Scientia Agricultura Sinica ›› 2021, Vol. 54 ›› Issue (9): 2027-2038.doi: 10.3864/j.issn.0578-1752.2021.09.018

• ANIMAL SCIENCE·VETERINARY SCIENCE·RESOURCE INSECT • Previous Articles    

Expression Analysis of IGF1-PI3K-Akt-Dependent Pathway Genes in Skeletal Muscle and Liver Tissue of Yellow Feather Broilers

SHU JingTing1(),JI GaiGe1,SHAN YanJu1,ZHANG Ming1,JU XiaoJun1,LIU YiFan1,TU YunJie1,SHENG ZhongWei1,TANG YanFei2,JIANG HuaLian2,ZOU JianMin1()   

  1. 1Jiangsu Institute of Poultry Science/Key laboratory for Poultry Genetics and Breeding of Jiangsu Province, Yangzhou 225125, Jiangsu
    2Guangxi Fufeng Farm Group Co., Ltd., Nanning 530024
  • Received:2020-07-28 Accepted:2020-10-16 Online:2021-05-01 Published:2021-05-10
  • Contact: JianMin ZOU E-mail:shujingting@163.com;jqszjm@163.com

Abstract:

【Objective】IGF1-PI3K-Akt signal pathway have been implicated in the regulation of growth and development of chicken. In the present study, the expression of IGF, IGF1R and IRS1genes of IGF1-PI3K-Akt signal pathway was first studied in skeletal muscle and liver tissues of Guangxi partridge chickens with slow growth rate and Huashan partridge chickens with moderate growth rate, which would provide a reference for clarifying the regulation mechanism of growth and development of yellow feather broilers. 【Method】SPSS20.0 software was used to compare the differences of growth traits between Guangxi partridge chickens and Huashan partridge chickens. Expression of IGF1, IGF1R and IRS1 was quantified by RT-PCR in the breast muscle (BM), leg muscle (LM) and liver on days 9, 12, and 16 of embryonic development, as well as at 0, 7, 21, 35, 49, and 63 days post-hatching (PH) in the two chicken breeds, and the correlations between the gene expression level and body weight as well as tissue weight were also analyzed by SPSS20.0 software. 【Result】The body weight, skeletal muscle and liver weight of chicken in the early growth development showed significant breed- and age-specificity. The growth of Huashan partridge chickens had far exceeded that of Guangxi partridge chickens from the late embryonic development. The expression patterns of IGF1, IGF1R and IRS1 showed significant differences in breed-, tissue- and age-specific fashion. Overall, the expression levels of the three genes in skeletal muscles of embryonic development were much higher than those in liver; in contrast, the expression levels in liver were higher than those in skeletal muscle at post-hatching development. As for breed, expression levels of the studied genes in skeletal muscle of Guangxi partridge chickens were higher than those in Huashan partridge chickens; in contrast, liver expression levels were higher in Huashan partridge chickens. IGF1 mRNA could be detected as early as on E9 d in the skeletal muscles of both chicken breeds, and the highest level was appeared at this stage in LM, significantly higher than those on the other studied development stages expect on E12 d, and the lowest level was appeared on 0 d at hatching; while in BM, the highest level was appeared on E12 d and lowest level was appeared on 63 d; however, the level of IGF1 mRNA differed between breeds in liver. For Guangxi partridge chickens, the highest level was observed on 21 d and there was no expression during embryonic development, whereas the highest level was found on 49 d and very low level during embryonic development in Huashan partridge chickens. IGF1R mRNA could be detected at the whole studied stages in skeletal muscles and liver of both chicken breeds, and the highest level was appeared on E9 d in both BM and LM, significantly higher than those on the other studied development stages in Guangxi partridge chickens, and significantly higher than those on the other studied development stages expect on E12 d in Huashan partridge chickens. In liver, the highest expression level of IGF1R was detected on 21 d in Guangxi partridge chickens, significantly higher than those on E9 d, E12 d, E16 d and 0 d; while the highest level was found on 63 d and significantly higher than those on the other studied development stages. IRS1 mRNA could also be detected at the whole studied stages in skeletal muscles and liver of both chicken breeds. In skeletal muscles, expression of IRS1 were higher on E9 d or E12 d than any other age, and then decreased with age and kept relative low level during PH development in both breeds. The liver IRS1 expression pattern was consistent with IGF1R in both breeds. Significant positive relationships were observed for the expression of studied genes in BM, LM and liver tissues of both chicken breeds. Meanwhile, the skeletal muscle expression of these three genes were all showed significant negative relationships with body weight and breast (leg) muscle weight, whereas the liver expression of these three genes were all showed significant positive relationships with body weight, breast (leg) muscle weight and liver weight. 【Conclusion】These results implied that the expression of selected genes that comprise the IGF1-PI3K-Akt pathway existed identical trends, and differential expression between breeds and tissues might be one of the main reasons for the different growth rate of the different types of yellow feather broiler.

