergoing mitosis. Even then, the full chromosome containing both joined sister chromatids becomes visible only during a sequence of mitosis known as metaphase (when chromosomes align together, attached to the mitotic spindle and prepare to divide). This DNA and its associated proteins and macromolecules is collectively known as chromatin, which is further packaged along with its associated molecules into a discrete structure called a nucleosome. Chromatin is present in most cells, with a few exceptions - erythrocytes for example. Occurring only in the nucleus of eukaryotic cells, chromatin composes the vast majority of all DNA, except for a small amount inherited maternally which is found in mitochondria. In prokaryotic cells, chromatin occurs free-floating in cytoplasm, as these cells lack organelles and a defined nucleus. The main information-carrying macromolecule is a single piece of coiled double-stranded DNA, containing many genes, regulatory elements and other noncoding DNA. The DNA-bound macromolecules are proteins, which serve to package the DNA and control its functions. Chromosomes vary widely between different organisms. Some species such as certain bacteria also contain plasmids or other extrachromosomal DNA. These are circular structures in the cytoplasm which contain cellular DNA and play a role in horizontal gene transfer.Compaction of the duplicated chromosomes during cell division (mitosis or meiosis) results either in a four-arm structure (pictured to the right) if the centromere is located in the middle of the chromosome or a two-arm structure if the centromere is located near one of the ends. Chromosomal recombination during meiosis and subsequent sexual reproduction plays a vital role in genetic diversity. If these structures are manipulated incorrectly, through processes known as chromosomal instability and translocation, the cell may undergo mitotic catastrophe and die, or it may unexpectedly evade apoptosis leading to the progression of cancer.In prokaryotes (see nucleoids) and viruses, the DNA is often densely packed and organized. In the case of archaea by homologs to eukaryotic histones, in the case of bacteria by histone-like proteins. Small circular genomes called plasmids are often found in bacteria and also in mitochondria and chloroplasts, reflecting their bacterial origins.
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