Transcriptomic analyses support the similarity of gene expression between brain and testis in human as well as mouse.

Abstract:

:We previously revealed similarity in gene expression patterns between human brain and testis, based on digital differential display analyses of 760 human Unigenes. In the present work, we reanalyzed the gene expression data in many tissues of human and mouse for a large number of genes almost covering the respective whole genomes. The results indicated that both in human and in mouse, the gene expression profiles exhibited by brain, cerebellum and testis are most similar to each other compared with other tissues.

journal_name

Cytogenet Genome Res

authors

Guo JH,Huang Q,Studholme DJ,Wu CQ,Zhao Z

doi

10.1159/000086378

keywords:

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

107-9

issue

2

eissn

1424-8581

issn

1424-859X

pii

86378

journal_volume

111

pub_type

杂志文章
  • HIV-1/AIDS susceptibility and copy number variation in CCL3L1, a gene encoding a natural ligand for HIV-1 co-receptor CCR5.

    abstract::Variations of gene copy number in the human genome are increasingly recognized as a genetic factor in phenotypic variation. Human CC chemokine ligand 3-like 1 gene (CCL3L1), which is located on human chromosome 17q11.2, is highly variable in copy number owing to having a hot spot for segmental duplications. CCL3L1, a ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000184703

    authors: Nakajima T,Kaur G,Mehra N,Kimura A

    更新日期:2008-01-01 00:00:00

  • Elevated chromosome translocation frequencies in New Zealand nuclear test veterans.

    abstract::In 1957/58 the British Government conducted a series of nuclear tests in the mid-Pacific codenamed Operation Grapple, which involved several naval vessels from Britain and New Zealand. Two New Zealand frigates with 551 personnel onboard were stationed at various distances between 20 and 150 nautical miles from ground ...

    journal_title:Cytogenetic and genome research

    pub_type: 历史文章,杂志文章

    doi:10.1159/000125832

    authors: Wahab MA,Nickless EM,Najar-M'kacher R,Parmentier C,Podd JV,Rowland RE

    更新日期:2008-01-01 00:00:00

  • Molecular cytogenetics in the study of cutaneous T-cell lymphomas (CTCL).

    abstract::The etiology of primary cutaneous T-cell lymphomas (CTCL) has been poorly understood. CTCL patients show a large variety of non-clonal and clonal chromosome aberrations, but no specific aberration has been found until recently. This review describes cytogenetic and molecular cytogenetic findings and their relevance to...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000108320

    authors: Karenko L,Hahtola S,Ranki A

    更新日期:2007-01-01 00:00:00

  • Pesticides and the induction of aneuploidy in human sperm.

    abstract::Pesticides are some of the most frequently released toxic chemicals into the environment. Exposure to them has been associated with reproductive dysfunction, but the knowledge of the genotoxic risks of these substances is still limited. In vitro and in vivo, many pesticides are shown to induce aneuploidy. Analysis of ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000086915

    authors: Härkönen K

    更新日期:2005-01-01 00:00:00

  • Chromosomal mechanisms underlying the karyotype evolution of the oriental voles (Muridae, Eothenomys).

    abstract::We have investigated the karyotype relationships of two oriental voles, i.e. the Yulong vole (Eothenomys proditor, 2n = 32) and the large oriental vole (Eothenomys miletus, 2n = 56) as well as the Clarke's vole (Microtus clarkei, 2n = 52), by a combined approach of cross-species chromosome painting and high-resolution...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000091928

    authors: Li T,Wang J,Su W,Yang F

    更新日期:2006-01-01 00:00:00

  • A model for genetic complementation controlling the chromosomal abnormalities and loss of heterozygosity formation in cancer.

    abstract::The relationship between the apparently random chromosomal changes found in aneuploidy and the genetic instability driving the progression of cancer is not clear. We report a test of the hypothesis that aneuploid chromosomal abnormalities might be selected to preserve cell-survival genes during loss of heterozygosity ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000100406

    authors: Nestor AL,Hollopeter SL,Matsui SI,Allison D

    更新日期:2007-01-01 00:00:00

  • A preliminary genetic map in Solea senegalensis (Pleuronectiformes, Soleidae) using BAC-FISH and next-generation sequencing.

    abstract::This article presents the first physical mapping carried out in the Senegalese sole (Solea senegalensis), an important marine fish species of Southern Europe. Eight probes were designated to pick up genes of interest in aquaculture (candidate genes) from a bacterial artificial chromosome (BAC) library using a method o...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000355001

    authors: García-Cegarra A,Merlo MA,Ponce M,Portela-Bens S,Cross I,Manchado M,Rebordinos L