Key words: yellow feather broiler, gene expression, IGF1-PI3K-Akt pathway, skeletal muscle, liver

Table 1

Gene-specific primers for quantitative RT-PCR"

基因名称
Gene name
引物序列
Primer sequence
PCR条件
PCR conditions (℃)
IGF1 5′ primer: AGCTGGTTGATGCTCTTCAGTTCGT 60
3′ primer: TCCTCAGGTCACAACTCTGGAAGC
IGF1R 5′ primer: TTCAGGAACCAAAGGGCGA 55
3′ primer: TGTAATCTGGAGGGCGATACC
IRS1 5′ primer: CTACCGCCTGTGCCTGACTAAC 60
3′ primer: CGTCCCACCTCGATGAAGAAG
HSP70 5′ primer: TCTGCTCCTGTTGGATGTC 60
3′ primer: TGGGAATGGTGGTGTTACG

Fig. 1

The profiles of body weight, breast muscle weight, thigh muscle weight and liver weight during growth stages in different chicken breeds A: Body weight; B: Breast muscle weight; C: Leg muscle weight; D: Liver weight. ed indicates embryonic days, and d indicates age after hatching. Bar diagram values with the same letter are not significantly different between different age (P>0.05), and values with the different letters are significantly different between different ages (P<0.05). Superscript * indicates significantly different between two breeds in the same age at the level of 0.05, and superscript ** indicates significantly different between two breeds in the same age at the level of 0.01"

Table 2

The relative expression level of IGF1, IGF1R and IRS1 in skeletal muscles and liver of Huashan and Guangxi partridge chickens at different developmental stages"

