Genetics, 5th Edition. Peter J. Russell, Reed College. © |Pearson | Out of print. Share this page. Genetics, 5th Edition. Cell Division, Genetics, and Molecular Biology Cell Division, Genetics, and Download Book (PDF, KB) Advanced Operators and Techniques in Genetic. Pcopy Genetics 5th Edition by Peter J Russell, , available at Book Depository with free delivery worldwide.
|Language:||English, Spanish, Japanese|
|Genre:||Politics & Laws|
|ePub File Size:||23.76 MB|
|PDF File Size:||12.53 MB|
|Distribution:||Free* [*Sign up for free]|
Russell. Identifier-arkark://t3nw4mt9j. OcrABBYY FineReader Ppi ScannerInternet Archive HTML5 Uploader Year Genetics Book. IdentifierRussellIGenetics. Identifier-arkark://t5pf9m. OcrABBYY FineReader Ppi ScannerInternet Archive. Library of Congress Cataloging-in-Publication Data Russell, Peter J. iGenetics: a .. The book covers all major areas of genetics, balanc- ing classical and.
JUN 24 Beskrivning: i Genetics: A Molecular Approach reflects the dynamic nature of modern genetics by emphasizing an experimental, inquiry-based approach with a solid treatment of many research experiments. The text is ideally suited for students who have had some background in biology and chemistry and who are interested in learning the central concepts of genetics. Problem solving is a major feature of the text and students have the opportunity to apply critical thinking skills to a variety of problems at the end of each chapter. Pedagogical features such as Principal Points, at the beginning of each chapter, and Keynotes, strategically placed throughout the chapter, are useful learning tools. The i Genetics CD-ROM and the companion website contain 25 activities and 59 narrated animations, all of which are based on text figures, to help students visualize complex processes and challenging concepts they encounter in the main text.
This allows researchers to identify and sort males from females. This enables the researchers to identify and sort males from females.
Why is this useful? The ability to rapidly sort mosquitoes makes it possible to produce populations of sterile males and then release the sterile males without the risk of releasing additional females.
The release of sterile males may be an effective means of controlling mosquito populations because females only breed once before they die. Mating with a sterile male prevents a female from producing offspring.
Overall, as we move forward in the twenty-first century, the excitement level in the field of genetics is high, perhaps higher than it has ever been. Nevertheless, the excitement generated by new genetic knowledge and technologies will also create many ethical and societal challenges. In this chapter, we begin with an overview of genetics and then explore the various fields of genetics and their experimental approaches. It stands as the unifying discipline in biology by allowing us to understand how life can exist at all levels of complexity, ranging from the molecular to the population level.
Genetic variation is the root of the natural diversity that we observe among members of the same species as well as among different species.
Genetics is centered on the study of genes.
A gene is classically defined as a unit of heredity, but such a vague definition does not do justice to the exciting characteristics of genes as intricate molecular units that manifest themselves as critical contributors to cell structure and function. At the molecular level, a gene is a segment of DNA that produces a functional product.
The functional product of most genes is a polypeptide, which is a linear sequence of amino acids that folds into units that constitute proteins. In addition, genes are commonly described according to the way they affect traits, which are the characteristics of an organism. In humans, for example, we speak of traits such as eye color, hair texture, and height.
The ongoing theme of this textbook is the relationship between genes and traits. As an organism grows and develops, its collection of genes provides a blueprint that determines its characteristics. In this section of Chapter 1, we examine the general features of life, beginning with the molecular level and ending with populations of organisms. As will become apparent, genetics is the common thread that explains the existence of life and its continuity from generation to generation.
For most students, this chapter should serve as a cohesive review of topics they learned in other introductory courses such as General Biology. Living Cells Are Composed of Biochemicals To fully understand the relationship between genes and traits, we need to begin with an examination of the composition of living organisms. Every cell is constructed from intricately organized chemical substances. Small organic molecules such as glucose and amino acids are produced from the linkage of atoms via chemical bonds.
The chemical properties of organic molecules are essential for cell vitality in two key ways. First, the breaking of chemical bonds during the degradation of small molecules provides energy to drive cellular processes.
A second important function of these small organic molecules is their role as the building blocks for the synthesis of larger molecules. Four important categories of larger cellular molecules are nucleic acids i. Three of these—nucleic acids, proteins, and carbohydrates—form macromolecules that are composed of many repeating units of smaller building blocks.
Proteins, RNA, and carbohydrates can be made from hundreds or even thousands of repeating building blocks. DNA is the largest macromolecule found in living cells.
A single DNA molecule can be composed of a linear sequence of hundreds of millions of nucleotides! The formation of cellular structures relies on the interactions of molecules and macromolecules. For example, nucleotides are the building blocks of DNA, which is a constituent of cellular chromosomes Figure 1.
