Task-switching Cost and Intrinsic Functional Connectivity in the Human Brain: Toward Understanding Individual Differences in Cognitive Flexibility

The human ability to flexibly alternate between tasks (i.e., task-switching) represents a critical component of cognitive control. Many functional magnetic resonance imaging (fMRI) studies have explored the neural basis of the task-switching. However, no study to date has examined how individual differences in intrinsic functional architecture of the human brain are related to that of the task-switching. In the present study, we took 11 task-switching relevant areas from a meta-analysis study as the regions of interests (ROIs) and estimated their intrinsic functional connectivity (iFC) with the whole brain. This procedure was repeated for 32 healthy adults based upon their fMRI scans during resting-state (rfMRI) to investigate the correlations between switching cost and the iFC strength across these participants. This analysis found that switch cost was negatively correlated with a set of iFC involved ROIs including left inferior frontal junction, bilateral superior posterior parietal cortex, left precuneus, bilateral inferior parietal lobule, right middle frontal gyrus and bilateral middle occipital gyrus. These connectivity profiles represent an intrinsic functional architecture of task-switching where the left inferior frontal junction plays a hub role in this brain-behavior association. These findings are highly reproducible in another validation independent sample and provide a novel perspective for understanding the neural basis of individual differences in task-switching behaviors reflected in the intrinsic architecture of the human brain.     

Intrinsic Functional Brain Architecture Derived from Graph Theoretical Analysis in the Human Fetus

The human brain undergoes dramatic maturational changes during late stages of fetal and early postnatal life. The importance of this period to the establishment of healthy neural connectivity is apparent in the high incidence of neural injury in preterm infants, in whom untimely exposure to ex-uterine factors interrupts neural connectivity. Though the relevance of this period to human neuroscience is apparent, little is known about functional neural networks in human fetal life. Here, we apply graph theoretical analysis to examine human fetal brain connectivity. Utilizing resting state functional magnetic resonance imaging (fMRI) data from 33 healthy human fetuses, 19 to 39 weeks gestational age (GA), our analyses reveal that the human fetal brain has modular organization and modules overlap functional systems observed postnatally. Age-related differences between younger (GA <31 weeks) and older (GA≥31 weeks) fetuses demonstrate that brain modularity decreases, and connectivity of the posterior cingulate to other brain networks becomes more negative, with advancing GA. By mimicking functional principles observed postnatally, these results support early emerging capacity for information processing in the human fetal brain. Current technical limitations, as well as the potential for fetal fMRI to one day produce major discoveries about fetal origins or antecedents of neural injury or disease are discussed.     

Functional Brain Asymmetry and Individual Differences in Hand Preference in Early Ontogeny

This work was aimed at studying the brain mechanisms of hand preference in 10- to 11-month-old infants. According to the results of neuropsychological investigations, the preference for the right hand in children of this age (at the populational level) primarily arises in actions that demand involvement of the functions of planning and motor control of reaching (functions of the motor control of reaching: FMCR) for an object. The stage of development of the FMCR in each child was scored on the Diamond scale. Total numbers of movements performed by the right and left hands and a coefficient of the manual asymmetry (AC) were calculated. On the basis of quartile analysis of the AC distribution, groups of right-handers, left-handers, and ambidextrals were formed. The EEG was recorded in the state of visual focused attention, and the spectral absolute amplitude density (AAD) of the sensorimotor rhythm and other infant EEG rhythms in the frequency band was analyzed. In order to estimate the statistical correlation of manual asymmetry, gender, and stage of development of the FMCR with functional asymmetry of the AAD of the -band rhythms in different cortical derivations, analysis of variance with factors of repeated measurements and analysis of multiple regression were used. The main results showed that 10- to 11-month-old children with different types of manual asymmetry differed in interhemispheric asymmetry of the visual attention-related EEG -band rhythms (including asymmetry of the sensorimotor rhythm). The maximum differences were observed in the lateral frontal and posterotemporal areas of the brain cortex. The leftward amplitude asymmetry was characteristic of right-handers; in left-handers and ambidextrals, the EEG amplitude was distributed over the brain hemispheres in a more symmetric way. The correlation between the brain and manual asymmetries was stronger in boys than in girls. There was a strict linear correlation between the degree of manual asymmetry and interhemispheric asymmetry of the EEG sensorimotor rhythm in the precentral and lateral frontal brain areas. On the whole, the close correlation of the manual asymmetry with functional asymmetry of the EEG sensorimotor rhythm suggests that it is determined by the formation of the brain FMCR lateralization.     