基因Gene 组织Tissue 品种
Breed
9 ed 12 ed 16 ed 0 d 7 d 21 d 35 d 49 d 63 d
IGF1 胸肌
Breast
GXMJ 9.65±1.06 a 9.78±0.37a 5.18±1.07b 1.51±0.33 c 0.27±0.08d 0.19±0.05d 0.14±0.03d 0.06±0.005e 0.05±0.005e
HSMJ 1.12±0.18b** 1.92±0.26a** 0.98±0.26b** 0.42±0.07c* 0.24±0.08c 0.18±0.05c 0.17±0.03c 0.13±0.04c 0.05±0.004d
腿肌
Leg
GXMJ 54.92±2.51a 54.77±5.06a 33.20±3.39 b 1.32±0.39c 2.08±0.37cd 2.86±0.44d 2.51±0.48cd 3.42±0.85d 1.58±0.16c
HSMJ 10.44±1.5a** 10.31±0.2a** 1.77±0.20b** 0.26±0.65c* 2.74±0.57d 1.53±0.26b 3.79±0.86d 2.25±0.42b 1.06±0.18b
肝脏
Liver
GXMJ 0 0 0 1.23±0.23c 4.02±1.07c 57.62±6.46a 47.84±5.54a 52.47±7.05a 29.81±3.59b
HSMJ 0.04±0.01e* 0.22±0.02d* 0.31±0.04d 3.02±0.52c* 5.11±1.47c 66.06±6.99b* 74.44±9.4ab* 80.87±12.0a* 79.71±9.1a**
IGF
1R
胸肌
Breast
GXMJ 3.50±0.23 a 1.64±0.15b 2.63±0.33b 1.32±0.33 c 0.06±0.01d 0.08±0.01d 0.10±0.02d 0.03±0.00d 0.04±0.00d
HSMJ 0.45±0.07a** 0.24±0.04b** 0.25±0.06b** 0.17±0.07bc* 0.02±0.00c 0.02±0.00c 0.05±0.00c 0.03±0.00c 0.01±0.00c
腿肌
Leg
GXMJ 6.14±0.86a 4.21±0.56b 2.31±0.37c 1.18±0.28d 0.46±0.08d 0.37±0.05d 0.49±0.05d 0.30±0.04d 0.21±0.06d
HSMJ 1.24±0.23a** 1.21±0.27a* 0.18±0.05b** 0.10±0.01b** 0.17±0.02b 0.12±0.02b 0.29±0.06b 0.17±0.02b 0.17±0.01b
肝脏
Liver
GXMJ 0.15±0.02c 0.16±0.02 c 0.37±0.03c 0.96±0.06b 1.62±0.19ab 1.96±0.27a 1.48±0.16ab 1.54±0.19ab 1.35±0.28ab
HSMJ 0.21±0.05d 0.36±0.04d 0.50±0.03d 1.21±0.18c 1.77±0.23bc 1.78±0.30bc 1.88±0.24bc 2.60±0.35b* 5.74±0.91a*
IRS1 胸肌
Breast
GXMJ 2.07±0.09a 1.69±0.12a 1.51±0.16a 1.50±0.13a 0.17±0.02b 0.30±0.06b 0.37±0.03b 0.22±0.03b 0.21±0.02b
HSMJ 0.56±0.05a** 0.39±0.03a* 0.31±0.02a* 0.55±0.06a* 0.09±0.01c 0.16±0.01b 0.21±0.03b 0.13±0.04b 0.02±0.00c*
腿肌
Leg
GXMJ 5.84±0.59a 4.32±0.49b 1.93±0.11c 1.51±0.04cd 0.79±0.06cd 1.07±0.13cd 0.90±0.10cd 0.80±0.06cd 0.61±0.05d
HSMJ 2.08±0.26a** 2.28±0.54a* 0.63±0.10b* 0.73±0.04b* 0.26±0.04b* 0.40±0.06b* 0.60±0.09b 0.48±0.07b 0.38±0.04b
肝脏
Liver
GXMJ 0.09±0.00c 0.22±0.04c 0.10±0.01c 0.92±0.20b 1.80±0.27ab 3.08±0.46a 2.84±0.55a 3.02±0.74a 2.63±0.22a
HSMJ 0.08±0.00f 0.11±0.01f 0.08±0.01f 0.76±0.13e 1.52±0.11e 2.58±0.15d 3.53±0.53c 6.29±0.73b* 16.05±2.01a**

Table 3

Correlations betweenIGF1-PI3K-AKT signaling pathway genes in skeletal muscles and liver of the two chicken breeds"

参数
Parameters
广西麻鸡Guangxi Partridge 花山麻鸡Huashan Partridge
IGF1R IRS1 IGF1R IRS1
胸肌
Breast muscle
IGF1 0.851** 0.641** 0.418** 0.457**
IRS1 0.806** 0.648**
腿肌
Leg muscle
IGF1 0.884** 0.873** 0.719** 0.670**
IRS1 0.854** 0.884**
肝脏
Liver
IGF1 0.494** 0.682** 0.489** 0.389**
IRS1 0.759** 0.911**

Table 4

Correlations between the expression of IGF1-PI3K-AKT signaling pathway genes and growth traits in the two chicken breeds"

