Introduction
1. The Grainyhead (Grh) gene family
Grainyhead (Grh) genes are conserved in metazoans. They encode a family of transcription factors with a unique, unusually large, DNA-binding and dimerization domain, and an isoleucine-rich activation domain(Attardi and Tjian, 1993; Gustavsson et al., 2008; Moussian and Uv, 2005; Ting et al., 2003b; Uv et al., 1994; Venkatesan et al., 2003; Wilanowski et al., 2002). Grh factors were first identified in Drosophila (Bray et al., 1989; Bray and Kafatos, 1991; Dynlacht et al., 1989; Johnson et al., 1989) and since then, they were also found in animals as diverse as nematodes and humans. Grh proteins have not yet been detected in unicellular organisms. Phylogenetic analysis subdivides this gene family into two main classes, the Grh-like sub-family and the CP2 sub-family, depending whether the family members are more related to the Drosophila grh, or to another Drosophila gene, CP2 (Ting et al., 2003b; Venkatesan et al., 2003; Wilanowski et al., 2002). The fly and worm genomes each contain a single grh gene. Mammals, both mice and humans, have evolved three Grh homologues: Grh-like-1 (Grhl-1, or Mammalian Grainyhead (MGR)/TFCP2L2), Grhl-2 (Brother-of-MGR (BOM)/TFCP2L3) and Grhl-3 (Sister-of-MGR (SOM)/ TFCP2L4). This group of genes encodes proteins with highly homologous DNA-binding and dimerization domains. They all show restricted expression pattern during embryogenesis and play important roles in organogenesis and epidermal
The motivation of this lab report is to use Mendel’s Laws of Inheritance to analyze and predict the genotypes and phenotypes of an offspring generation (F2) after knowing the genotypes and phenotypes of the parent generation (F1). The hypothesis for this experiment is that the mode of inheritance for the shaven bristle allele in flies is autosomal recessive in both male and female flies.
The closest neighboring gene to mine is named growth factor independent 1B transcription repressor (GFI1B), and it codes for Zinc finger protein Gfi-1b.
The goal of this study was to induce a deletion in the DMAP1 gene on chromosome two in Drosophila melanogaster through P-element mobilization. The DMAP1 gene may be an essential gene, however not much is known about it. We attempted to uncover the function of DMAP1 by creating a series of genetic crosses and selecting for brown-eyed non-stubble male flies that may have the deletion. To test whether these flies had the deletion, we produced PCR products and ran them on an agarose gel, which resulted as inconclusive. We created a balanced stock of flies homozygous for the deletion to see if the
MacKay JO, Soanes KH, Srivastava A, Simmonds A, Brook WJ, Bell JB. An in vivo analysis of the vestigial gene in Drosophila melanogaster defines the domains required for Vg function. Genetics. 2003;163(4):1365-1373.
DNA contains the information that builds our bodies from a single fertilized egg. Cellular diversity gives rise to our tissues and organs, with distinct shapes and functions. Yet, all cells in our body contain exactly the same DNA. The resolution to this apparent paradox lies in the fact that different pieces of DNA are turned on in every cell, and these pieces are called genes. When a gene is turned on, It makes a protein that affects what the cell looks like and how it behaves. Our bodies are a composition of individual genes turning on and off inside each cell during our development. We use this information about gene “switches” to compare the activity of different genes, with the end goal of assessing what kinds of changes are involved in the origin of new organs. For limbs, we catalogue the genetic differences between fins and mammalian limbs. Then, we study the function of these genes in embryos and do experiments to manipulate genes, mutate specimens, and observe the responses to these changes. Each gene has a distinctive sequence, and using molecular tools, researches can scan another species’ DNA for identical sequences. It turns out that the DNA “recipe” to build upper arms, forearms, wrists, and digits is identical in every creature that has
SUFFOLK COUNTY COMMUNITY COLLEGE MICHAEL J. GRANT CAMPUS, BRENTWOOD NY BIO 150—MODERN BIOLOGY I INSTRUCTOR: DR. JAMES F. REMSEN, JR. ADDENDUM TO COURSE OUTLINE Instructor email: remsenj@sunysuffolk.edu Phone: (631) 851-6824 Office: Sagtikos 110 Office Hours Spring 2013: M Tu Th 11:00 A.M.-12:15 P.M. W 6:00-7:15 P.M. (Virtual) This addendum addresses how I run my classroom and what I expect of students above and beyond what is presented in the syllabus. I also offer tips for success in the course, and advice to help you determine if this course will meet your career goals once you complete it. Please take this information in the spirit in which it is offered: to foster a better learning environment, and to help you avoid outcomes that are
Molecular Cell Biology, 7th Edition, 2013, Lodish, Berk, Kaiser, Krieger, Bretscher. Ploegh, Amon, and Scott. W.H. Freeman and Company (ISBN-13: 978-1-4292-3413-9)
insect, we still have to have a backbone in which we can actually add that gene towards. For
Freeman, S., Black, M., Taylor, E., Monroe, J., Allison, L., Podgorski, G.,… Quillin, K. (2013, January 18) Biological Science 5th edition. Chapter 7 pages
The fruit fly, Drosophila melanogaster, became an important model organism for the study of human genetics and for the establishment of more biological principles (Roberts 2006). This organism became a good candidate to work with because of its short life cycle, its inexpensiveness, small size, its genetic variability, easily cultured and its ability to produce many offspring. Nichols and Phandey made an important discovery: approximately 75% of disease-causing genes in humans are homologous to genes found in Drosophila melanogaster (Russell and Tickoo). This is an important observation, because it made it possible to discover treatments for human diseases. For example, the fly has a tumor gene homologous to the human LATS1 gene.
Campbell, Neil A., Jane B. Reese, Martha R. Taylor, Eric J. Simon. Biology 105 Taken From; Biology: Concepts & Connections (Fifth Edition) Benjamin Cumming, San Francisco, CA, 2013.
Gain of function (ectopic expression in the developing haltere epithelium) of each of these genes changes the haltere of the fly into a second set of wings: double-wings phenotype (GOF).
The second stage occurs during the outward growth of the distal limb regions which depends greatly on sonic hedgehog expression at week 6 day 52 is when hand is fully formed. In both stages HOXD genes are critical since they are involved in initiation of shh expression during the earlier stage and mediation of shh signaling from within the limbs during the second stage. The resulting phenotype of HOXD13 mutants display limb malformations. There is much fewer missense and nonsense mutations in HOXD13 and the most common mutation is the addition of 7-14 in the N-terminal polyalanine repeats of the HOXD13 gene. When the gene is abnormal from the polyalanine repeat mutation, it produces an abnormal protein which destabilizes the normal protein confirmation, causing aggregation. Once this occurs, it halts the protein translocation which occurs from the cytoplasm to the nucleus where it acts as a transcription factor. Additionally, the size of the polyalanine repeats directly correlates with the severity of
Homeobox genes act as transcription factors, found in eukaryotes. Homeobox genes are associated with many body structures such as the central nervous system, neural crest, skeleton muscle, heart, brain, and liver (1). Homeobox genes are highly conservative and consist of 180 base pairs. Homeobox genes had isolated from Xenopus, mouse, and humans. In the human genome, there are about 255 homeobox genes (1). The well-known homeobox gene is HOX gene. Such a mutation in one of these genes leads to phenotype alterations. This paper provides an overview about one of Hox genes, which is MSX1 (2).
What does it mean to be a man? Some say it’s your age that determines whether or not you are a man, or it could be your maturity. Well, it's much more than that.