The cold-sensitive period for frizzled in the development of wing hair polarity ends prior to the start of hair morphogenesis

1994 ◽  
Vol 46 (2) ◽  
pp. 101-107 ◽  
Author(s):  
Paul N. Adler ◽  
Jeannette Charlton ◽  
Katherine H. Jones ◽  
Jingchun Liu
Genetics ◽  
1994 ◽  
Vol 137 (3) ◽  
pp. 829-836 ◽  
Author(s):  
P N Adler ◽  
J Charlton ◽  
W J Park

Abstract The adult cuticular wing of Drosophila is covered with an array of distally pointing hairs. Mutations in the inturned (in) gene result in both abnormal hair polarity (i.e., hairs no longer point distally), and, in most cells forming more than one hair. We have isolated and characterized a collection of in alleles. Among this collection of alleles are a number of rearrangements that enable us to assign in to 77B3-5. Almost all of the in alleles, including putative null alleles, result in a stronger phenotype on the wing at 18 degrees than 29 degrees. The data argue that the in-dependent process is cold-sensitive. Temperature shift experiments with a hypomorphic allele show that this cold sensitivity can be relieved by several hours of incubation at the permissive temperature at a variety of times in the early pupae, but that this ability ends prior to the start of hair morphogenesis. One new allele showed a dramatic heat sensitivity. Temperature shift experiments with this allele revealed a very short temperature-sensitive period that is a few hours prior to the start of hair morphogenesis. That the temperature during hair morphogenesis is irrelevant for the phenotype of in is consistent with the hypothesis that the only role that in has in wing hair development is to regulate the initiation of hair morphogenesis.


2005 ◽  
Vol 16 (8) ◽  
pp. 3620-3631 ◽  
Author(s):  
Gregory M. Guild ◽  
Patricia S. Connelly ◽  
Linda Ruggiero ◽  
Kelly A. Vranich ◽  
Lewis G. Tilney

Actin filament bundles can shape cellular extensions into dramatically different forms. We examined cytoskeleton formation during wing hair morphogenesis using both confocal and electron microscopy. Hairs elongate with linear kinetics (∼1 μm/h) over the course of ∼18 h. The resulting structure is vividly asymmetric and shaped like a rose thorn—elongated in the distal direction, curved in two dimensions with an oval base and a round tip. High-resolution analysis shows that the cytoskeleton forms from microvilli-like pimples that project actin filaments into the cytoplasm. These filaments become cross-linked into bundles by the sequential use of three cross-bridges: villin, forked and fascin. Genetic loss of each cross-bridge affects cell shape. Filament bundles associate together, with no lateral membrane attachments, into a cone of overlapping bundles that matures into an oval base by the asymmetric addition of bundles on the distal side. In contrast, the long bristle cell extension is supported by equally long (up to 400 μm) filament bundles assembled together by end-to-end grafting of shorter modules. Thus, bristle and hair cells use microvilli and cross-bridges to generate the common raw material of actin filament bundles but employ different strategies to assemble these into vastly different shapes.


1998 ◽  
Vol 111 (7) ◽  
pp. 887-896 ◽  
Author(s):  
E. Mathe ◽  
I. Boros ◽  
K. Josvay ◽  
K. Li ◽  
J. Puro ◽  
...  

The three dominant TomajD and their eleven revertant (TomajR) alleles have been localized to the alpha Tubulin67C gene of Drosophila melanogaster. Although the meiotic divisions are normally completed in eggs laid by TomajD/+, TomajD/-, TomajR/- females, embryogenesis arrests prior to the gonomeric division. The arrest is caused by: (1) the failure of prominent sperm aster formation; and (2) a consequent lack of female pronuclear migration towards the male pronucleus. Concomitant with the sperm aster defect, the four female meiotic products fuse (tetra-fusion), similar to what is seen in eggs of wild-type virgin females. In eggs of females heterozygous for weaker TomajR alleles, embryogenesis comes to a cessation before or shortly after cortical migration of cleavage nuclei. The apparent source of embryonic defect is the cleavage spindle apparatus. One of the three TomajD alleles is cold-sensitive and its cold-sensitive period coincides with the completion of female meiosis and pronuclear migration. Disorganized central and peripheral nervous systems are also characteristic of embryos derived from the temperature-sensitive TomajD/+ females. The Tomaj mutant phenotypes indicate an involvement of the normal alpha Tubulin67C gene product in: (1) the formation of the sperm aster; (2) cleavage spindle apparatus formation/function; and (3) the differentiation of the embryonic nervous system. The TomajD alleles encode a normal-sized alpha Tubulin67C isotype. Sequence analyses of the TomajD alleles revealed the replacement in different positions of a single negatively charged or neutral amino acid with a positively charged one. These residues presumably identify important functional sites.