    更新日期:2013-01-01 00:00:00

  • Classical and Molecular Cytogenetics of the Panther Genet Genetta maculata (Mammalia, Carnivora, Viverridae).

    abstract::Genets (Genetta) are a genus of African mammalian carnivorans with 14 currently recognized species, although taxonomic uncertainties remain, particularly regarding the number of species within the large-spotted genet complex. This study presents the first banded karyotype and molecular cytogenetic analysis of a geneti...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000450627

    authors: Matoso Silva R,Adega F,Kjöllerström HJ,Labuschagne K,Kotze A,Fernandes C,Chaves R,do Mar Oom M

    更新日期:2016-01-01 00:00:00

  • The centromeric satellite of the wedge sole (Dicologoglossa cuneata, Pleuronectiformes) is composed mainly of a sequence motif conserved in other vertebrate centromeric DNAs.

    abstract::Here, a new satellite-DNA family is isolated and characterized from wedge sole, Dicologoglossa cuneata Moreau, 1881 (Pleuronectiformes), a fish having a small genome. This satellite-DNA family of sequences was isolated by conventional cloning after digestion of genomic DNA with the DraI restriction enzyme. Repeat unit...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000138896

    authors: de la Herrán R,Robles F,Navas JI,López-Flores I,Herrera M,Hachero I,Garrido-Ramos MA,Ruiz Rejón C,Ruiz Rejón M

    更新日期:2008-01-01 00:00:00

  • Chromosomal Rearrangements during Turtle Evolution Altered the Synteny of Genes Involved in Vertebrate Sex Determination.

    abstract::Sex-determining mechanisms (SDMs) set an individual's sexual fate by its genotype (genotypic sex determination, GSD) or environmental factors like temperature (temperature- dependent sex determination, TSD), as in turtles where the GSD "trigger" remains unknown. SDMs co-evolve with turtle chromosome number, perhaps be...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000497302

    authors: Lee L,Montiel EE,Navarro-Domínguez BM,Valenzuela N

    更新日期:2019-01-01 00:00:00

  • Cloning, expression, and chromosomal localization of the mouse gene (Scgb3a1, alias Ugrp2) that encodes a member of the novel uteroglobin-related protein gene family.

    abstract::The mouse UGRP gene family consists of two genes, Ugrp1 and Ugrp2. In this study, the genomic structure and expression patterns of Ugrp2 and its alternative spliced form were characterized. The authentic Ugrp2 gene has three exons and two introns, similar to the Ugrp1 gene, which produces a secreted protein. The Ugrp2...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000064067

    authors: Niimi T,Copeland NG,Gilbert DJ,Jenkins NA,Srisodsai A,Zimonjic DB,Keck-Waggoner CL,Popescu NC,Kimura S

    更新日期:2002-01-01 00:00:00

  • Comparative mapping in equids: the asine X chromosome is rearranged compared to horse and Hartmann's mountain zebra.

    abstract::The X chromosomes of the extant equids, in general, share morphology and banding pattern similarities. However, the donkey X is, in part, an exception because of significantly different centromeric index and variant banding patterns in the pericentromeric region. To verify the underlying molecular basis of this differ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000063050

    authors: Raudsepp T,Lear TL,Chowdhary BP

    更新日期:2002-01-01 00:00:00

  • Cytogenetic Insights into the Evolution of Chromosomes and Sex Determination Reveal Striking Homology of Turtle Sex Chromosomes to Amphibian Autosomes.

    abstract::Turtle karyotypes are highly conserved compared to other vertebrates; yet, variation in diploid number (2n = 26-68) reflects profound genomic reorganization, which correlates with evolutionary turnovers in sex determination. We evaluate the published literature and newly collected comparative cytogenetic data (G- and ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000447478

    authors: Montiel EE,Badenhorst D,Lee LS,Literman R,Trifonov V,Valenzuela N

    更新日期:2016-01-01 00:00:00

  • Evolutionary molecular cytogenetics of catarrhine primates: past, present and future.

    abstract::The catarrhine primates were the first group of species studied with comparative molecular cytogenetics. Many of the fundamental techniques and principles of analysis were initially applied to comparisons in these primates, including interspecific chromosome painting, reciprocal chromosome painting and the extensive u...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000339381

    authors: Stanyon R,Rocchi M,Bigoni F,Archidiacono N

    更新日期:2012-01-01 00:00:00

  • Long dsRNA and silent genes strike back:RNAi in mouse oocytes and early embryos.