组织
Tissue
参数
Parameters
广西麻鸡Guangxi Partridge 花山麻鸡Huashan Partridge
IGF1 IGF1R IRS1 IGF1 IGF1R IRS1
胸肌
Breast muscle
体重Body weight
-0.453** -0.537** -0.467** -0.519* -0.430** -0.594**
胸肌重Breast weight -0.405** -0.483** -0.424** -0.441** -0.361** -0.542**
腿肌
Leg muscle
体重Body weight -0.413** -0.471** -0.451** -0.389** -0.332** -0.370**
腿肌重Leg weight -0.377** -0.435** -0.417** -0.362** -0.284* -0.321**
肝脏
Liver
体重Body weight 0.369* 0.965** 0.817** 0.693** 0.781** 0.817**
肝脏重Liver weight 0.458** 0.409** 0.851** 0.601** 0.794** 0.851**
胸肌重Breast weight 0.352** 0.453** 0.783** 0.563** 0.696** 0.752**
腿肌重Leg weight 0.365** 0.483** 0.812** 0.598** 0.723** 0.795**
[1] 王志祥. 固始鸡与肉鸡、蛋鸡肉质、生长、代谢及相互关系的比较研究[D]. 北京: 中国农业大学, 2004.
WANG Z X. Comparison studies on meat quality, growth, metabolism and relationships among Gushi, broiler and layer chicks[D]. Beijing: China Agricultural University, 2004. (in Chinese)
[2] 周大薇. 矮小型与正常型鸡体型性状和内脏器官发育的比较研究. 四川畜牧兽医, 2013,276(9):17-19.
ZHOU D W. Comparison and investigation on the body type traits and development of internal organs between dwarf chicken and ordinary chicken. Sichuan Animal & Veterinary Sciences, 2013,276(9):17-19. (in Chinese)
[3] SCHIAFFINO S, MAMMUCARI C. Regulation of skeletal muscle growth by the IGF1-Akt/ PKB pathway: insights from genetic models. Skeletal Muscle, 2011,1:4.
[4] SCHIAFFINO S, DYAR KA, CICILIOT S, BLAAUW B, SANDRI M. Mechanisms regulating skeletal muscle growth and atrophy. FEBS Journal, 2013,280(17):4294-4314. https://doi.org/10.1111/febs.12253.
[5] TILLEY R E, MCNEIL C J, ASHWORTH C J, PAGE K R, MCARDLE H J. Altered muscle development and expression of the insulin-like growth factor system in growth retarded fetal pigs. Domestic Animal Endocrinology, 2007,32(3):167-177.
[6] AGROGIANNIS G D, SIFAKIS S, PATSOURIS E S, KONSTANTINIDOU A E. Insulin-like growth factors in embryonic and fetal growth and skeletal development (Review). Molecular Medicine Reports, 2014,10(2):579-584.
[7] WANG Y, BAI X J, WANG Z X, CAO J, DONG Y L, DONG Y J, CHEN Y X. Various led wavelengths affected myofiber development and satellite cell proliferation of chick embryos via the IGF-1 signaling pathway. Photochemistry and Photobiology, 2017,93(6):1492-1501.
[8] JONES J I, CLEMMONS D R. Insulin-like growth factors and their binding proteins: biological actions. Endocrine Reviews, 1995,16(1):3-34.
[9] WEEKS K L, BERNARDO B C, OOI JENNY Y Y, PATTERSON N L, MCMULLEN J R. The IGF1-PI3K-Akt signaling pathway in mediating exercise-induced cardiac hypertrophy and protection. Advances in Experimental Medicine and Biology, 2017,1000:187-210.
[10] VALENTINIS B, ROMANO G, PERUZZI F. Growth and differentiation singnal by the insulin like growth factor binding I receptor in hemopoietic cells are mediated through different pathways. Journal of Biological Chemistry, 1999,274(18):12423-12430.
[11] KALISTA S O, SCHAKMAN H G, LAUSE B P. The type 1 insulin-like growth factor receptor (IGF-IR) Pathway is mandatory for the follistatin-induced skeletal muscle hypertrophy. Endocrinology, 2012,153:241-253.
