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Pathchat no 32 Paternity (rev)
Pathchat no 32 Paternity (rev)

... using buccal swabs, blood or any other types of specimens. Humans have 22 matched pairs of autosomal chromosomes and 2 sex determining chromosomes. Paternity testing is performed with markers on the autosomal chromosomes and gender is determined with markers on the sex chromosomes. One chromosome in ...
Genetics Review-
Genetics Review-

... Genetics Review ...
5 BLY 122 Lecture Notes (O`Brien) 2010 II. Protists (Chapter 29) A
5 BLY 122 Lecture Notes (O`Brien) 2010 II. Protists (Chapter 29) A

... 1. Protists are all the eukaryotes that are not fungi, plants, or animals. Picture Slide Fig 29.1 2. Protists are a PARAPHYLETIC group. (See Box 29.1, p. 594) a. In paraphyletic groups, members share characteristics, but do not necessarily share a common ancestor b. Paraphyletic groups are not evolu ...
Gene transfer from organelles to the nucleus: Frequent and in big
Gene transfer from organelles to the nucleus: Frequent and in big

... evidence indicates this to be the case. The Arabidopsis genome revealed 17 different tRNA- and intron-containing insertions of recently integrated chloroplast DNA in nuclear chromosomes, indicating that recombination between nuclear DNA and escaped chloroplast DNA is at work (12). However, only 11 k ...
Chromosome Organization and Dynamics during Interphase, Mitosis
Chromosome Organization and Dynamics during Interphase, Mitosis

... Effects of chromatin organization on gene expression are poorly understood in plants. In Arabidopsis, the majority of genes are located on euchromatic loops stretching out of the chromocenters (Fransz et al., 2002). However, it is unclear if there are particular nucleus regions that are occupied by ...
Slide 1
Slide 1

... Common ancestry of individual nucleotides. If divergence of sequences involved insertions and deletions, nucleotides derived from the same ancestral nucleotide can become shifted. Thus, establishing common ancestry of individual nucleotides from different species requires sequence alignment. Let us ...
Chapter 9 - Genetics
Chapter 9 - Genetics

... • Other organisms have temperaturedependent sex determination! ...
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RECIPROCAL CHROMOSOME TRANSLOCATIONS IN 437
RECIPROCAL CHROMOSOME TRANSLOCATIONS IN 437

... literature, many studies of male infertility due to balanced translocation are reported (Aydos, Tukun 2006, Šeliga et al. 2008a, 2008b). There is an increased risk for males with autosomal abnormalities to have oligospermia, and chromosome studies on spermatozoa show an unbalanced karyotype in varia ...
Midterm #1 Study Guide
Midterm #1 Study Guide

... How are photosynthesis and aerobic respiration linked? MITOSIS What is the difference between mitosis and meiosis? Where do these processes occur? What are the results from each? Proteins associated with DNA in eukaryotes are called ______. Histone–DNA units are called _______. Chromatids that are a ...
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... characterized by in that they follow the Mendelian rules of inheritance. • The study of particular families using linkage analysis has been successful for the Mendelian diseases. • However, the more common complex (i.e. nonMendelian) disorders have been much more difficult to investigate, even there ...
Genetics Power Point
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... the United States. People with Duchenne muscular dystrophy rarely live past their early 20s. The disease is characterized by a progressive weakening of the muscles and loss of coordination. Researchers have traced the disorder to the absence of a key muscle protein called dystrophin and have tracked ...
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... • Mutation occurs as a result of error during the replication of the gene or chromosome. • Somatic mutations that occur in normal body cells cannot be inherited. • Mutations may be inherited by the next generation if they occur in cells that give rise to gametes. ...
Chromosomal changes associated with changes in development
Chromosomal changes associated with changes in development

... glycoprotein genes in Trypanosoma brucei. At the top is a restriction map of the basic copy of the VSG gene 118. In each independently isolated clone of trypanosome expressing the 118 VSG an additional copy can be detected - the ELC. Four such examples are shown. Comparison of the maps show that eac ...
Sex linkage and Pedigrees
Sex linkage and Pedigrees

... Sex determination in mammals  In humans and some other organisms, X and Y chromosomes determine the sex of an individual.  This is because they carry certain genes that are critical in sex determination, such as the SRY gene on the mammalian Y chromosome, which controls testis formation.  Indivi ...
Mutations
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... 1. Deletions: occurs when a chromosome breaks and a piece of a chromosome is lost. ...
Transcription of a genome
Transcription of a genome

... single circular double-stranded molecule. The length of E.coli DNA is 1.4 mm. Human Genome ~ 3 x 109 base pairs of DNA divided into chromosomes that each contain a single, linear doublehelical DNA molecule of ~ 200 x 106 base pairs. Chromosomes are visible only just before cells divide but not in no ...
Heredity Presentation
Heredity Presentation

... Law of Independent Assortment: Each trait has an equal and random chance of being chosen. Only true for genes on different chromosomes. ...
Genes, Inheritance and Genetic Testing
Genes, Inheritance and Genetic Testing

... strand of genetic code called DNA. The DNA is spelt out by a 4-letter alphabet or code. The complete DNA code is 3 billion letters long. Along the strand of DNA are regions called genes. As there are two copies of every chromosome, there are also two copies of every gene (one from each parent). Each ...
localization of histone gene transcripts in newt lampbrush
localization of histone gene transcripts in newt lampbrush

... attempt resulted in the regular labelling of a few pairs of loops on bivalent X and one pair of loops on bivalent I; the second attempt resulted in a far more complex distribution of label over the chromosome complement, altogether too complex to justify a detailed analysis. The first attempt indica ...
Bio 30 Practice Exam
Bio 30 Practice Exam

... 12. Men who have the AZFc deletion and who father children through the ICSI procedure will pass on the infertility trait to A. their sons only B. all their children C. their daughters only D. none of their children ...
Chromosome Organization and Dynamics during Interphase, Mitosis
Chromosome Organization and Dynamics during Interphase, Mitosis

... Effects of chromatin organization on gene expression are poorly understood in plants. In Arabidopsis, the majority of genes are located on euchromatic loops stretching out of the chromocenters (Fransz et al., 2002). However, it is unclear if there are particular nucleus regions that are occupied by ...
Recombinant DNA Techniques Laboratory Bi 431/531
Recombinant DNA Techniques Laboratory Bi 431/531

... • Present in many deep sea organisms and in the open ocean • Most belong to genus Photobacterium, some to Vibrio • The lux operon – 5 genes, about 8 kb – Three genes remove Acyl ACP from fatty acid biosynthesis pathway – Two genes code for the α and ß subunits of luciferase ...
DNA and Chromatin
DNA and Chromatin

... As shown above, adding methyl moieties to lysine does not change the charge of lysine. However, it can still result in a change of chromatin architecture. For instance, H3K4me3 (three methyl groups on the fourth lysine of histone H3) is a hallmark of transcriptional activity (loose chromatin structu ...
Lac A
Lac A

... Normal Zigote: normal phenotype ...
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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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