    abstract::RNA interference (RNAi) refers to the selective degradation of mRNA induced by double-stranded RNA (dsRNA), first discovered in Caenorhabditis elegans. Homology-dependent silencing phenomena related to RNAi have been observed in many species from all eukaryotic kingdoms. RNAi and related mechanisms share several conse...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000078215

    authors: Svoboda P

    更新日期:2004-01-01 00:00:00

  • Oligonucleotide array comparative genomic hybridization refines the structure of 8p23.1, 17q12 and 20q13.2 amplifications in gastric carcinomas.

    abstract::Oligonucleotide array comparative genomic hybridization (aCGH) was applied on fifteen gastric cancer (GCA) samples to reveal information of DNA copy number changes at an exon-level resolution. Twelve of the samples represented the intestinal (IGCA) and three the diffuse (DGCA) type of GCA. The samples had previously b...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000109617

    authors: Vauhkonen H,Vauhkonen M,Sipponen P,Knuutila S

    更新日期:2007-01-01 00:00:00

  • Mismatch repair proteins: key regulators of genetic recombination.

    abstract::Mismatch repair (MMR) systems are central to maintaining genome stability in prokaryotes and eukaryotes. MMR proteins play a fundamental role in avoiding mutations, primarily by removing misincorporation errors that occur during DNA replication. MMR proteins also act during genetic recombination in steps that include ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000080593

    authors: Surtees JA,Argueso JL,Alani E

    更新日期:2004-01-01 00:00:00

  • Why is SCA12 different from other SCAs?

    abstract::Spinocerebellar ataxia type 12 (SCA12), now described in European-American and Asian (Indian) pedigrees, is unique among the SCAs from clinical, pathological, and molecular perspectives. Clinically, the distinguishing feature is early and prominent action tremor with variability in other signs. Pathologically, brain M...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章,评审

    doi:10.1159/000072854

    authors: Holmes SE,O'Hearn E,Margolis RL

    更新日期:2003-01-01 00:00:00

  • Fragile sites in domestic animal chromosomes: molecular insights and challenges.

    abstract::Fragile sites are intriguing cytogenetic phenomena that have been extensively investigated in human and laboratory animal chromosomes over the past 40 years, but domestic animal species have been studied sporadically. Interest in the field has been recently renewed as increasing numbers of fragile site regions are clo...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000245910

    authors: Riggs PK,Rønne M

    更新日期:2009-01-01 00:00:00

  • The Hypermethylated Regions in Avian Chromosomes.

    abstract::Chromosomal locations and amounts of 5-methylcytosine-rich chromosome regions were detected in the karyotypes of 13 bird species by indirect immunofluorescence using a monoclonal anti-5-methylcytosine antibody. These species belong to 7 orders and 10 families of modern (Neognathae) and primitive (Palaeognathae) birds ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000464268

    authors: Schmid M,Steinlein C

    更新日期:2017-01-01 00:00:00

  • Chromosome evolution in the lizard genus Gekko (Gekkonidae, Squamata, Reptilia) in the East Asian islands.

    abstract::The lizard genus Gekko consists of over 30 species distributed in Asia and Oceania. From the insular region of East Asia including Japan and Taiwan, 9 species (G. hokouensis, G. japonicus, G. shibatai, G. tawaensis, G. vertebralis,G. yakuensis, and 3 undescribed species) are currently recognized. We made karyological ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000303334

    authors: Shibaike Y,Takahashi Y,Arikura I,Iiizumi R,Kitakawa S,Sakai M,Imaoka C,Shiro H,Tanaka H,Akakubo N,Nakano M,Watanabe M,Ohne K,Kubota S,Kohno S,Ota H

    更新日期:2009-01-01 00:00:00

  • Equine FISH mapping of 36 genes known to locate on human chromosome ends.

    abstract::The INRA and the CHORI-241 horse BAC libraries were screened by hybridization with DNA probes and/or directly by PCR with primers designed in consensus sequences of genes localized at the end of each human chromosome. BAC clones were retrieved and 36 could be FISH mapped after the expected gene was confirmed in each B...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000085669

    authors: Perrocheau M,Boutreux V,Chadi-Taourit S,Di Meo GP,Perucatti A,Incarnato D,Cribiu EP,Guérin G,Iannuzzi L

    更新日期:2005-01-01 00:00:00

  • A Small Supernumerary Marker Derived from the Pericentromeric Region of Chromosome 5: Case Report and Delineation of Partial Trisomy 5p Phenotype.

