123 research outputs found

    Limb patterning: from signaling gradients to molecular oscillations

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    The developing forelimb is patterned along the proximal-distal and anterior-posterior axes by opposing gradients of retinoic acid and fibroblast growth factors and by graded sonic hedgehog signaling, respectively. However, how coordinated patterning along both axes is accomplished with temporal precision remains unknown. The limb molecular oscillator hairy2 was recently shown to be a direct readout of the combined signaling activities of retinoic acid, fibroblast growth factor and sonic hedgehog in the limb mesenchyme. Herein, an integrated time-space model is presented to conciliate the progress zone and two-signal models for limb patterning. We propose that the limb clock may allow temporal information to be decoded into positional information when the distance between opposing signaling gradients is no longer sufficient to provide distinct cell fate specification.C.J.S. was supported by Fundacao para a Ciencia e a Tecnologia, Portugal (grant SFRH/BPD/89493/2012); R.P.A. is funded by Ciencia 2007 Program Contract (Portuguese Government) and Programa Operacional Regional do Norte (ON.2) NORTE-07-0124-FEDER-000017. This work was supported by research grants from Institute for Biotechnology and Bioengineering/Centro de Biomedicina Molecular e Estrutural, LA (to I.P.), by the national Portuguese funding through Fundacao para a Ciencia e a Tecnologia (National and FEDER COMPETE Program funds: PTDC/SAU-OBD/099758/2008 and PTDC/SAU-BID/121459/2010 to I.P. and R.P.A., respectively) and by PEst-OE/EQB/LA0023/2011

    Design of Filter Using MOS Current Mode Logic

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    MCML (MOS Current Mode Logic) is a method used for the purpose of reducing the delay and power of the circuit. In high speed application this method is used to reduce the power. In this method the sleep transistor is inserted in series with the supply voltage (or) current source to reduce the power. Different power gating techniques are been used to reduce the static power and to improve the speed and efficiency of the circuit. In this paper, the filter can be designed by using MCML logic. The fourth order band pass filter by using MCML logic is introduced. In order to reduce the power and delay this method is proposed

    An Improved Integrity-Based Hybrid Multi-User Data Access Control for Cloud Heterogeneous Supply Chain Databases

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    Cloud-based supply chain applications play a vital role in the multi-user data security framework for heterogeneous data types. The majority of the existing security models work effectively on small to medium-sized datasets with a homogenous data structure. In contrast, Supply Chain Management (SCM) systems in the real world utilize heterogeneous databases. The heterogeneous databases include a massive quantity of raw SCM data and a scanned image of a purchase quotation. In addition, as the size of the database grows, it becomes more challenging to provide data security on multi-user SCM databases. Multi-user datatypes are heterogeneous in structure, and it is complex to apply integrity and confidentiality models due to high computational time and resources. Traditional multi-user integrity algorithms are difficult to process heterogeneous datatypes due to computational time and variation in hash bit size. Conventional attribute-based encryption models such as "Key-policy attribute-based encryption" (KP-ABE), "Ciphertext-Policy Attribute-Based Encryption" (CP-ABE) etc., are used to provide strong data confidentiality on large textual data. Providing security for heterogeneous databases in a multi-user SCM system requires a significant computational runtime for these conventional models. An enhanced integrity-based multi-user access control security model is created for heterogeneous databases in the cloud infrastructure to address the problems with heterogeneous SCM databases. A non-linear integrity model is developed to provide strong integrity verification in the multi-user communication process. A multi-user based access control model is implemented by integrating the multi-user hash values in the encoding and decoding process. Practical results proved that the multi-user non-linear integrity-based multi-access control framework has better runtime and hash bit variation compared to the conventional models on large cloud-based SCM databases

    Free energy barrier for melittin reorientation from a membrane-bound state to a transmembrane state

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    An important step in a phospholipid membrane pore formation by melittin antimicrobial peptide is a reorientation of the peptide from a surface into a transmembrane conformation. In this work we perform umbrella sampling simulations to calculate the potential of mean force (PMF) for the reorientation of melittin from a surface-bound state to a transmembrane state and provide a molecular level insight into understanding peptide and lipid properties that influence the existence of the free energy barrier. The PMFs were calculated for a peptide to lipid (P/L) ratio of 1/128 and 4/128. We observe that the free energy barrier is reduced when the P/L ratio increased. In addition, we study the cooperative effect; specifically we investigate if the barrier is smaller for a second melittin reorientation, given that another neighboring melittin was already in the transmembrane state. We observe that indeed the barrier of the PMF curve is reduced in this case, thus confirming the presence of a cooperative effect

    dyschronic, a Drosophila Homolog of a Deaf-Blindness Gene, Regulates Circadian Output and Slowpoke Channels

