17 Resultado que arroja la guía de información
17.2 Análisis de encuestas de graficas de barras
As of March 1, 2012, there were only 252,832
Arachis ESTs in NCBI’s GenBank, 178,490
from A. hypogaea (Feng et al.2012). Extensive
sequencing of expressed genes has occurred over the last 4 years as costs for next-generation sequencing have dropped precipitously. Much of this sequence has been deposited in public
databases along with previously generated
microarray data (Table6.3). Analyses of differ-
ential gene expression and pathways across developmental series and in response to pests, diseases, and abiotic stress have been the primary objectives across these studies. Several microar-
ray experiments preceded high-throughput
sequencing and were informative for the study of drought stress response. Expressed sequence from all primary organs of cultivated peanut is available and can be used to construct gene networks that will inform the study of traits that
impact productivity (Clevenger et al.2016). For
example, an oil metabolic network of peanut and three other oilseed crops (soybean, rapeseed, and sesame) has been constructed using available
EST data and is accessible at http://ocri-
genomics.org/ocsESTdb (Ke et al. 2015). Knowledge of gene expression, association of expressed genes with gene models in the newly released diploid Arachis genomes (Bertioli et al.
2016), and putative positions with respect to
QTL are contributing to hypothesis development and testing of gene function.
Testing of gene function often includes quantitative analysis of expression patterns across time, developmental stages, treatments, etc. Such analyses require a frame of reference. i.e., genes whose expression is relatively uniform regardless of tissue or treatment. Four studies to identify suitable reference genes for peanut have
been conducted, testing 8–14 candidates across a
variety of tissues (Table 6.4). Both alcohol
dehydrogenase III and alpha tubulin showed high stability and moderate abundance in more than one study.
In addition to extensive transcriptome data, proteome data are being produced to further evaluate gene function, study physiological responses, and develop proteome maps. While a couple of studies have been focused on the peanut leaf proteome, with or without stress
(Kottapalli et al.2009; Katam et al.2010), most
have targeted peanut gynophores (Li et al. 2013;
Sun et al. 2013; Xia et al. 2015, Zhao et al.
2015b), organs that are relatively unique among crop plants but whose response to gravity is critical for reproductive success. In addition to being transcribed, most genes must be translated to perform a function, and the coordination of transcription and translation can be different for different genes depending on the regulation of expression and turnover rates. Analyzing the proteome independently and in concert with the transcriptome can provide new insight into gene
action. For example, Zhao et al. (2015b) only
identified transcripts for 38 out of 69 key peg
proteins while transcripts were not identified for
some abundant proteins and vice versa.
6.4
Bioinformatics Resources
Bioinformatics resources for peanut at the time of writing include the genome sequences of the diploid progenitors of cultivated peanut, A. dura- nensis and A. ipaensis, as well as extensive tran- scriptome sequences for wild diploid accessions
and for cultivated peanut (Bertioli et al.2016). The
Table 6.3 Publicly available gene expression data sets
Data type NCBI accession Publication Target
tissues
Treatment/ Experimental materialsa
Objective
RNAseq PRJNA312741 Qingdao Agric Univ, unpubl. Leaf Salinity stress
RNAseq PRJNA298453 Shandong Acad Agric Sci, unpubl. Gynophore Light and dark
RNAseq PRJNA291488 Bertioli et al. (2016) 22 Developmental
stages
Also accessible at peanutbase. org
RNAseq PRJNA290039 Zhao et al. (2015b) Gynophore Developmental
stages
Integrated with proteome analysis
RNAseq PRJNA286040 Peng et al. (2016) Leaf Two genotypes SSR discovery
RNAseq PRJNA284674 Guimaraes et al. (2015) Root A. stenosperma/
nematode
Pest pressure time course
RNAseq PRJNA251584 Fujian Agric For Univ, unpubl. 8 Biotic and abiotic
stress
miRNAseq PRJNA251517 Zhao et al. (2015a) Root Organ
RNAseq PRJNA248910 Chopra et al. (2014) Leaf, pod,
root A. hypogaea A. ipaensis A. duranensis Assembler comparisons
RNAseq PRJNA243319 Li et al. (2014) Leaf, root,
stem
Water deficit and ABA
Differential gene expression
RNAseq PRJNA233534 Geng et al. (2014) Leaf, stem,
pod, root
One genotype Tissue-specific
gene discovery
RNAseq SRA053198 Chen et al. (2013) Pod Above and below
ground
Early embryo abortion
RNAseq PRJNA185732 Yin et al. (2013) Seed Two genotypes Oil metabolism
RNAseq PRJNA181974 Xia et al. (2013), Zhong et al.(2016) Gynophore Developmental
stages/light–dark Differential gene expression SSR discovery Small RNAseq
PRJNA146213 Zhai et al. (2011) Flower,
nodule
Organs Legume
conservation
Microarray PRJNA143823 Chen et al. (2012) Leaves,
pods
Five varieties Expression in
response to selection
Microarray PRJNA138261 Guo et al. (2011) Seeds Two cultivars,
Aspergillus infected Differential response to Aspergillus exposure Microarray PRJNA123433, PRJNA123473, PRJNA119623
Payton, unpubl. Leaf Two genotypes,
Heat stress
Comparison of acclimated and unacclimated response
Microarray PRJNA106585 Payton et al. (2009) Leaf, stem,
peg, pod, root
Organs Tissue-specific
gene expression
RNAseq PRJNA78245 Guimaraes et al. (2012) Leaf A. stenosperma/
leaf spot
Infection time course
GenBank (A. duranensis: GCA_000817695.1, A. ipaensis: GCA_000816755.1). Efforts are under- way to sequence the tetraploid peanut genome, along with extensive high-density genotyping of diverse tetraploid accessions and RIL (Recombi- nant Inbred Lines) populations.
The primary repository for peanut genetic and
genomic data for the IPGI is PeanutBase (http://
peanutbase.org), which holds genome sequences, gene model sequences and annotations, genetic maps, mapped traits (QTL), expression data, germplasm information, and a variety of tools for browsing, searching, querying, and interrelating
these data sets. These tools are briefly described
below.