Genome ◽  
1996 ◽  
Vol 39 (2) ◽  
pp. 459-464 ◽  
Author(s):  
Ralph M. Hecht ◽  
Mary A. Norman ◽  
Tammy Vu ◽  
William Jones

A set of uncoordinated (Unc) cold-sensitive (cs) mutants was isolated at a stringent condition of 11 °C. About half of the 13 independently isolated cs-Unc mutants were alleles of three X-linked Unc mutants that exhibited the "kinker" phenotype. The remaining four isolates identified new mutants that exhibited "kinker," "coiler," or severe paralytic phenotypes. The temperature-sensitive period (TSP) for each gene was determined. As a homozygous or heterozygous dominant, unc-125 exhibited a TSP throughout all stages of development. Its severe paralysis was immediately observed upon a shift down to 11 °C and reversed upon a shift up to 23 °C. The reversible thermolability of the unc-125 gene product indicated that it may function in a multicomponent process involved in neuro-excitation. Key words : Caenorhabditis elegans, cold-sensitive uncoordinated mutants, cs-Unc.


Genetics ◽  
1974 ◽  
Vol 76 (3) ◽  
pp. 511-536
Author(s):  
Theodore R F Wright

ABSTRACT The X-linked, cold-sensitive zygotic lethal, l(1)TW-6cs, both in homozygous and heterozygous females, induces nondisjunction of all four chromosomes at Meiosis I at both 25° and 17°. Nondisjunction frequencies approaching 0.5 for the X and fourth chromosomes have been observed at 16°–18°. The disjunction of the X chromosomes in males is not affected. The mutant causes mitotic irregularities in zygotes at both 25° and 17°. Mortality of all zygotes produced by the crosses 6cs/6cs × 6cs/BsY and FM7/6cs × 6cs/BsY is respectively 86% and 67–74% at 25° and 99.8–99.9% and 94% at 17°. The mortality of 6cs hemizygotes derived from females carrying no doses of 6cs (C(1)DX,y f/y × 6cs/BsY) is 45–55% at 25° and 98% at 17°. The length of the temperature-sensitive period for 6cs homo- and hemizygotes is affected by the maternal dosage of 6cs; the shortest TSP is for zero and the longest is for two maternal doses. Mortality takes place primarily during embryogenesis with some larval and little pupal mortality. Analysis of sectioned embryos indicates that the large array of different patterns of damage observed could have arisen from abnormal cleavage divisions and the incomplete population of the blastoderm with nuclei.


Genetics ◽  
2005 ◽  
Vol 172 (3) ◽  
pp. 1643-1653 ◽  
Author(s):  
Nan Ren ◽  
Biao He ◽  
David Stone ◽  
Sreenatha Kirakodu ◽  
Paul N. Adler

2020 ◽  
Vol 5 (6) ◽  
pp. 1767-1775
Author(s):  
Martha S. Burns

Purpose Adolescence is a period of substantial neurophysiological and behavioral growth, representing a second sensitive period of brain development. It is a psychological and social transition period between childhood and adulthood with many beneficial changes occurring, especially with respect to potential responsiveness to clinical intervention. However, adolescent behavioral complexities introduce clinical challenges as well. The purpose of this review article is to review the current neuroimaging research on neurophysiological changes observed during adolescence and the cognitive and social behavioral counterparts, with specific attention to the clinical implications. The review article will then summarize currently available intervention tools that can be utilized by speech-language pathologists working with this population. It will conclude with available evidence-based social-communication approaches that may be applicable as well as available evidence-based supplemental technological cognitive interventions that may be useful in working with adolescents who exhibit language and communication issues. Conclusion As a transition period between childhood and adulthood, adolescence represents a second sensitive period during which there is opportunity for clinically derived beneficial cognitive and communication growth.


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