[12] BELFORE A, FRASCA F, PANDINI G, SCIACCA L, VIGNERI R. Insulin receptor isoforms and insulin receptor/insulin-like growth factor receptor hybrids in physiology and disease. Endocrine Reviews, 2009,30(6):586-623.
[13] MAVALLI M D, DIGIROLAMO D J, FAN Y, RIDDLE R C, CAMPBELL K S, VAN GROEN T, FRANK S J, SPERLING M A, ESSER K A, BAMMAN M M. Distinct growth hormone receptor signaling modes regulate skeletal muscle development and insulin sensitivity in mice. Journal of Clinical Investigation, 2010,120:4007-4020.
[14] DONG X C, PARK S, LIN X Y, KYLE C, YI X J, WHITE M F. Irs1 and Irs2 signaling is essential for hepatic glucose homeostasis and systemic growth. Journal of Clinical Investigation, 2006,116(1):101-114.
[15] TAMEMOTO H, KADOWAKI T, TOBE K, SAKURA H, HAYAKAWA T, TERAUCHI Y, UEKI K, KABURAGI Y, SATOH S. Insulin resistance and growth retardation in mice lacking insulin receptor substrate-1. Nature, 1994,372(6502):182-186.
[16] LI Z H, CAI B L, ABDALLA B A, ZHU X N, ZHENG M, HAN P G, NIE Q H, ZHANG X Q. LncIRS1 controls muscle atrophy via sponging miR-15 family to activate IGF1-PI3K/AKT pathway. Journal of Cachexia, Sarcopenia and Muscle, 2019, DOI: 10.1002/jcsm.12374.
doi: 10.1002/jcsm.12374
[17] 盛中伟, 姬改革, 刘一帆, 巨晓军, 单艳菊, 邹剑敏, 章明, 屠云洁, 束婧婷. 鸡生长发育早期骨骼肌IGF1R mRNA表达规律研究. 浙江农业学报, 2020,32(7):1160-1165.
SHENG Z W, JI G G, LIU Y F, JU X J, SHAN Y J, ZOU J M, ZHANG M, TU Y J, SHU J T. Study on mRNA expression pattern of IGF-1R gene in chicken skeletal muscles during early development. Acta Agriculturae Zhejiangensis, 2020,32(7):1160-1165. (in Chinese)
[18] 陈伟. 孵化后期外源二糖和谷氨酰胺调控肉鸭骨骼肌蛋白质代谢机制研究[D]. 武汉: 华中农业大学, 2010.
CHEN W. Study on the regulatory role of administrating exogenous disaccharide and glutamine to late-term duck embryos in affecting the protein metabolism in skeletal muscle[D]. Wuhan: Huazhong Agricultural University, 2010. (in Chinese)
[19] CHEN W, TANGARA M, XU J, PENG J. Developmental transition of pectoralis muscle from atrophy in late-term duck embryos to hypertrophy in neonates. Experimental Physiology, 2012,97(7):861-872.
[20] 束婧婷, 朱文奇, 单艳菊, 陈文峰, 徐文娟, 胡艳, 宋迟, 李慧芳, 王金玉. 胰岛素样生长因子系统基因在不同鸭种发育早期肝和肌肉中的表达. 畜牧兽医学报, 2014,45(2):183-190.
SHU J T, ZHU W Q, SHAN Y J, CHEN W F, XU W J, HU Y, SONG C, LI H F, WANG J Y. Expression of insulin-like growth factor system genes in liver and breast muscle tissue during early development of different duck breeds. Acta Veterinaria et Zootechnica Sinica, 2014,45(2):183-190. (in Chinese)
[21] MOORE D T, FERKET P R, MOZDZIAK P E. Muscle development in the late embryonic and early post-hatch poultry. International Journal of Poultry Science, 2005,4(3):138-142.
[22] 邢海权, 闫梦菲. 2011. 胰岛素样生长因子 IGF-1 的研究进展. 畜禽业, 2011,8:36-37.
XING H Q, YAN M F. Progress in research on insulin-like growth factor IGF-1. Livestock and Poultry Industry, 2011,8:36-37. (in Chinese)
