Rachis extension in drp-1(or1393ts) mutants and GFP::DRP-1 localization. Rachis extension in drp-1(or1393ts) mutants and GFP::DRP-1 localization. (A) The.

Slides:



Advertisements
Similar presentations
Studies of protein trap expression We compared the apparent intensity of GFP-protein staining in the GSCs with the RNA level of the corresponding gene.
Advertisements

Membrane topology prediction of the SLC45A2 protein using TMHMM (v. 2
Phenotypic analysis of spo73∆ mutant.
Volume 20, Issue 5, Pages (May 2011)
David J. Katz, T. Matthew Edwards, Valerie Reinke, William G. Kelly 
Tony DeFalco, Nicole Camara, Stéphanie Le Bras, Mark Van Doren 
A bHLH Code for Sexually Dimorphic Form and Function of the C
Volume 109, Issue 11, Pages (December 2015)
H3 Dynamics in Wild-Type and fas1-4 Mutant Roots.
Volume 27, Issue 6, Pages (March 2017)
Volume 12, Issue 4, Pages (April 2007)
LET-418/Mi2 and SPR-5/LSD1 Cooperatively Prevent Somatic Reprogramming of C. elegans Germline Stem Cells  Stéphanie Käser-Pébernard, Fritz Müller, Chantal.
Clone patterns and frequencies produced by lines 168 and 688A.
Volume 15, Issue 24, Pages (December 2005)
Volume 29, Issue 4, Pages (February 2008)
nrde-3-dependent silencing of endogenous RNAi targets and transgenes.
The GSL biosynthetic pathway is active in both germ line and follicle cells. The GSL biosynthetic pathway is active in both germ line and follicle cells.
Volume 87, Issue 2, Pages (October 1996)
3′ UTRs Are the Primary Regulators of Gene Expression in the C
X-Chromosome Inactivation Patterns Are Unbalanced and Affect the Phenotypic Outcome in a Mouse Model of Rett Syndrome  Juan I. Young, Huda Y. Zoghbi 
IVA can localize to and encase the forespore in the absence of VM
Time course of Fim1-GFP appearance and disappearance in actin patches.
Volume 12, Issue 5, Pages (March 2002)
Stephanie C. Weber, Clifford P. Brangwynne  Current Biology 
Sex, Not Genotype, Determines Recombination Levels in Mice
Volume 97, Issue 12, Pages (December 2009)
Global Transcriptional Repression in C
Direct role of HIS-24 and HPL in control of microbial resistance.
Volume 15, Issue 21, Pages (November 2005)
Volume 80, Issue 6, Pages (December 2013)
Volume 1, Issue 2, Pages (August 2001)
The C. elegans Glycopeptide Hormone Receptor Ortholog, FSHR-1, Regulates Germline Differentiation and Survival  Saeyoull Cho, Katherine W. Rogers, David S.
Intrinsic role of Aub in GSC self‐renewal and differentiation
Volume 20, Issue 5, Pages (May 1998)
Volume 6, Issue 4, Pages (April 2004)
Volume 3, Issue 5, Pages (November 2002)
Immunohistochemical analysis of individual StanEx enhancer trap line expression in larval brain and VNC. Third larval instar CNS and VNC expression of.
Loss of FZR-1 results in elevated SAS-5 levels.
T7 transcripts increase relative to E. coli transcripts over time.
GON-1 and Fibulin Have Antagonistic Roles in Control of Organ Shape
Figure 3 ADAM22 mutant proteins do not bind to LGI1
Distribution of deletions and insertions in the ade6-(GACC)7ΔT repeat.
Distinct requirements for Kita and Mitfa.
Biochemical properties and expression profile of KCC2-pHext and its mutants with truncated N and C termini. Biochemical properties and expression profile.
DEcad::αCat rescues of α-Cat mutant defects.
Expression of FOZI-1 in different M lineage mutants.
Effects of cgh-1 RNAi on oogenesis and spermatogenesis.
Structure of the C. elegans hermaphrodite germline and expression of cgh-1 mRNA. Structure of the C. elegans hermaphrodite germline and expression of cgh-1.
Oocyte polarity is disrupted in the presence of FP41 mutant PFCs
(A) yellow cDNA comparison among wild-type and ch mutants
Eff localizes in many bands and interbands of wild-type polytene chromosomes. Eff localizes in many bands and interbands of wild-type polytene chromosomes.
Morphological alterations of the brain in Sox2β-geo/ΔENH mutants.
Two domains of KHC act to position the nucleus.
Shp2 is required for lens and lacrimal gland development.
Prophase nuclear movements in wild-type, rec8 and rec7 mutant cells.
Lar function is not required for Stat92E accumulation in GSCs
Abnormal adherens junctions between hub cells and GSCs in Lar mutants.
Apc2 localization and centrosome orientation are altered in Lar mutant GSCs. (A-B′) Apc2 (white, A,B; red, A′,B′) localization in wild-type (A,A′) and.
FRAP and FLIP analysis of GFP-ADAR2 and GFP-ADAR1C-Term.
Volume 27, Issue 6, Pages (March 2017)
Localization of wild-type and mutant FHOD1 at cellular actin structures. Localization of wild-type and mutant FHOD1 at cellular actin structures. Two cell.
Fig. 3. MO-mediated smc3 knockdown results in reduced regenerate length, segment length and cell proliferation. MO-mediated smc3 knockdown results in reduced.
Ultrastructure of the sciatic nerve from P60 and P75 control and Miz1ΔPOZ animals reveal signs of demyelination and dysmyelination. Ultrastructure of the.
MFN2 mutants induce abnormal mitochondrial clustering and morphology in cell bodies and proximal axons. MFN2 mutants induce abnormal mitochondrial clustering.
Muscle microprocesses and contacts between myotubes and axons in E15 intercostal muscle. Muscle microprocesses and contacts between myotubes and axons.
TDIF-Sensitive Xylem Formation in wox4 Mutants
ZCWPW1 expression and dynamic localization in meiotic germ cells
GATOR1 is required to maintain baseline levels of TORC1 activity in Drosophila. GATOR1 is required to maintain baseline levels of TORC1 activity in Drosophila.
Sfr1 localizes broadly throughout the basal body microtubule scaffold
Developmental Timing in C
Presentation transcript:

Rachis extension in drp-1(or1393ts) mutants and GFP::DRP-1 localization. Rachis extension in drp-1(or1393ts) mutants and GFP::DRP-1 localization. (A) The rachis appears to extend to the most mature oocyte (arrowheads) in an adult drp-1(or1393ts) mutant gonad, as detected using mCherry::PH to mark the membranes. (B) ANI-2::GFP localizes to the surface of the rachis (Maddox et al. 2005), which terminates just after the turn in wild-type hermaphrodites. The rachis again extends proximally in an adult drp-1(or1393ts) mutant gonad (arrowheads). (C and D) GFP::DRP-1 (see Materials and Methods) does not localize to openings to the rachis in the distal gonad or to the rachis more proximally, arguing against a direct role in oocyte cellularization. (C) An orthogonal view of the meiotic germ cell openings to the rachis of wild-type strains carrying either ANI-2::GFP or GFP::DRP-1. GFP::DRP-1 does not localize to the germ cell opening (arrows). (D) A view in the plane of the meiotic germ cell openings from the rachis surface. Solid white lines in (C) and (D) mark insets, and dashed white lines indicate individual germ cells with openings to rachis. Josh Lowry et al. G3 2015;5:2241-2255 ©2015 by Genetics Society of America