Functional Differences between Keratins of Stratified and Simple Epithelia

Dividing populations of stratified and simple epithelial tissues express keratins 5 and 14, and keratins 8 and 18, respectively. It has been suggested that these keratins form a mechanical framework important to cellular integrity, since their absence gives rise to a blistering skin disorder in neonatal epidermis, and hemorrhaging within the embryonic liver. An unresolved fundamental issue is whether different keratins perform unique functions in epithelia. We now address this question using transgenic technology to express a K16-14 hybrid epidermal keratin transgene and a K18 simple epithelial keratin transgene in the epidermis of mice null for K14. Under conditions where the hybrid epidermal keratin restored a wild-type phenotype to newborn epidermis, K18 partially but not fully rescued. The explanation does not appear to reside in an inability of K18 to form 10-nm filaments with K5, which it does in vitro and in vivo. Rather, it appears that the keratin network formed between K5 and K18 is deficient in withstanding mechanical stress, leading to perturbations in the keratin network in regions of the skin that are subjected either to natural or to mechanically induced trauma. Taken together, these findings suggest that the loss of a type I epidermal keratin cannot be fully compensated by its counterpart of simple epithelial cells, and that in vivo, all keratins are not equivalent.     

Problems in the Integrated Study of Individual Differences

The properties of all the stages of evolution of matter, from the chemical to the sociohistorical, are part of man as well. In each of these properties, in addition to what is common and typical for groups of people, there is something that is unique to the individual and irreproducible. One characteristic noted in theoretical conceptions of individual differences is that they tend to study properties relating to different stages in the development of matter in isolation from one another. In most studies of differential psychophysiology, the biochemical and endocrine properties of the organism and the bioelectric properties of the nervous system are examined as if they had nothing to do with individual characteristics in the formation of classical Pavlovian conditioned reflexes. The psychological properties of the personality are examined in the Vygotsky and Leont'ev school independently of their relationship to somatic, neurophysiological, and psychodynamic properties (the properties of temperament).     

Similarities and Differences between Exome Sequences Found in a Variety of Tissues from the Same Individual

DNA is the most stable nucleic acid and most important store of genetic information. DNA sequences are conserved in virtually all the cells of a multicellular organism. To analyze the sequences of various individuals with distinct pathological disorders, DNA is routinely isolated from blood, independently of the tissue that is the target of the disease. This approach has proven useful for the identification of familial diseases where mutations are present in parental germinal cells. With the capacity to compare DNA sequences from distinct tissues or cells, present technology can be used to study whether DNA sequences in tissues are invariant. Here we explored the presence of specific SNVs (Single Nucleotide Variations) in various tissues of the same individual. We tested for the presence of tissue-specific exonic SNVs, taking blood exome as a control. We analyzed the chromosomal location of these SNVs. The number of SNVs per chromosome was found not to depend on chromosome length, but mainly on the number of protein-coding genes per chromosome. Although similar but not identical patterns of chromosomal distribution of tissue-specific SNVs were found, clear differences were detected. This observation supports the notion that each tissue has a specific SNV exome signature.     

On the Organization of Individual Differences in Sexual Behavior

SYNOPSIS. Research on the sexual differentiation of mating behaviorhas impeded progress in our understanding of the proximate basesof individual differences in two ways. First, by viewing variationas categorical rather than continuous, and second, by not placingsufficient emphasis on the fact that males and females differgenetically in many vertebrates, environmental contributionsto individual differences cannot be distinguished from geneticcontributions. Just as there are two levels of organizationof sex, so, too, are there two levels of organization of thesexual phenotype. Primary organization is the process of sexualdifferentiation that follows gonadal determination and is manifestas the morphological, physiological and behavioral aspects ofthe sexual phenotype. There is a second, and subsequent, levelof organization, however, that is directly related to primaryorganization and is the basis of individual variation in sexuallydimorphic behaviors. This level can be termed secondary organization.Because individual variation is the substance of evolutionarychange, understanding its organization will require both newparadigms and alternative animal model systems that allow separationof the effects of genes and hormones from environmental andexperiential stimuli. The plasticity of the sexual phenotypeand how each individual emerges from its own unique circumstancesintegrates these different levels of organization. As mightbe predicted, recent research suggests that the relationshipbetween primary and secondary organization and the developmentof individual differences in sociosexual behaviors involvesmore than just sex steroid hormones.     