[23] ROMMEL C, BODINE S C, CLARKE B A, ROSSMAN R, NUNEZ L, STITT T N, YANCOPOULOS G D, GLASS D J. Mediation of IGF-1- induced skeletal myotube hypertrophy by PI(3)K/Akt/mTOR and PI(3)K/Akt/GSK3 pathways. Nature Cell Biology, 2001,3:1009-1013.
[24] 束婧婷, 宋迟, 徐文娟, 章明, 单艳菊, 陈文峰, 宋卫涛, 陶志云, 李慧芳. IGF-I-CaN-NFATc3信号通路相关基因在鸭发育早期骨骼肌中的同步表达规律及其与肌纤维性状的相关性. 中国农业科学, 2015,48(6):1195-1204.
SHU J T, SONG C, XU W J, ZHANG M, SHAN Y J, CHEN W F, SONG W T, TAO Z Y, LI H F. Expression profile of IGF-I- calcineurin-NFATc3-dependent pathway genes in skeletal muscles and their associations with myofiber traits during embryonic and early post-hatching development in ducks. Scientia Agricultura Sinica, 2015,48(6):1195-1204. (in Chinese)
[25] 蒋明雅, 邹小利, 罗文, 张细权. 不同生长速度型鸡胚胎发育后期肌纤维形态学对比分析. 中国家禽, 2017,39(16):10-16.
JIANG M Y, ZOU X L, LUO W, ZHANG X Q. Skeletal muscle fiber morphological comparative study in chickens with different growth rate during the late embryonic development. China Poultry, 2017,39(16):10-16. (in Chinese)
[26] KIKUCHI K, BUONOMO F C, KAJIMOTO Y, ROTWEIN P. Expression of insulin-like growth factor-I during chicken development. Endocrinology, 1991,128(3):1323-1328.
[27] DUPONT J, HOLZENBERGER M. Biology of insulin-like growth factors in development. Birth Defects Research (Part C), 2003,69:257-271.
[28] CARTER A M, KINGSTON M J, HAN K K, MAZZUCA D M, NYGARD K, HAN V K M. Altered expression of IGFs and IGF-binding proteins during intrauterine growth restriction in guinea pigs. Journal of Endocrinology, 2005,184:179-189.
[29] RONDINONE C M, WANG L M, LONNROTH P, WESSLAU C, PIERCE J H, SMITH U. Insulin receptor substrate (IRS) 1 is reduced and IRS-2 is the main docking protein for phosphatidylinositol 3-kinase in adipocytes from subjects with non-insulin-dependent diabetes mellitus. Proceedings of the National Academy of Sciences USA, 1997,94(8):4171-4175.
[30] 荣华, 豆腾飞, 张丽春, 李丽红, 万全书, 何昌明, 赵平, 葛长荣, 刘丽仙, 赵素梅, 李琦华, 贾俊静. 大围山微型鸡IGF-1基因表达量与生长性状的相关性分析. 中国家禽, 2015,37(4):5-8.
RONG H, DOU T F, ZHANG L C, LI L H, WAN Q S, HE C M, ZHAO P, GE C R, LIU L X, ZHAO S M, LI Q H, JIA J J. Correlation analysis on IGF-1 gene expression and growth traits in Daweishan Mini Chicken. China Poultry, 2015,37(4):5-8. (in Chinese)
[1] SHEN LongXian, WANG LiTing, HE Ke, DU Xue, YAN FeiFei, CHEN WeiHu, LÜ YaoPing, WANG Han, ZHOU XiaoLong, ZHAO AYong. Effects of Melatonin and Nicotinamide Mononucleotides on Proliferation of Skeletal Muscle Satellite Cells in Goose [J]. Scientia Agricultura Sinica, 2023, 56(2): 391-404.
[2] GU LiDan,LIU Yang,LI FangXiang,CHENG WeiNing. Cloning of Small Heat Shock Protein Gene Hsp21.9 in Sitodiplosis mosellana and Its Expression Characteristics During Diapause and Under Temperature Stresses [J]. Scientia Agricultura Sinica, 2023, 56(1): 79-89.
[3] ZHANG KeKun,CHEN KeQin,LI WanPing,QIAO HaoRong,ZHANG JunXia,LIU FengZhi,FANG YuLin,WANG HaiBo. Effects of Irrigation Amount on Berry Development and Aroma Components Accumulation of Shine Muscat Grape in Root-Restricted Cultivation [J]. Scientia Agricultura Sinica, 2023, 56(1): 129-143.
