浙江大学学报(农业与生命科学版)
浙江大學學報(農業與生命科學版)
절강대학학보(농업여생명과학판)
JOURNAL OF ZHEJIANG UNIVERSITY(AGRICULTURE & LIFE SCIENCES)
2015年
4期
394-406
,共13页
鲍林飞%王新星%何健瑜%范美华%高鹏%廖智
鮑林飛%王新星%何健瑜%範美華%高鵬%廖智
포림비%왕신성%하건유%범미화%고붕%료지
厚壳贻贝%外套膜%贝壳基质蛋白%转录组
厚殼貽貝%外套膜%貝殼基質蛋白%轉錄組
후각이패%외투막%패각기질단백%전록조
Mytilus coruscus%mantle%shell matrix protein%transcriptome
为了解贻贝贝壳基质蛋白的分子多样性,采用Illumina高通量测序平台,对厚壳贻贝( Mytilus coruscus)外套膜组织开展转录组文库构建及从头测序研究,总计产出6970102920 nt数据,共77445588条干净阅读子;经序列拼接与组装,获得厚壳贻贝外套膜转录组单一基因共计106452个,总长55222289 nt ,平均长度519 nt ,N50达到754 nt ;并对上述单一基因进行了生物学功能注释和聚类分析。为进一步挖掘贻贝贝壳基质蛋白相关基因,通过对单一基因的序列注释以及利用已知贝壳基质蛋白序列进行本地搜索,共鉴定出与12种已知贝壳基质蛋白同源的厚壳贻贝外套膜单一基因124条。通过对厚壳贻贝贝壳基质蛋白单一基因进行序列分析和比较,发现厚壳贻贝与其他软体动物,如鲍属、牡蛎属和珠母贝属等在贝壳基质蛋白组成以及序列上具有一定的保守性,暗示着贝壳基质蛋白可能具有共同的起源;同时,首次从贻贝属中发现了3种贝壳棱柱层特异的贝壳基质蛋白单一基因。这为后续贻贝贝壳基质蛋白的大规模鉴定以及对贝壳形成机制的探讨奠定了基础。
為瞭解貽貝貝殼基質蛋白的分子多樣性,採用Illumina高通量測序平檯,對厚殼貽貝( Mytilus coruscus)外套膜組織開展轉錄組文庫構建及從頭測序研究,總計產齣6970102920 nt數據,共77445588條榦淨閱讀子;經序列拼接與組裝,穫得厚殼貽貝外套膜轉錄組單一基因共計106452箇,總長55222289 nt ,平均長度519 nt ,N50達到754 nt ;併對上述單一基因進行瞭生物學功能註釋和聚類分析。為進一步挖掘貽貝貝殼基質蛋白相關基因,通過對單一基因的序列註釋以及利用已知貝殼基質蛋白序列進行本地搜索,共鑒定齣與12種已知貝殼基質蛋白同源的厚殼貽貝外套膜單一基因124條。通過對厚殼貽貝貝殼基質蛋白單一基因進行序列分析和比較,髮現厚殼貽貝與其他軟體動物,如鮑屬、牡蠣屬和珠母貝屬等在貝殼基質蛋白組成以及序列上具有一定的保守性,暗示著貝殼基質蛋白可能具有共同的起源;同時,首次從貽貝屬中髮現瞭3種貝殼稜柱層特異的貝殼基質蛋白單一基因。這為後續貽貝貝殼基質蛋白的大規模鑒定以及對貝殼形成機製的探討奠定瞭基礎。
위료해이패패각기질단백적분자다양성,채용Illumina고통량측서평태,대후각이패( Mytilus coruscus)외투막조직개전전록조문고구건급종두측서연구,총계산출6970102920 nt수거,공77445588조간정열독자;경서렬병접여조장,획득후각이패외투막전록조단일기인공계106452개,총장55222289 nt ,평균장도519 nt ,N50체도754 nt ;병대상술단일기인진행료생물학공능주석화취류분석。위진일보알굴이패패각기질단백상관기인,통과대단일기인적서렬주석이급이용이지패각기질단백서렬진행본지수색,공감정출여12충이지패각기질단백동원적후각이패외투막단일기인124조。통과대후각이패패각기질단백단일기인진행서렬분석화비교,발현후각이패여기타연체동물,여포속、모려속화주모패속등재패각기질단백조성이급서렬상구유일정적보수성,암시착패각기질단백가능구유공동적기원;동시,수차종이패속중발현료3충패각릉주층특이적패각기질단백단일기인。저위후속이패패각기질단백적대규모감정이급대패각형성궤제적탐토전정료기출。
Summary Mollusk shell is an exoskeleton made up of organic mineral particles and its function is to protect the inner soft body from predators and environmental damage . Due to its superior mechanical properties , such as stiffness , fracture toughness , and tensile strength , the mollusk shell has been investigated as an excellent biomaterial and as bio‐mineralization model over the past decades . Previous studies have revealed that mollusk shell was consist of a mineral phase ( calcium carbonate) and an organic matrix ( proteins , polysaccharides and lipids) . The organic matrix intercalated in a shell is generally assumed to play an important role in crystal nucleation , crystal orientation , crystal size regulation , and crystal polymorphism and contributing to the shell?s mechanical properties . Recent advances on ease and availability of high throughput RNA‐sequencing have resulted in a sharp increase in transcriptome data for invertebrate bio‐minerals . However , for Mytilus , bio‐mineralization mechanisms and shell formation were restricted to obtain by deficiency of transcriptome information .
<br> To understand the molecular diversity of matrix proteins from mussel shell and to develop a transcriptome from the adult mantle tissue of M . coruscus , the transcriptome sequencing of M . coruscus mantle was performed by Illumina platform . A total of 77 445 588 paired‐end reads amounting to 6 Gb of sequence data were generated and further assembled de novo with Trinity software . A transcriptome was produced after filtering and quality checking , yielded a final set of 106 425 high quality mantle unigenes for analysis . To obtain an integrated view of the transcriptional events of bio‐mineralization related processes in M . coruscus mantle , the unique transcript library was screened for reported shell matrix proteins ( SMPs) . Taken together , 124 unigenes were identified with significant hits ( E‐value < 10-5 ) to 12 reported bio‐mineralization related proteins including all known Mytilus SMPs . The most abundant unigenes out of 124 matched ones were annotated as calponin , followed by fibronectin , perlucin , nacrein , and Shematrin . Most of homologues were from Crassostrea , Pinctada , H aliotis , and Mytilus , which showed that M . coruscus mantle unigene encoded putative proteins exhibiting sequence similarities with previously characterized SMPs of other Bivalvias , indicating a common originate for these SMPs .
<br> In conclusion , a comprehensive transcriptomic resource for the Mytilus SMPs was presented in this paper , providing insight into the protein composition of the shell . The transcriptomic resource can also provide a foundation for further investigations on the formation and bio‐mineralization of mussel shell .