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Prokaryotes - Nicholls State University
Prokaryotes - Nicholls State University

... extreme conditions that were likely common early in Earth’s history. ...
Chapter 12 Review2012 KEY
Chapter 12 Review2012 KEY

... No, the scientist could take a sample from a population and use the Hardy-Weinburg theory. A set of fraternal twins separated at birth and reared in different environments was studied to determine to what extent environmental factors shape development. What problem do you see in the reliability of s ...
Human Biology
Human Biology

... - The structure of DNA is called a “double helix” - The DNA contains instructions on how the cell should work - Genes control the development of characteristics (“it’s in the genes”) by issuing instructions to the cell to produce certain proteins - These proteins are either structural (used for cell ...
GA 1
GA 1

... A chromosome consist of genes, blocks of DNA. Each gene encodes a particular protein. Basically can be said, that each gene encodes a trait, for example color of eyes. Possible settings for a trait (e.g. blue, brown) are called alleles. Each gene has its own position in the chromosome. This position ...
Chapter 11 Notes
Chapter 11 Notes

...  At the end one diploid cell will become four haploid cells  Meiosis only occurs in reproductive cells ...
Lesson Overview - Enfield High School
Lesson Overview - Enfield High School

... Process in which the number of chromosomes per cell is cut in half through the separation of homologous chromosomes in a diploid cell One diploid cell goes through two separate divisions, producing four haploid cells ...
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... Growth in non-permissive host E. coli K12(); rare r+ recombinants grow (rare because the mutations are close to each other and crossover is infrequent). ...
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Genetics of bacteria and bacteriophages

... Growth in non-permissive host E. coli K12(); rare r+ recombinants grow (rare because the mutations are close to each other and crossover is infrequent). ...
The relation of genetics to physiology and medicine
The relation of genetics to physiology and medicine

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X-linked Genes

... People with red-green color blindness see either a three or nothing at all. ...
The relation of genetics to physiology and medicine
The relation of genetics to physiology and medicine

... order in the chromosomes is deducible, both from genetic evidence and from cytological observations. Whether the relative position is no more than a historical accident, or whether it is due to some relation between each gene and its neighbors, can not be definitely stated. But the evidence from the ...
Homologous Pairs- Pairs of chromosomes with the same genes on
Homologous Pairs- Pairs of chromosomes with the same genes on

... • Alleles on the same chromosome are often inherited together. • The closer the genes are to each other on a chromosome the more likely they are to be inherited together. • Alleles that are far apart can be separated by crossing over. ...
03 Non-mendelian Inheritance
03 Non-mendelian Inheritance

Idaho State University
Idaho State University

Genetics
Genetics

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Reproduction—The Importance of Reproduction
Reproduction—The Importance of Reproduction

... Sex Cells and Reproduction ...
Bacteria - REMC 8 / Kent ISD Moodle VLE
Bacteria - REMC 8 / Kent ISD Moodle VLE

...  •Bacteria DO have ribosomes, although the ribosomes are different in structure than eukaryotic ribosomes.  •Bacterial ribosomes are smaller than eukaryotic ribosomes, and have different protein and rRNA.  •However, archae have rRNA that is more similar in structure to eukaryotes than eubacteria ...
Barth Genetics
Barth Genetics

... Why can girls be carriers of Barth Syndrome? - As girls have two X chromosomes they will have two copies of the TAZ gene. So it is possible for a girl to have a spelling mistake in one copy of her TAZ gene which stops that copy of the gene working properly, but provided that the other copy of TAZ is ...
Basic genetics: Directed-study File
Basic genetics: Directed-study File

... FOXP2 is a protein that in humans is encoded by the FOXP2 gene, which is located on human chromosome 7. In humans, mutations of FOXP2 cause a severe speech and language disorder. The gene is transmitted in an autosomal dominant pattern. The following article provides some background to the gene and ...
genetics guide - Ectodermal Dysplasia Society
genetics guide - Ectodermal Dysplasia Society

... Every part of your body is made up of millions of cells. We all began as a single cell, the fertilised egg, that divided into two daughter cells which in turn divided to give four cells and so on. Through this amazing process of embryological development supported by the nurturing environment of our ...
Introduction to sex determination
Introduction to sex determination

... larval stage makes and stores sperm to be used later to fertilize oocytes produced within the gonad of the same animal after spermatogenesis is finished. The embryos produced by self-fertilization are encased in an egg shell and initiate development within the uterus of the hermaphrodite. When they ...
Honors Bio Final Review Sheet
Honors Bio Final Review Sheet

... 31. What is a mutation? Why/how does it have an effect on the whole organism? What does it do to a protein? How does that change an organism’s phenotype or “traits”? 32. What is a chromosome? What is it made of? Where are the genes? 33. For mitosis and meiosis, you may want to download and print dia ...
Hemoglobin: Structure
Hemoglobin: Structure

... new variations. This is one of the crucial pieces of information that Darwin lacked, and thus prevented him from actually directly addressing the name of his book: The Origin of Species (1859). • It was an ongoing criticism of Darwinian evolution until the discoveries of how genetic material can ran ...
The chromosomal theory of inheritance
The chromosomal theory of inheritance

... • Linkage is defined as the tendency of closetogether genes to segregate together  the further two genes are from each other on the same chromosome, the more likely crossing over is to occur between them • this would lead to independent segregation ...
Biology Midterm Review Sheet
Biology Midterm Review Sheet

... 3. Where does photosynthesis occur? 4. What type of organisms carry out photosynthesis? 5. What is the most important energy molecule in organisms? 6. What is the equation for cellular respiration? 7. Where does respiration occur in the cell? ...
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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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