[4] YANG XinRan,MA XinHao,DU JiaWei,ZAN LinSen. Expression Pattern of m6A Methylase-Related Genes in Bovine Skeletal Muscle Myogenesis [J]. Scientia Agricultura Sinica, 2023, 56(1): 165-178.
[5] LAI ChunWang, ZHOU XiaoJuan, CHEN Yan, LIU MengYu, XUE XiaoDong, XIAO XueChen, LIN WenZhong, LAI ZhongXiong, LIN YuLing. Identification of Ethylene Synthesis Pathway Genes in Longan and Its Response to ACC Treatment [J]. Scientia Agricultura Sinica, 2022, 55(3): 558-574.
[6] SHU JingTing,SHAN YanJu,JI GaiGe,ZHANG Ming,TU YunJie,LIU YiFan,JU XiaoJun,SHENG ZhongWei,TANG YanFei,LI Hua,ZOU JianMin. Relationship Between Expression Levels of Guangxi Partridge Chicken m6A Methyltransferase Genes, Myofiber Types and Myogenic Differentiation [J]. Scientia Agricultura Sinica, 2022, 55(3): 589-601.
[7] GUO ShaoLei,XU JianLan,WANG XiaoJun,SU ZiWen,ZHANG BinBin,MA RuiJuan,YU MingLiang. Genome-Wide Identification and Expression Analysis of XTH Gene Family in Peach Fruit During Storage [J]. Scientia Agricultura Sinica, 2022, 55(23): 4702-4716.
[8] KANG Chen,ZHAO XueFang,LI YaDong,TIAN ZheJuan,WANG Peng,WU ZhiMing. Genome-Wide Identification and Analysis of CC-NBS-LRR Family in Response to Downy Mildew and Powdery Mildew in Cucumis sativus [J]. Scientia Agricultura Sinica, 2022, 55(19): 3751-3766.
[9] YuXia WEN,Jian ZHANG,Qin WANG,Jing WANG,YueHong PEI,ShaoRui TIAN,GuangJin FAN,XiaoZhou MA,XianChao SUN. Cloning, Expression and Anti-TMV Function Analysis of Nicotiana benthamiana NbMBF1c [J]. Scientia Agricultura Sinica, 2022, 55(18): 3543-3555.
[10] MingJie XING,XianHong GU,XiaoHong WANG,Yue HAO. Effects of IL-15 Overexpression on Myoblast Differentiation of Porcine Skeletal Muscle Cells [J]. Scientia Agricultura Sinica, 2022, 55(18): 3652-3663.
[11] JIN MengJiao,LIU Bo,WANG KangKang,ZHANG GuangZhong,QIAN WanQiang,WAN FangHao. Light Energy Utilization and Response of Chlorophyll Synthesis Under Different Light Intensities in Mikania micrantha [J]. Scientia Agricultura Sinica, 2022, 55(12): 2347-2359.
[12] YUAN JingLi,ZHENG HongLi,LIANG XianLi,MEI Jun,YU DongLiang,SUN YuQiang,KE LiPing. Influence of Anthocyanin Biosynthesis on Leaf and Fiber Color of Gossypium hirsutum L. [J]. Scientia Agricultura Sinica, 2021, 54(9): 1846-1855.
[13] ZHAO Ke,ZHENG Lin,DU MeiXia,LONG JunHong,HE YongRui,CHEN ShanChun,ZOU XiuPing. Response Characteristics of Plant SAR and Its Signaling Gene CsSABP2 to Huanglongbing Infection in Citrus [J]. Scientia Agricultura Sinica, 2021, 54(8): 1638-1652.
[14] ZHAO Le,YANG HaiLi,LI JiaLu,YANG YongHeng,ZHANG Rong,CHENG WenQiang,CHENG Lei,ZHAO YongJu. Expression Patterns of TETs and Programmed Cell Death Related Genes in Oviduct and Uterus of Early Pregnancy Goats [J]. Scientia Agricultura Sinica, 2021, 54(4): 845-854.
[15] ZHU FangFang,DONG YaHui,REN ZhenZhen,WANG ZhiYong,SU HuiHui,KU LiXia,CHEN YanHui. Over-expression of ZmIBH1-1 to Improve Drought Resistance in Maize Seedlings [J]. Scientia Agricultura Sinica, 2021, 54(21): 4500-4513.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!