Exploring Differences in the Content of Job Interviews between Youth with and without a Physical Disability

Objective

Although people with disabilities have great potential to provide advantages to work environments, many encounter barriers in finding employment, especially youth who are looking for their first job. A job interview is an essential component of obtaining employment. The objective of this study is to explore the content of the answers given in job interviews among youth with disabilities compared to typically developing youth.

Methods

A purposive sample of 31 youth (16 with typical development and 15 with disability) completed a mock job interview as part of an employment readiness study. The interview questions focused on skills and experiences, areas for improvement, and actions taken during problem-based scenarios. Transcribed interviews were analyzed using a content analysis of themes that emerged from the interviews.

Results

We found several similarities and differences between youth with disabilities and typically developing youth. Similarities included giving examples from school, emphasizing their “soft skills” (i.e., people and communication skills) and giving examples of relevant experience for the position. Both groups of youth gave similar examples for something they were proud of but fewer youth with disabilities provided examples. Differences in the content of job interview answers between the two groups included youth with disabilities: (1) disclosing their condition; (2) giving fewer examples related to customer service and teamwork skills; (3) experiencing greater challenges in providing feedback to team members and responding to scenario-based problem solving questions; and (4) drawing on examples from past work, volunteer and extra curricular activities.

Conclusions

Clinicians and educators should help youth to understand what their marketable skills are and how to highlight them in an interview. Employers need to understand that the experiences of youth with disabilities may be different than typically developing youth. Our findings also help to inform employment readiness programs by highlighting the areas where youth with disabilities may need extra help as compared to typically developing youth.     

不同功能型植物叶氮含量与光合特性的关系研究

在山西南部的霍山七里峪林场,确定乔木、灌木和草本物种共26个,用Li-3000A叶面积测定仪测量了叶面积的大小、用Li-6400便携式光合作用测定系统测定了叶光饱和速率（A_area）,计算了比叶重（LMA）、单位重量的光饱和光合速率（A_mass）、单位面积叶氮含量(Narea)、单位重量叶氮含量(N_mass)及光合氮利用效率(PNUE),研究了它们之间的不同和相互作用关系。结果表明：不同功能型植物的N_mass、A_area、A_mass、N_area和PNUE差异显著(p<0.05),植物叶片氮含量与植物光合生理特性具有显著相关关系,N_mass与A_area、A_mass和PNUE呈线性显著的正相关(p<0.05);N_area与A_area、A_mass、PNUE之间呈极显著的负相关(p<0.01)。     

Functional Differences between Mitochondrial Haplogroup T and Haplogroup H in HEK293 Cybrid Cells

Background

Epidemiological case-control studies have revealed associations between mitochondrial haplogroups and the onset and/or progression of various multifactorial diseases. For instance, mitochondrial haplogroup T was previously shown to be associated with vascular diseases, including coronary artery disease and diabetic retinopathy. In contrast, haplogroup H, the most frequent haplogroup in Europe, is often found to be more prevalent in healthy control subjects than in patient study groups. However, justifications for the assumption that haplogroups are functionally distinct are rare. Therefore, we attempted to compare differences in mitochondrial function between haplogroup H and T cybrids.

Methodology/Principal Findings

Mitochondrial haplogroup H and T cybrids were generated by fusion of HEK293 cells devoid of mitochondrial DNA with isolated thrombocytes of individuals with the respective haplogroups. These cybrid cells were analyzed for oxidative phosphorylation (OXPHOS) enzyme activities, mitochondrial DNA (mtDNA) copy number, growth rate and susceptibility to reactive oxygen species (ROS). We observed that haplogroup T cybrids have higher survival rate when challenged with hydrogen peroxide, indicating a higher capability to cope with oxidative stress.

Conclusions/Significance

The results of this study show that functional differences exist between HEK293 cybrid cells which differ in mitochondrial genomic background.     