In addition, the DNA is associated with a myriad of proteins that provide organization to the structure of chromosomes. Within a eukaryotic cell, the chromosomes are contained in a compartment called the cell nucleus. The nucleus is bounded by a double membrane composed of lipids and proteins that shields the chromosomes from the rest of the cell. The organization of chromosomes within a cell nucleus protects the chromosomes from mechanical damage and provides a single compartment for genetic activities such as gene transcription.
As a general theme, the formation of large cellular structures arises from interactions among different molecules and macromolecules. These cellular structures, in turn, are organized to make a complete living cell.
All of the proteins that a cell makes at a given time is called its proteome. The range of functions among different types of proteins is truly remarkable. Some proteins help determine the shape and structure of a given cell. The 3-M syndrome is characterized by pre- and postnatal growth retardation, distinctive facial features relatively large head, frontal bossing, pointed and prominent chin, fleshy and upturned nose, full lips and eyebrows, and a hypoplastic midface , and radiologic abnormalities.
Intelligence is normal. Final height is 5 to 6 SD below the mean.
Characteristic radiologic findings are slender long bones, thin ribs, tall vertebral bodies that become foreshortened over time, spina bifida occulta, small pelvis, small iliac wings, and retarded bone age. Mutation of CUL7 is causative.
Inheritance is autosomal recessive. Children with fetal alcohol syndrome FAS usually have intrauterine growth retardation, microcephaly, failure to thrive, and often triangular facies. For most children with fetal alcohol syndrome in utero exposure to ethanol can be documented and facial findings short palpebral fissures, flat philtrum, and thin upper lip are often distinctive. IMAGe syndrome is characterized by intrauterine growth restriction, metaphyseal dysplasia, adrenal hypoplasia congenita, and genital abnormalities including cryptorchidism and micropenis.
Head circumference is normal [ Vilain et al , Pedreira et al ]. A skeletal survey should be performed to exclude a skeletal dysplasia that may mimic RSS.
Note: Bone age may be delayed in children with RSS; however, delayed bone age is a nonspecific finding frequently seen in children with intrauterine growth retardation from many etiologies. Individuals with RSS have a normal head circumference. When the head circumference is more than 3 SD below the mean, another etiology for growth retardation should be sought.
Management Evaluations Following Initial Diagnosis To establish the extent of disease in an individual diagnosed with Russell-Silver syndrome RSS , the following evaluations are recommended: Assessment and plotting of growth curves. Physical examination for evaluation of possible limb-size asymmetry and oral and craniofacial abnormalities For most children with RSS, evaluation for growth hormone deficiency by standard methods For children with diaphoresis, evaluation for hypoglycemia For children suspected of having gastroesophageal reflux disease GERD , evaluation for esophagitis including barium swallow studies, pH probe, and endoscopy Screening assessment of neurocognitive development, language, and muscle tone Treatment of Manifestations Growth.
These factors can play a significant role in self-image, peer relationships, and socialization. Thus, psychological counseling is frequently helpful for children with RSS. Such treatment is best undertaken in a center with experience in managing growth disorders. One study demonstrated significant increase in height in children with RSS treated with growth hormone, but without a change in body or limb asymmetry [ Rizzo et al ].
A later study looking at both IGF1 and IGF binding protein-3 IGFBP-3 levels revealed no correlation between changes in the levels of these proteins and growth velocity after treatment with growth hormone; however, the diagnosis of RSS was based solely on clinical presentation and no data regarding testing for 11p15 methylation defects or maternal UPD7 were reported [ Beserra et al ].
In a recent long term outcome study of 26 children with RSS treated with growth hormone for a median period of 9. Unfortunately it is difficult to interpret the results of many studies of children with RSS who have received growth hormone, given the known genetic heterogeneity of the disorder and lack of etiologic data included in these studies.
Also, it will be important to look at the long-term effects of growth hormone therapy on children with RSS, especially with respect to influence on final adult height and any possible changes in orthopedic management for those individuals with limb-length asymmetry. Growth hormone deficiency. Treatment with human growth hormone is necessary in the presence of documented growth hormone deficiency. Skeletal abnormalities. Lower-limb length discrepancy exceeding 3 cm can lead to compensatory scoliosis and thus requires intervention.
Initial treatment is use of a shoe lift. In older children, distraction osteogenesis or epiphysiodesis can be considered. Neurodevelopment For infants with hypotonia, referral to an early-intervention program and physical therapist For children with evidence of delay, referral for early intervention and speech and language therapy For school-age children, working with the school system to address learning disabilities through appropriate neuropsychological testing and an individualized educational plan Hypoglycemia should be treated in a standard manner with dietary supplementation, frequent feedings, and use of complex carbohydrates.
Gastrointestinal disorders should be aggressively managed. Treatment of gastroesophageal reflux initially with positioning and thickened feeds is recommended along with use of acid blocking medications preferably proton pump inhibitors such as omeprazole or patoprazole as needed.
Surgical management with fundoplication may be necessary in more severe cases or in instances in which conservative measures are unsuccessful. Craniofacial anomalies. For those children with severe micrognathia or cleft palate, management by a multidisciplinary craniofacial team is recommended. Orthognathic surgery is rarely required.