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    Many aspects of behavior and physiology are under circadian control. In Drosophila, the molecular clock that regulates rhythmic patterns of behavior has been extensively characterized. In contrast, genetic loci involved in linking the clock to alterations in motor activity have remained elusive. In a forward-genetic screen, we uncovered a new component of the circadian output pathway, which we have termed dyschronic (dysc). dysc mutants exhibit arrhythmic locomotor behavior, yet their eclosion rhythms are normal and clock protein cycling remains intact. Intriguingly, dysc is the closest Drosophila homolog of whirlin, a gene linked to type II Usher syndrome, the leading cause of deaf-blindness in humans. Whirlin and other Usher proteins are expressed in the mammalian central nervous system, yet their function in the CNS has not been investigated. We show that DYSC is expressed in major neuronal tracts and regulates expression of the calcium-activated potassium channel SLOWPOKE (SLO), an ion channel also required in the circadian output pathway. SLO and DYSC are co-localized in the brain and control each other's expression post-transcriptionally. Co-immunoprecipitation experiments demonstrate they form a complex, suggesting they regulate each other through protein–protein interaction. Furthermore, electrophysiological recordings of neurons in the adult brain show that SLO-dependent currents are greatly reduced in dysc mutants. Our work identifies a Drosophila homolog of a deaf-blindness gene as a new component of the circadian output pathway and an important regulator of ion channel expression, and suggests novel roles for Usher proteins in the mammalian nervous system

    Recruitment of a SAP18-HDAC1 Complex into HIV-1 Virions and Its Requirement for Viral Replication

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    HIV-1 integrase (IN) is a virally encoded protein required for integration of viral cDNA into host chromosomes. INI1/hSNF5 is a component of the SWI/SNF complex that interacts with HIV-1 IN, is selectively incorporated into HIV-1 (but not other retroviral) virions, and modulates multiple steps, including particle production and infectivity. To gain further insight into the role of INI1 in HIV-1 replication, we screened for INI1-interacting proteins using the yeast two-hybrid system. We found that SAP18 (Sin3a associated protein 18 kD), a component of the Sin3a-HDAC1 complex, directly binds to INI1 in yeast, in vitro and in vivo. Interestingly, we found that IN also binds to SAP18 in vitro and in vivo. SAP18 and components of a Sin3A-HDAC1 complex were specifically incorporated into HIV-1 (but not SIV and HTLV-1) virions in an HIV-1 IN–dependent manner. Using a fluorescence-based assay, we found that HIV-1 (but not SIV) virion preparations harbour significant deacetylase activity, indicating the specific recruitment of catalytically active HDAC into the virions. To determine the requirement of virion-associated HDAC1 to HIV-1 replication, an inactive, transdominant negative mutant of HDAC1 (HDAC1H141A) was utilized. Incorporation of HDAC1H141A decreased the virion-associated histone deacetylase activity. Furthermore, incorporation of HDAC1H141A decreased the infectivity of HIV-1 (but not SIV) virions. The block in infectivity due to virion-associated HDAC1H141A occurred specifically at the early reverse transcription stage, while entry of the virions was unaffected. RNA-interference mediated knock-down of HDAC1 in producer cells resulted in decreased virion-associated HDAC1 activity and a reduction in infectivity of these virions. These studies indicate that HIV-1 IN and INI1/hSNF5 bind SAP18 and selectively recruit components of Sin3a-HDAC1 complex into HIV-1 virions. Furthermore, HIV-1 virion-associated HDAC1 is required for efficient early post-entry events, indicating a novel role for HDAC1 during HIV-1 replication

    Pitfalls in machine learning‐based assessment of tumor‐infiltrating lymphocytes in breast cancer: a report of the international immuno‐oncology biomarker working group

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    The clinical significance of the tumor-immune interaction in breast cancer (BC) has been well established, and tumor-infiltrating lymphocytes (TILs) have emerged as a predictive and prognostic biomarker for patients with triple-negative (estrogen receptor, progesterone receptor, and HER2 negative) breast cancer (TNBC) and HER2-positive breast cancer. How computational assessment of TILs can complement manual TIL-assessment in trial- and daily practices is currently debated and still unclear. Recent efforts to use machine learning (ML) for the automated evaluation of TILs show promising results. We review state-of-the-art approaches and identify pitfalls and challenges by studying the root cause of ML discordances in comparison to manual TILs quantification. We categorize our findings into four main topics; (i) technical slide issues, (ii) ML and image analysis aspects, (iii) data challenges, and (iv) validation issues. The main reason for discordant assessments is the inclusion of false-positive areas or cells identified by performance on certain tissue patterns, or design choices in the computational implementation. To aid the adoption of ML in TILs assessment, we provide an in-depth discussion of ML and image analysis including validation issues that need to be considered before reliable computational reporting of TILs can be incorporated into the trial- and routine clinical management of patients with TNBC
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