Evidence for Intrinsic Differences in the Formation of Chromatin Domains in Drosophila Melanogaster

The results of an investigation into intrinsic differences in the formation of two different heterochromatic domains are presented. The study utilized two different position effect variegation mutants in Drosophila melanogaster for investigating the process of compacting different stretches of DNA into heterochromatin. Each stretch of DNA encodes for a gene that affects different aspects of bristle morphology. The expression of each gene is prevented when it is compacted into heterochromatin thus the genes serve as effective reporter systems to monitor the spread of heterochromatin. Both variegating mutants are scored in the same cell such that environmental and genetic background differences are unambiguously eliminated. Any differences observed in the repression of the two genes must therefore be the result of intrinsic differences in the heterochromatic compaction process for the two stretches of DNA. Studies of the effects different enhancers of variegation have upon the compaction of the two genes indicate each compaction event occurs independently of the other, and that different components are involved in the two processes. These results are discussed with regard to spreading heterochromatin and the role this process may play in regulating gene expression.     

异子蓬二型性种子的种皮结构及离子含量差异

异子蓬(Borszczowia aralocaspica)是中亚荒漠区系特有的一年生盐生植物,其种子具有二型性。通过检测异子蓬二型性种子中的生理生化物质以及观察种皮的结构,比较异子蓬二型性种子中营养物质、养分全量以及种皮结构的差异,结果表明:(1)异子蓬的棕色种子只有一层薄种皮,而黑色种子不但具有一层薄的内种皮还有一层坚硬致密的外种皮;(2)棕色种子的质量大、质量频数分布较为集中,并且吸水迅速,在吸水率较低时就能够大量萌发;(3)棕色种子的可溶性糖、可溶性蛋白质、全氮、全磷以及K+、Na+、K+/Na+和Mg2+/Na+都显著高于黑色种子。说明在繁殖子代、产生二型性种子时,异子蓬对棕色种子和黑色种子之间的繁殖投入存在着巨大的差异,这可能是导致异子蓬二型性种子产生差异性萌发机制的重要原因。     

Dopamine and the Creative Mind: Individual Differences in Creativity Are Predicted by Interactions between Dopamine Genes DAT and COMT

The dopaminergic (DA) system may be involved in creativity, however results of past studies are mixed. We attempted to clarify this putative relation by considering the mediofrontal and the nigrostriatal DA pathways, uniquely and in combination, and their contribution to two different measures of creativity–an abbreviated version of the Torrance Test of Creative Thinking, assessing divergent thinking, and a real-world creative achievement index. We found that creativity can be predicted from interactions between genetic polymorphisms related to frontal (COMT) and striatal (DAT) DA pathways. Importantly, the Torrance test and the real-world creative achievement index related to different genetic patterns, suggesting that these two measures tap into different aspects of creativity, and depend on distinct, but interacting, DA sub-systems. Specifically, we report that successful performance on the Torrance test is linked with dopaminergic polymorphisms associated with good cognitive flexibility and medium top-down control, or with weak cognitive flexibility and strong top-down control. The latter is particularly true for the originality factor of divergent thinking. High real-world creative achievement, on the other hand, as assessed by the Creative Achievement Questionnaire, is linked with dopaminergic polymorphisms associated with weak cognitive flexibility and weak top-down control. Taken altogether, our findings support the idea that human creativity relies on dopamine, and on the interaction between frontal and striatal dopaminergic pathways in particular. This interaction may help clarify some apparent inconsistencies in the prior literature, especially if the genes and/or creativity measures were analyzed separately.     

The Polarity of Lipid-Exposed Residues Contributes to the Functional Differences between Torpedo and Muscle-Type Nicotinic Receptors

A comparison between the Torpedo and muscle-type acetylcholine receptors (AChRs) reveals differences in several lipid-exposed amino acids, particularly in the polarity of those residues. The goal of this study was to characterize the role of eight lipid-exposed residues in the functional differences between the Torpedo and muscle-type AChRs. To this end, residues αS287, αC412, βY441, γM299, γS460, δM293, δS297 and δN305 in the Torpedo AChR were replaced with those found in the muscle-type receptor. Mutant receptor expression was measured in Xenopus oocytes using [¹²⁵I]-α-bungarotoxin, and AChR ion channel function was evaluated using the two-electrode voltage clamp. Eight mutant combinations resulted in an increase (1.5- to 5.2-fold) in AChR expression. Four mutant combinations produced a significant 46% decrease in the ACh 50% inhibitory concentration (EC₅₀), while three mutant combinations resulted in 1.7- to 2-fold increases in ACh EC₅₀. Finally, seven mutant combinations resulted in a decrease in normalized, ACh-induced currents. Our results suggest that these residues, although remote from the ion channel pore, (1) contribute to ion channel gating, (2) may affect trafficking of AChR into specialized membrane domains and (3) account for the functional differences between Torpedo and muscle-type AChR. These findings emphasize the importance of the lipid-protein interface in the functional differences between the Torpedo and muscle-type AChRs.     