    abstract::A 17-year-old girl presented with a distinct phenotype mainly featuring craniofacial dysmorphism, including a disproportioned large, round, elongated face; hypertelorism; deep-set eyes with short palpebral fissures; obesity (BMI 37), and a neuropsychiatric disorder with high-functioning autism. Postnatal conventional ...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000481331

    authors: Camerota L,Pitzianti M,Postorivo D,Nardone AM,Ligas C,Moretti C,Pasini A,Brancati F

    更新日期:2017-01-01 00:00:00

  • Chromosome studies of European cyprinid fishes: cross-species painting reveals natural allotetraploid origin of a Carassius female with 206 chromosomes.

    abstract::A single female with 206 chromosomes and another 26 females with 156 chromosomes identified as Prussian carp, Carassius gibelio, and 5 individuals with 100 chromosomes identified as crucian carp, C. carassius, were sampled during field survey in one locality in the upper Elbe River. To identify the origin of females w...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000350689

    authors: Knytl M,Kalous L,Symonová R,Rylková K,Ráb P

    更新日期:2013-01-01 00:00:00

  • Mechanisms of nondisjunction in human spermatogenesis.

    abstract::A reduction in recombination in the pseudoautosomal region is associated with an increased frequency of aneuploid 24,XY human sperm. Similarly, individuals with paternally derived Klinefelter syndrome (47,XXY) also have a paucity of recombination in the chromosomes that have undergone nondisjunction. Meiotic studies u...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000086895

    authors: Martin RH

    更新日期:2005-01-01 00:00:00

  • How common are common fragile sites in humans: interindividual variation in the distribution of aphidicolin-induced fragile sites.

    abstract::To obtain an estimate of the variation in common fragile sites (CFSs) among individuals, aphidicolin (APC)-induced chromosomal breakage data were analyzed for 20 karyotypically normal adult humans. As it is specifically designed to meet the analytical requirements for considering fragile sites as presence/absence char...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000073411

    authors: Denison SR,Simper RK,Greenbaum IF

    更新日期:2003-01-01 00:00:00

  • Evolution of Bird Sex Chromosomes Narrated by Repetitive Sequences: Unusual W Chromosome Enlargement in Gallinula melanops (Aves: Gruiformes: Rallidae).

    abstract::Among birds, species with the ZZ/ZW sex determination system generally show significant differences in morphology and size between the Z and W chromosomes (with the W usually being smaller than the Z). In the present study, we report for the first time the karyotype of the spot-flanked gallinule (Gallinula melanops) b...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000501381

    authors: Gunski RJ,Kretschmer R,Santos de Souza M,de Oliveira Furo I,Barcellos SA,Costa AL,Cioffi MB,de Oliveira EHC,Del Valle Garnero A

    更新日期:2019-01-01 00:00:00

  • A high density of human communication-associated genes in chromosome 7q31-q36: differential expression in human and non-human primate cortices.

    abstract::The human brain is distinguished by its remarkable size, high energy consumption, and cognitive abilities compared to all other mammals and non-human primates. However, little is known about what has accelerated brain evolution in the human lineage. One possible explanation is that the appearance of advanced communica...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000335465

    authors: Schneider E,Jensen LR,Farcas R,Kondova I,Bontrop RE,Navarro B,Fuchs E,Kuss AW,Haaf T

    更新日期:2012-01-01 00:00:00

  • The controversial telomeres of lily plants.

    abstract::The molecular structure of the exceptional telomeres of six plant species belonging to the order Asparagales and two species of the order Liliales was analyzed using Southern blot and fluorescence in situ hybridization. Three different situations were found, namely: i) In the two Liliales species, Tulipa australis (Li...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000082393

    authors: de la Herrán R,Cuñado N,Navajas-Pérez R,Santos JL,Ruiz Rejón C,Garrido-Ramos MA,Ruiz Rejón M

    更新日期:2005-01-01 00:00:00

  • Condensation of rye chromatin in somatic interphase nuclei of Ph1 and ph1b wheat.

    abstract::The Ph1 locus in hexaploid wheat (Triticum aestivum L.) enforces diploid-like behavior in the first metaphase of meiosis. To test the hypothesis that this chromosome pairing control is exercised by affecting the degree of chromatin condensation, the dispersion of rye chromatin in interphase nuclei in somatic tissues o...

    journal_title:Cytogenetic and genome research

    pub_type: 杂志文章

    doi:10.1159/000112072

    authors: Kopecky D,Allen DC,Duchoslav M,Dolezel J,Lukaszewski AJ

    更新日期:2007-01-01 00:00:00