Individual Differences in the Range of Sensory Modalities Experienced in Dreams.

The present study investigated the relationship between the recalled frequency of sensory modalities experienced in dreams and waking imagery abilities. Five hundred thirty-one undergraduate students completed 4 imagery ability tests and a dream recall questionnaire containing a question on the frequency of experience of the sensory modalities in dreams. A k-means cluster analysis of the Dream Sense Modality Scale indicated that the participants fell into 3 groups: the major modalities group, whose dreams were entirely visual, auditory, and kinesthetic; the all modalities group, who experienced all sense modalities in dreams; and the no modalities group, whose dreams were without sensory content. The participants' scores on the imagery tests in the 3 groups showed significant intergroup differences. The all modalities group showed the highest levels of ability in evoking vivid imagery and controlling visual imagery and the most frequent use of visual imagery compared with the other two groups. (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

Phylogenetic Differences in Content and Intensity of Periodic Proteins

Many proteins exhibit sequence periodicity, often correlated with a visible structural periodicity. The statistical significance of such periodicity can be assessed by means of a chi-squared-based test, with significance thresholds being calculated from shuffled sequences. Comparison of the complete proteomes of 45 species reveals striking differences in the proportion of periodic proteins and the intensity of the most significant periodicities. Eukaryotes tend to have a higher proportion of periodic proteins than eubacteria, which in turn tend to have more than archaea. The intensity of periodicity in the most periodic proteins is also greatest in eukaryotes. By contrast, the relatively small group of periodic proteins in archaea also tend to be weakly periodic compared to those of eukaryotes and eubacteria. Exceptions to this general rule are found in those prokaryotes with multicellular life-cycle phases, e.g., Methanosarcina sp., or Anabaena sp., which have more periodicities than prokaryotes in general, and in unicellular eukaryotes, which have fewer than multicellular eukaryotes. The distribution of significantly periodic proteins in eukaryotes is over a wide range of period lengths, whereas prokaryotic proteins typically have a more limited set of period lengths. This is further investigated by repeating the analysis on the NRL-3D database of proteins of solved structure. Some short-range periodicities are explicable in terms of basic secondary structure, e.g., alpha helices, while middle-range periodicities are frequently found to consist of known short Pfam domains, e.g., leucine-rich repeats, tetratricopeptides or armadillo domains. However, not all can be explained in this way.Reviewing Editor: Dr. John Oakeshott     

Representing Representation: Integration between the Temporal Lobe and the Posterior Cingulate Influences the Content and Form of Spontaneous Thought

When not engaged in the moment, we often spontaneously represent people, places and events that are not present in the environment. Although this capacity has been linked to the default mode network (DMN), it remains unclear how interactions between the nodes of this network give rise to particular mental experiences during spontaneous thought. One hypothesis is that the core of the DMN integrates information from medial and lateral temporal lobe memory systems, which represent different aspects of knowledge. Individual differences in the connectivity between temporal lobe regions and the default mode network core would then predict differences in the content and form of people’s spontaneous thoughts. This study tested this hypothesis by examining the relationship between seed-based functional connectivity and the contents of spontaneous thought recorded in a laboratory study several days later. Variations in connectivity from both medial and lateral temporal lobe regions was associated with different patterns of spontaneous thought and these effects converged on an overlapping region in the posterior cingulate cortex. We propose that the posterior core of the DMN acts as a representational hub that integrates information represented in medial and lateral temporal lobe and this process is important in determining the content and form of spontaneous thought.     

Lymphocyte Sensitization in Asthma with Special Reference to Nature and Identity of Intrinsic Form

Studies of lymphocyte sensitization in patients with asthma showed that the intrinsic and extrinsic forms of the disease fell into two distinct groups. Intrinsic disease showed a general sensitization to a number of non-specific antigens, while the extrinsic form had only slight elevation above normal values. These findings suggest that intrinsic asthma results from a defect of general immunity, whereas extrinsic asthma is a specific sensitization.